Frequently asked questions
Heart failure (HF), sometimes called congestive heart failure (CHF) occurs when the heart muscles become weak or damaged and can no longer pump blood efficiently or cannot relax sufficiently to allow blood to flow back into the heart from the lungs. This can be the result of previous heart attacks or high blood pressure (hypertension) and since people now live longer with these conditions, the number of people with heart failure is on the rise. It is estimated that there are about 600,000 Canadians currently living with heart failure.
HF is characterized by specific symptoms such as shortness of breath and fatigue, and signs such as fluid retention and swelling (edema). Although there is no cure, there are treatments and lifestyle changes which can help improve the condition and quality of life. These include exercising, reducing salt in your diet, reducing stress and losing weight, (1, 2)
Certain herbal supplements and non-prescription products can be risky with heart failure and should be avoided. These include:
- Effervescent (dissolving) tablets which contain over 500mg of sodium per tablet. Some examples are: Alka Seltzer, Eno fruit salts, Redoxon (effervescent Vitamins C & B, calcium). Always check labels for sodium content. (3)
- Licorice root. When used in amounts commonly found in foods, licorice has Generally Recognized as Safe (GRAS) status in the US. However, eating licorice daily for several weeks or longer can cause severe adverse effects including high blood pressure, low potassium, changes in heart rate and even heart attack in otherwise healthy people. Although consuming 20 grams or more licorice daily is more likely to cause these effects, smaller amounts have also caused problems when taken long-term for months to years. (4)
- Aconite or Wolfsbane. Aconite root contains toxic compounds that are strong, fast-acting poisons that affect the heart and central nervous system, causing paralysis and death. All species of this plant are dangerous. Aconite can cause nausea, vomiting, dizziness, muscle spasms, hypothermia, paralysis of respiratory system, and heart rhythm disorders. It can also be absorbed through the skin in amounts sufficient to cause poisoning.
- Hawthorne. Hawthorne is often found in combination products recommended for the heart. It may reduce blood pressure and decrease heart rate, but it can interact with other medications used in heart failure and its use is not recommended. (4)
- St. John’s wort. When St. John’s wort is used with digoxin (Toloxin®), a common prescription treatment for some types of heart failure, it can decrease blood levels and therapeutic effects of digoxin. St. John's wort can reduce digoxin levels by 25% after 10 days in healthy people. Its use should be avoided in heart failure. (5)
- Yohimbine. Yohimbine is a prescription drug in Canada and should be used only under the supervision of a health care professional. The use of products containing yohimbine can result in serious adverse reactions, particularly in people with high blood pressure, or heart, kidney or liver disease. Side effects associated with yohimbine include increased blood pressure and heart rate, anxiety, dizziness, tremors, headache, nausea and sleep disorders. (4)
- Other herbal supplements that can affect heart rate and should be avoided include: green tea, lily-of-the-valley and motherwort.
- Supplements that can interact with other drugs used to treat HF and that should be avoided include: danshen, black cohosh, dong quai, garlic, ginkgo, ginseng, gossypol and saw palmetto. (3, 5)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
medSask, October 2016
1. Heart and Stroke Foundation of Canada. Heart Failure. Available at http://www.heartandstroke.com/site/c.ikIQLcMWJtE/b.3484065/k.9224/Heart_failure.htm. Accessed October 2016.
2. Mayo Clinic. Heart Failure. Availablet at http://www.mayoclinic.org/diseases-conditions/heart-failure/basics/definition/con-20029801. Accessed October 2016.
3. Professional Resource, Medications and Supplements with Adverse Effects in Heart Failure. Pharmacist’s Letter/Prescriber’s Letter. September 2016.
4. Health Canada. Five unauthorized products seized from Keebo Sports Supplements in Winnipeg may pose serious health risks. Available at http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/60456a-eng.php. Accessed October 2016.
5. Natural Medicines Comprehensive Database. Available by subscription at http://naturaldatabase.therapeuticresearch.com
Q. Are teeth whiteners safe to use? Does a whitening toothpaste work just as well?
The decision to whiten teeth should only be made after consulting a dentist. The options for whitening range from toothpastes that contain whiteners to at-home whitening products to dentist-office bleaching treatments. The products you can buy without a prescription are generally safe when used as directed and for the suggested amount of time.
Teeth may appear less than white because of surface stains or because the dentin layer below the outer enamel is not white. Since the enamel is translucent and the dentin layer is varying shades of yellow, it will affect the appearance of the teeth. Coffee, tea, red wine, sports drinks, hard candy, berries and tomato sauce are all foods that can cause tooth discoloration. (1, 2)
Some common ingredients in tooth whitening pastes include peroxide, calculus control agents called pyrophosphates, and polishing substances such as silica and baking soda. (3) The effects of whitening toothpastes usually are not dramatic. They can’t change the natural color of your teeth or lighten a stain that goes deeper than a tooth’s surface. Removing deeper stains and changing the color of the internal tooth structure requires a bleaching product. When used twice a day, whitening toothpaste takes about two to six weeks to whiten the teeth. (1, 2)
Dental Bleaching Products
Over the counter (OTC) dental bleaching products usually contain hydrogen peroxide. (3) For most people, bleaching is safe, easy, and inexpensive. Hydrogen peroxide–impregnated polyethylene whitening strips can be used at home to bleach teeth or to maintain already whitened teeth. With darker stains, the best results are achieved by using a combination of dental office and home bleaching systems. Most patients will require periodic re-treatment.
The most common adverse effect of these bleaching products is sensitivity. Approximately two thirds of patients have short-term, minor tooth sensitivity to cold and may also have gum irritation. Tooth surfaces, especially exposed roots or enamel surfaces with defects, are porous and are more likely to develop cold sensitivity. (4)
None of the teeth whitening options currently available are permanent. Food, drink and aging, will cause your teeth to darken again. Whatever whitening method chosen, eventually you will need to repeat the process if you want to maintain the whiteness of your teeth long-term. (1)
1. Sheridan P. Dental Specialties, Mayo Clinic, Rochester, Minn. Available at http://newsnetwork.mayoclinic.org/discussion/mayo-clinic-q-and-a-many-safe-choices-available-to-help-whiten-teeth/. Accessed Sept. 2016.
2. Canadian Pharmacists’ Letter. PL Detail-Document. A Look at Tooth Whiteners. Pharmacist’s Letter/Prescriber’s Letter. December 2013.
3. Plaque and tartar control. In: Dentalcare.com. Available at http://www.dentalcare.com/en-US/dental-education/patient-education/plaque-english.aspx. Accessed Sept. 2016.
4. Patel D. Tooth Discoloration Treatment & Management. In: Medscape online. Available at http://emedicine.medscape.com/article/1076389-treatment. Accessed Sept. 2016.
Resistance to the most commonly used treatments for head lice appears to be emerging in Canada. Although a 1% permethrin creme rinse (e.g. Nix, Kwellada-P) or a pyrethrin shampoo (e.g. R & C Shampoo) is still recommended as first-line treatment, alternative products such as dimeticone and isopropyl myristate are proving to be as or in some cases more effective if they are used properly according to the package directions. These products can be considered if resistance to first line treatments is a known problem in your location, if first line treatment fails (live lice in hair 48 hours after treatment), or if you have concerns about using insecticides on young children. (1)
Dimeticone (e.g. NYDA) is reported to be a successful non-insecticide approach to lice infestations. It is a silicone-based product which when sprayed on dry hair, flows into the breathing system of lice, then thickens and suffocates the lice. According to two studies, more subjects treated with dimeticone were lice free nine days after treatment than those who were treated with permethrin.
Another product, isopropyl myristrate (Resultz), dissolves the outer skeletons of lice and appears to be at least as effective as insecticides. (1, 2)
Dimeticone and isopropyl myristrate are well tolerated and no serious side effects have been reported. Because of the way these products work, it is hoped that lice will be less likely to become resistant to them. (3)
No matter which treatment is chosen, using a nit comb to remove eggs from the hair shafts after treatment is still necessary to prevent recurrences.
Several other remedies including enzymes which are claimed to affect the outer skeleton of the lice and cause premature molting and death are advertised for treatment of head lice. There is no evidence in the scientific literature to support these claims. These products are advertised as non-toxic to humans, but caution is advised especially if there is not full disclosure of all product ingredients. (4)
For an overview of head lice and its treatment go to: https://www.saskatchewan.ca/residents/health/accessing-health-care-services/healthline and enter “lice” in the search field.
Prepared by Jean Macpherson, BSP; reviewed by Karen Jensen MSc, BSP
medSask, September 2016
- Canadian Pharmacist’s Letter - PL Detail-Document, Non-insecticide Lice Treatments. Pharmacist’s Letter/Prescriber’s Letter. April 2012.
- Kolber M, Pierse M, Nickonchuk T. The louse is (no longer) in the house. Canadian Family Physician. Tools for Practice. Vol 62: April• 2016.
- Dumont Z, Rutherford L. Head lice: Picking out truth from myth Pharmacy Practice 2012;28:18.
- Head lice control. On: Beyond Pesticides website. Available at https://www.beyondpesticides.org/assets/media/documents/alternatives/factsheets/Head%20Lice%20Control2.pdf . Accessed August 2016.
Q. What foods will prevent Alzheimer’s disease? I’ve heard there is a special diet.
Recent studies give more weight to the suggestion that what we eat can affect our brains. Once a brain disorder such as Alzheimer’s disease (AD) is diagnosed, effective treatments are limited at best. It would therefore make sense that preventing or at least delaying the onset would be preferred.
Improving cardiovascular (heart) health may reduce the risk of dementia. Diets that are high in plant-based foods and oils that are low in saturated fats have been associated with a variety of health benefits, including lowering the risk of heart disease. One diet that features this pattern of eating and these types of food is the Mediterranean diet. Conclusive evidence however, of the beneficial effect of diet on dementia is lacking. (1)
The Mediterranean diet emphasizes:
- Eating primarily plant-based foods, such as fruits and vegetables, whole grains, legumes and nuts
- Replacing butter with healthy fats such as olive oil and canola oil
- Using herbs and spices instead of salt to flavor foods
- Limiting red meat to no more than a few times a month
- Eating fish and poultry at least twice a week (1,2)
It appears that specific areas of the brains of people with Alzheimer’s disease and other dementias are smaller than those of people who not affected by these diseases. Magnetic resonance imaging (MRI) scans have shown there is a correlation between an increase in the severity of dementia and a decrease in the size of the whole brain and the thickness of specific areas of the brain such as the cerebral cortex. The cortical area of the brain plays a key role in memory, attention, perception, awareness, thought, language, and consciousness. (3)
A study of MRI scans that measured these areas of the brain in elderly participants showed that people who had followed a Mediterranean style diet and taken supplemental B vitamins, had wider measurements than those who ate less beneficial foods with higher percentages of calories from carbohydrates and sugar. The difference between the brain matter in the two groups is equal to about five years of aging.
These findings suggest that a healthy diet that is high in fish and vegetables is associated with larger cortical thickness in several brain regions and might help us maintain brain function and delay the onset of dementia disorders. (4, 5)
There are other things you can do that may keep your brain and heart healthy. As more is understood about what role these factors play in Alzheimer’s disease risk, health experts recommend that all adults:
- exercise regularly
- eat a healthy diet rich in fruits and vegetables
- engage in social and intellectually stimulating activities
- control type 2 diabetes
- lower high blood pressure levels
- lower high blood cholesterol levels
- maintain a healthy weight
- stop smoking
- get treatment for depression
Although scientists do not yet know for sure if these healthy habits can directly prevent or delay Alzheimer’s disease, it’s important to note that these habits have many benefits for overall health and well-being. (1, 6)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
medSask, August 2016
- Press, D, Alexander, M, Prevention of dementia. In UpToDate online database. Available at www.uptodate.com (with subscription). Literature review current through: Jul 2016. This topic last updated: Mar 16, 2016. Accessed August 2016.
- Mayo Clinic Staff. Patient Care and Health Information. Mediterranean diet: A heart-healthy eating plan. In Mayo clinic online. Available at:http://www.mayoclinic.org/healthy-lifestyle/nutrition-and-healthy-eating/in-depth/mediterranean-diet. Accessed August 2016.
- Kiho I et al. Variations in cortical thickness with dementia severity in Alzheimer's disease. Neuroscience Letters. Volume 436, Issue 2, 9 May 2008, Pages 227–231. Available at http://www.sciencedirect.com/science/article/pii/S0304394008003388.
- Brooks M. Mediterranean Diet Linked to Larger Brain Volume. Medscape Medical News - Neurology. October 22, 2015. Available at http://www.medscape.com/viewarticle/853114 .
- National Institute on Aging. Preventing Alzheimer’s Disease: What do we know. Available at https://www.nia.nih.gov/alzheimers/publication/preventing-alzheimers-disease/so-what-can-you-do . Accessed August 2016.
- National Institute on Aging. Preventing Alzheimer’s Disease: What do we know. Available at https://www.nia.nih.gov/alzheimers/publication/preventing-alzheimers-disease/so-what-can-you-do . Accessed August 2016.
Gout is a type of arthritis that causes severe pain, redness, warmth and swelling in joints. It is caused by a build-up of uric acid crystals in the blood. In people with gout, the body doesn’t get rid of uric acid as quickly as in people who don’t have gout. Uric acid is a chemical produced when the body breaks down substances called purines. Purine occurs naturally in the body, but certain foods can increase uric acid levels either because they contain relatively high amounts of purines or because they interfere with the uric acid elimination process.
Gout attacks occur most often at night and usually affect a single joint such as the base of the big toe or the knee. Men are more likely to get gout at a younger age, but it becomes increasingly common in women after menopause. Fortunately, gout is treatable, and there are ways to reduce the risk that attacks will recur. (1, 2)
The period after an attack of gout has cleared up is called the intercritical period. The time between episodes varies, but most untreated people will have a second attack within 2 years.
Prevention of a recurrence can be aided by addressing some lifestyle changes during the intercritical period. These might include identifying causes of increased uric acid (hyperuricemia) such as food choices, alcohol consumption, body weight and also management of any health issues such as high blood pressure, diabetes, high cholesterol, kidney disease and heart disease. Medications which lower uric acid (for example, allopurinol) and anti-inflammatory medications (for example, naproxen or indomethacin) may also be used during this time to help decrease the likelihood of another attack. (3)
Gout has been associated for centuries with overindulgence in meats, seafood and alcohol. In the past, the recommended diet focused on eliminating all foods that had moderate to high amounts of purine. The list of foods to avoid was long, which made the diet difficult to follow. More recent research has shown a clearer picture of the role of diet in gout management. Some, but not all, foods with purines should be eliminated. Other foods can be included in your diet to help control uric acid levels.
The general principles of a gout diet are the same as those for a balanced, healthy diet.
Although diet isn't likely to lower the uric acid concentration in the blood enough to treat gout without medication, it may help decrease the number of attacks and limit their severity. In general, losing weight lowers the risk of gout and reduces stress on joints.
- Eat more fruits, vegetables and whole grains, which provide complex carbohydrates. Studies show that vegetables high in purines do not increase the risk of gout attacks. A diet based on lots of fruits and vegetables can include high-purine vegetables, such as asparagus, spinach, peas, cauliflower or mushrooms. Beans or lentils, which are moderately high in purines, are acceptable and a good source of protein.
- Add protein with low-fat or fat-free dairy products, such as low-fat yogurt or skim milk. These are associated with reduced uric acid levels.
- Limit daily proteins from lean meat, fish and poultry to 4 to 6 ounces (113 to 170 grams).
- Cut back on saturated fats from red meats, fatty poultry and high-fat dairy products.
- Include 8 to 16 cups (2 to 4 litres) of fluids a day with at least half of that as water. Coffee (regular caffeinated) consumption in moderation may help reduce the risk of gout, but drinking coffee may not be appropriate for other medical conditions.
- Avoid foods such as white bread, cakes, candy, sugar-sweetened beverages and products with high-fructose corn syrup.
- Avoid organ and glandular meats such as liver, kidney and sweetbreads, which have high purine levels.
- Avoid the following types of seafood, which are higher in purines than others: anchovies, herring, sardines, mussels, scallops, trout, haddock, mackerel and tuna.
- Limit use of alcohol - no more than 2 drinks per day for a male or one drink per day for a female. The breakdown of alcohol in the body is thought to increase uric acid production. In addition, alcohol contributes to dehydration. Beer in particular is associated with an increased risk of recurring attacks of gout, distilled liquors to some extent as well.. The effect of wine is not as well understood, so moderation is recommended. (4)
- Avoid all alcoholic beverages if gout attacks are frequent or if gout is not well controlled.
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSC, BSP
medSask, July 2016
1) UpToDate - Becker MA, Clinical manifestations and diagnosis of gout. Romain PL, (Ed), UpToDate, Waltham, MA, 2015. Available at www.uptodate.com (by subscription). Accessed June 2016.
3) UpToDate - Becker MA, Prevention of recurrent gout .In:UpToDate. Romain PL, (Ed), UpToDate, Waltham, MA, 2015. Available at www.uptodate.com (by subscription). Accessed June 2016
1. Legality of taking drugs into other countries
Drugs that are prescriptions in Canada may be considered illegal or suspicious in some countries. International travellers should contact the foreign government offices accredited to Canada to make sure their medical supplies are allowed into the country. This contact information is available at: http://www.international.gc.ca/protocol-protocole/reps.aspx?lang=eng on the Government of Canada website.
2. Tips for air travel
All medications and associated supplies are allowed through airport security in the U.S. and Canada once they have been screened. However, some suggestions to help things go more smoothly include:
- Pack all medications in your carry-on baggage in their original, labelled containers. Prescription medication is exempted from the liquid restrictions but must be shown to the screening officer outside of your carry-on baggage. Do not pack essential medications in checked bags because of the risk for loss, theft, exposure to extreme temperatures, etc.
- Pack an extra supply of medication in case you are away for longer than expected.
- Keep a current list of prescriptions (ensure that both the generic and trade names of the medication are included) and medical conditions or a letter from your doctor, also in your carry-on bag. Include the names and phone numbers of your health care providers and pharmacies in case they have to be contacted.
- If possible, get an extra written prescription for a small supply of your medications, in case yours get lost. To be extra cautious, keep prescription medications in their original prescription containers, labeled with the same name as on your passenger ticket. (This is not required, but recommended.) Putting a reasonable quantity of pills in pill organizers is probably okay, but keeping medications in labeled containers may help avoid delays and problems.
- If in doubt that an item can be included in your carry-on and it is not needed for the duration of the flight, place it in your checked bag to avoid hassle. (Again, some experts caution against placing essential medications in checked bags because of the risk for loss, theft, exposure to extreme temperatures, etc., so use your judgement when packing)
- If a liquid medication is packed in your checked bag, seal the medication in a plastic bag to prevent leakage onto clothing and other luggage contents. If the bottle is glass, wrap it in cushioning material before sealing it in a plastic bag.
- The limit of two carry-on bags does not apply to medical supplies, equipment and mobility aids.
- Use the Family/Special Needs security line. Screening officers at these lines are trained to offer additional assistance.
- Do not buy medication outside Canada unless you have been advised to do so by a health care professional. Be aware of counterfeit medications or those that may not meet Canadian standards.
- Consult the Health Canada guide what you can bring on a plane to determine what you can and cannot pack in your carry-on luggage.
3. Diabetes supplies
Transportation Security Administration (TSA) recommends that patients with diabetes tell the screener that they have diabetes and that they are carrying diabetic supplies. Patients with insulin pumps may request a full-body pat down and visual inspection of their insulin pumps as an alternative to walking through the metal detector. It is safe to pass diabetes supplies through X-ray screening, but a visual inspection can be requested instead.
The following diabetes-related supplies and equipment are allowed through security checkpoints once they have been screened:
- Insulin and insulin-loaded dispensing products such as pens (must be clearly identified).
- Unlimited number of unused syringes (when accompanied by insulin or other injectable medication). If your medication requires needles and syringes, carry an explanation from your health care provider or a medical certificate with you. In some countries, a traveller found with needles and syringes and without an adequate explanation could be in serious trouble. Needles and syringes may be difficult to purchase abroad, so take enough to last your entire trip. Check airline regulations and the Canadian Air Transport Security Authority website before you travel to allow enough time to get the proper documentation as regulations differ from country to country.
- Lancets, blood glucose meters, blood glucose meter strips, alcohol swabs, meter-testing solutions
- Insulin pump and insulin pump supplies (must be accompanied by insulin)
- Glucagon emergency kit
- Urine ketone test strips
- Unlimited number of used syringes when transported in sharps disposal container or other similar hard-surface container
- Sharps disposal containers or similar hard-surface disposal container for storing used syringes and test strips.
4. Bringing medication back to Canada
To avoid interrupting a course of treatment, Health Canada may permit you to return from abroad with a single course of treatment or a 90-day supply, whichever is less based on the directions for use, of a prescription drug. The same regulations apply to bringing over-the-counter (OTC or non-prescription) medication back to Canada. The drug must be for your use or for the use of a person who is travelling with you and for whom you are responsible. The drug must be in hospital or pharmacy-dispensed packaging, the original retail packaging, or have the original label attached to it clearly indicating what the health product is and what it contains.
5. Travelling with a medical device, pacemaker or ostomy
Check with your doctor before flying to make sure it is safe for you to go through the metal detector at the security checkpoint. Always carry documents that support your medical condition. If you have a pacemaker, insulin pump or other medical device, you should advise the screening officer when you enter the screening area.
Before the screening process begins, inform the screening officer if you have an ostomy, and present him/her with a doctor's note. Although not mandatory, such supporting documentation will facilitate the screening process. If additional screening is required, a private search room is available.
More information on travelling with various medical devices can be found at:
6. Plan ahead
The limit of two carry-on bags does not apply to medical supplies, equipment and mobility aids. Make advance arrangements with your airline if you need to transport a battery-powered wheelchair or mobility aid or if you require someone to assist you through the pre-boarding screening are. Again, when you go through airport security screening, use the Family-Special Needs security line. Tell them if you have a medical implant, artificial limb or mobility aid that may trigger or be affected by the magnetic fields of the metal detection equipment.
7. Additional Resources
The CDC has tips for travelers with chronic illnesses at http://wwwnc.cdc.gov/travel/yellowbook/2012/chapter-8-advising-travelers-with-specific-needs/travelers-with-chronic-illnesses.htm
Since the regulations concerning medications and air travel are continuously being revised, use the following links to verify the most current regulations:
- United States:
- Transportation Security Administration (TSA) at http://www.tsa.gov/travelers/airtravel/specialneeds/disability-update.shtm;
- For a table of permitted and prohibited items, see http://www.tsa.gov/travelers/airtravel/prohibited/permitted-prohibited-items.shtm;
- For general information concerning travel security measures, see http://www.tsa.gov/travelers/index.shtm.
- Canadian Air Transport Security Authority/Administration (CATSA) canadienne de la surete du transport aerien at http://www.catsa.gc.ca/home.aspx?id=1&pname=Home_Accueil&lang=en.
Prepared by Jean Macpherson, BSP. Reviewed by Karen Jensen MSc, BSP
June 2016, medSask
- Travelling with medication. Government of Canada website. Available at https://travel.gc.ca/travelling/health-safety/medication. Accessed June 2016.
- PL Detail-Document, Have Meds Will Travel. Pharmacist’s Letter/Prescriber’s Letter. August 2012.
- Travelling with a medical device. Government of Canada website. Available at https://travel.gc.ca/travelling/health-safety/medical-device. Accessed June 2016.
Common warts are caused by a virus and are spread by direct skin-to-skin contact. They are small, raised growths which may be a different colour than the surrounding skin. They may contain black dots which are small, clotted blood vessels.
Warts around the fingernails are called periungual warts. Plantar warts are on the soles of the feet and flat warts are usually on the hands, face and lower legs.
Children, young adults and people with weakened immune systems are more likely to develop warts. They are also more common among certain occupations such as handlers of meat, poultry, and fish. You can also get infected by touching surfaces that have the wart virus on them, which is why they often occur in people who go barefoot around pools, locker rooms, or gyms.
Warts usually go away on their own, but may take a year or more to disappear and may reoccur. Many people want to remove them because they find them bothersome or embarrassing. (1, 2, 3)
The treatment for common warts depends on the location of the wart and patient preference. First-line treatments are:
- over-the-counter salicylic acid formulation applied on the wart at home
- cryotherapy (often called “freezing”) with liquid nitrogen in a doctor’s office or at home
More recently, the use of duct tape or adhesive tape as a treatment has gained popularity. (2, 4)
Salicylic acid (SA) applied to a wart works by slowly peeling away virus-infected skin. It may also help stimulate the immune system to react to the mild irritation, which in turn helps clear the infection. Effective treatment may take weeks or even months.
Various salicylic acid products are available without prescription in different strengths ranging from 17% to 40% and different formulations (solution, cream, gel, plasters and patches). These products are convenient to use, usually inexpensive, and do not cause pain if applied properly. They are most useful for plantar warts and sensitive body parts where cryotherapy would be painful. Plantar warts should be treated with the higher strength salicylic acid (up to 40%).
Package instructions should be followed exactly for the treatment to work. Before applying the SA product, the warts should be soaked in warm water for five minutes and then an emery board or pumice stone should be used to scuff and remove any dead skin. To avoid spreading the virus, it is suggested that a disposable emery board be used and thrown away after each use. The SA preparation should then be applied on the wart for the recommended time (as per package instructions). SA in liquid form should be applied every day and SA patches reapplied every 48 hours for up to 12 weeks. If the warts are not cleared after the recommended treatment time then a doctor should be consulted. (4)
Cryotherapy can be used instead of salicylic acid or if salicylic acid isn’t effective. It appears to work by causing irritation and tissue destruction which stimulates an immune response against the wart virus. One disadvantage of cryotherapy is the pain it often causes and because of this, it is used mostly to treat warts in older children and adults and often avoided in young children.
Liquid nitrogen, which freezes tissues to -196°C, is the most common agent used by doctors for cryotherapy. The treatment may take multiple visits to the clinic. Home use cryotherapy systems consisting of dimethyl ether and propane (DMEP) are also available. These agents freeze tissue to only
-57°C and do not freeze as quickly as liquid nitrogen. They appear to be almost as effective as treatments done in doctors’ offices, if applied properly.
After application of these products, a blister forms under the wart. The frozen skin and wart should fall off after about ten days. Contact with the blister fluid should be avoided as it may result in spreading the wart. OTC cryotherapy should only be repeated three times, usually at ten day intervals. (2, 4)
There is conflicting evidence as to whether or not duct tape treats warts effectively. Although the mechanism by which it works is unclear, it is suggested that covering the wart deprives the virus of oxygen and that the adhesive causes irritation, which stimulates an immune response to the virus, much the same as SA and cryotherapy.
Silver duct tape appears to work best because of the type of rubber-based adhesive on the tape. It is applied directly to the wart and removed six days later. The skin should then be soaked in warm water for 10 to 20 minutes, scrubbed with an emery board or pumice stone and left open to the air overnight. The cycle is repeated the next morning and every following six days for up to two months. One study showed that warts completely resolved in 85% of patients treated with duct tape and 60% of patients treated with cryotherapy. (2, 4)
A few alternative treatments have been reported to work for some people, but there is no reliable evidence to show they are as or more effective than salicylic acid and cryotherapy.
- Zinc – available as an ointment you apply to the wart or as an oral pill taken by mouth. The oral, pill form may be effective in people who have a zinc deficiency.
- Silver nitrate – available as a solution or ointment to be applied to the wart.
- Smoke – Some people showed benefit from treating their wart in a "smoke box" with smoke from burnt leaves of a type of poplar tree called Populus euphratica.
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
medSask, June 2016
- Mayo Clinic Staff. Diseases and Conditions. Common warts. In Mayo clinic online. Available at http://www.mayoclinic.org/diseases-conditions/common-warts. Accessed May 2016.
- Goldstein B, Goldstein A, Morris-Jones, R. Cutaneous warts. In UpToDate online database. Available at www.uptodate.com (with subscription). Literature review current through: Apr 2016. This topic last updated: Nov 10, 2015. Accessed May 2016.
- Dynamed. Verruca vulgaris. Available online at https://dynamed.ebscohost.com/ (by subscription). Accessed 09Jan2015.
- Treatment of cutaneous warts. Pharmacist's Letter/Prescriber's Letter 2010;26(7):260717.
Most medications remain active and safe to use for many years depending on how they are stored, BUT any medication taken after its expiry date is done so at the consumer’s risk. The manufacturer will not take responsibility for the effect or safety of a drug used after its expiry date.
The expiry date is important information for certain medications in order to be sure they will be effective. Talk to your pharmacist before using an expired product.
Background: An official definition of the manufacturer’s expiration date is the “date after which ideally stored medications in the unopened manufacturer’s storage container or in most circumstances, the opened and intact manufacturer’s storage container, should not be used. Manufacturers will usually set an expiry date of 2 to 3 years from the day the drug is made. The drug manufacturer must have evidence that until that expiry date, the drug is active at the strength stated on the label and is safe for use. This avoids the need for the manufacturer to do longer term testing for stability and may help make up for variability in storage conditions after a product is purchased and opened. (1, 2)
There are certain medications and dosage forms that should be replaced by or used before their expiration dates. Some drugs have shorter expiry dates because they break down more easily and are more sensitive to storage conditions. Examples are: epinephrine, nitroglycerin, insulin, antibiotics in liquid form, and eye drops.
Epinephrine used for allergic reactions (Allerject, Epipen) loses a significant amount of strength for each month past the expiry date, therefore epinephrine products should always be replaced before they expire. However, if there is a situation where epinephrine is needed and the only product available is outdated, it can be used as long as there is no discoloration or particles in the liquid. The benefit of using the outdated product is greater than the risk of a lower dose or of no epinephrine treatment at all. Follow-up as soon as possible at a hospital is required for anyone with an anaphylactic reaction, even if treatment is successful. A second occurrence of the allergic reaction happens in a high percentage of cases within 8 hours of the first episode.(3)
Drugs with a narrow therapeutic index should not be used after their expiry dates. A narrow therapeutic index means that a drug’s blood level needs to be within a precise range to be effective while at the same time avoiding adverse effects. Examples of such drugs are: carbamazepine (Tegretol), phenytoin (Dilantin), phenobarbital, digoxin (Lanoxin or Toloxin), theophylline (Theolair or Uniphyl) and warfarin (Coumadin).
Even if an expired drug is still within guidelines for strength after the expiry date, it may not be appropriate to use if there have been any changes in the health condition for which it was first prescribed. (1) Check with your pharmacist or doctor.
Prepared by Jean Macpherson, BSP. Rreviewed by Karen Jensen MSc, BSP
medSask, May 2016
1) Canadian Pharmacist’s Letter - PL Technician Tutorial, Drug Expiration Dates. Pharmacist’s Letter/Pharmacy Technician’s Letter. March 2015.
2) Expired Medications May Maintain Potency for Decades. Medscape. Oct 08, 2012.
3)Estelle F, Simone R, et al. Outdated EpiPen and EpiPen Jr autoinjectors: Past their prime? J Allergy Clin Immunol 2000; 105(5): 1025-1030
Halotherapy has been promoted in the media as a drug-free treatment for respiratory conditions such as chronic sinusitis, asthma, cystic fibrosis, and chronic obstructive pulmonary disease (COPD), as well as skin conditions such as eczema and other kinds of rashes.
Halotherapy (derived from the Greek word “halos” for salt) involves breathing in tiny salt particles while relaxing in special rooms or chambers that artificially mimic the climate of natural salt caves. The microclimate in the caves provides stable air temperature, moderate to high humidity, the presence of fine aerosol particles of various minerals and no or limited airborne pollution and pollens. This treatment has been more commonly used in spas in central and Eastern Europe and around the Dead Sea in Israel, but is becoming more available in North America. (1, 2)
The theory is that inhaled dry salt particles may loosen or liquefy airway mucous, which, in turn makes it easier to cough up and spit out secretions, helping to ease breathing. However, reviews of scientific literature reveal that very few studies have been done on halotherapy so there is little evidence to support its benefit. In one small study (2), twenty-nine patients were randomly assigned to either halotherapy or placebo inhalation five times a week for two weeks. The patients were then tested using an inhalation of histamine, which causes the airways to narrow. There was a slight improvement in response in the halotherapy group. In contrast, another trial did not find any difference in lung function and the need for a bronchodilator medication between patients in either group. (1)
Before halotherapy can be recommended, more high quality research is needed to determine whether or not it actually improves the quality of life of people with respiratory and other conditions. (3) There is also a lack of reliable evidence about the safety of halotherapy; however, at this time no safety issues are anticipated. (3)
Prepared by Jean Macpherson, BSP; reviewed by Karen Jensen MSc, BSP.
medSask, April 2016
- Martin RJ. Complementary, alternative, and integrative therapies for asthma. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed March 2016.
- Rashleigh R, Smith SMS, Roberts NJ. A review of halotherapy for chronic obstructive pulmonary disease. Int J Chron Obstruct Pulmon Dis. 2014; 9: 239–246. Published online 2014 Feb 21. doi: 10.2147/COPD.S57511 PMCID: PMC3937102. Accessed March 2016.
- Halotherapy. In: Natural Medicines Comprehensive Database. Stockton, CA: Therapeutic Research Faculty. [Monograph was last reviewed on 05/05/2015 and last updated on 08/11/2015; Accessed March 2016]. Available with subscription at http://naturaldatabase.therapeuticresearch.com.
Medical attention and antibiotic treatment are only needed if :
1. Infection with Lyme Disease is suspected:
- the attached tick has been identified as a “deer” tick AND
- the tick has been attached for ≥ 36 hours AND
- there is a high rate of Lyme disease infection in the local tick population. (That is not the case in Saskatchewan)
2. Lyme disease symptoms appear.
Most ticks found in Saskatchewan are “wood or dog” ticks and are found in long grass. The ticks that can carry Lyme disease are “deer” ticks and are found in wooded areas. Most deer ticks seen here have been carried in by migrating birds. Only a very small percentage of deer ticks (< 1%) carry the bacteria that can cause Lyme disease. There have been occasional sporadic cases of Lyme disease reported in Saskatchewan but most of these are related to travel to areas where Lyme disease is more common, such as British Columbia, Ontario, and parts of the U.S.
To identify the tick:
- Remove attached tick as soon as you find it.
- Using fine-nosed tweezers, grab the head and mouth as close to the skin as possible.
- Pull up slowly with steady pressure until the tick is completely removed from the skin.
- Do not twist or jerk the tick.
- Make sure the whole tick is removed.
- Wash the area with soap and water or disinfect with alcohol or household antiseptic.
- Avoid using nail polish, petroleum jelly, or heat to make the tick detach from the skin.
- Ticks may be saved in an empty pill vial (or similar) and sent in for testing (https://www.saskatchewan.ca/live/health-and...topics.../lyme-disease) or taken to the physician if symptoms develop.
- To tell the difference between the wood tick and the deer tick see:
To determine length of attachment:
- estimate time from possible exposure (when last in a wooded area?)
- how engorged was the tick? Even if a tick is attached, it must have taken a blood meal to transmit Lyme disease. At least 36 to 48 hours of feeding is required for a tick to have fed and then transmit the bacterium that causes Lyme disease. After this amount of time, the tick will be engorged (full of blood). An engorged tick has a globular shape and is larger than an unengorged one. See link above for pictures.
Lyme disease symptoms:
It is important to note that some people with Lyme disease may have no or minimal symptoms. Others may suffer severe symptoms. As well, some people may not develop symptoms until weeks after the initial bite.
- A typical sign of early Lyme disease is an expanding skin rash. It can occur at the site of the infected tick bite, usually in 7 to 14 days. The rash can appear as early as 3 days or as late as 30 days. It can persist up to 8 weeks. The rash is not usually painful or itchy, but it may be warm to the touch. About 50% of the rashes have a bull's eye appearance but may also be:
- solid orange to red color
- blue-purple in color
- Joint aches and pains
- Wear clothing that covers as much of your skin as possible and wear light coloured clothing to make the ticks easier to spot.
- Tuck pants into socks and wear shirts that fit tightly around your wrists.
- Use an insect repellent with DEET.
- Avoid the long grass-stay in centre of hiking trails.
- Keep your pets out of the wooded areas and long grass.
- Check yourself, your children, and your pets for ticks before coming indoors.
- On return from a tick-infested area, remove your clothes, shower, and check well for ticks.
- Wash and dry all clothes on the hottest setting to kill any remaining ticks.
Prepared by Dorothy Sanderson BSP; reviewed by Karen Jensen MSc, BSP
medSask, posted May 2015, updated May 2016
- Tick Fact Sheet - How to keep your family safe - SunCountry Health Region. Available at http://www.suncountry.sk.ca/service/212/88/tick-fact-sheet-how-to-keep-your-family-safe.html . Accessed May 2015.
- Government of Canada - Information for health professionals on Lyme disease. Available at http://www.healthycanadians.gc.ca/diseases-conditions-maladies-affections/disease-maladie/lyme/professionals-professionnels/index-eng.php . Accessed May 2015.
- Government of Saskatchewan - Lyme Disease
- Onyett H. Lyme disease in Canada: Focus on children. Canadian Paediatric Society , Infectious Diseases and Immunization Committee. Paediatr Child Health 2014;19(7):379-83. Available at http://www.cps.ca/en/documents/position/lyme-disease-children . Accessed May 2015.
- PL Detail-Document, Stepwise Approach to Lyme Disease: From Tick Bite to Treatment. Pharmacist’s Letter/Prescriber’s Letter. July 2014.
- Hu L. Evaluation of a tick bite for possible Lyme disease. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed May 2015.
Many people experience leg cramps at night while asleep and sometimes even while resting and awake. Nighttime or nocturnal leg cramps are usually harmless and are often related to muscle or nerve tiredness. (1) The cramps are caused by uncontrolled spasms of the muscle in the calf (back of the leg), the foot or the thigh. They occur suddenly, are painful and disturb sleep. (2, 3)
While leg cramps can affect anyone, they occur more frequently in older people (up to 50 % of seniors report episodes and pregnant women ( up to 50 % experience muscle cramps during the second half of pregnancy). (2, 4)
The actual cause is unknown, but cramps are sometimes set off by a movement such as pointing the toe down while lying in bed. This shortens the calf muscle, leading to cramping of the muscle. Vigorous activity or unaccustomed use of muscles at an earlier time in the day is sometimes followed by nighttime leg cramps. (5) Although as yet unexplained, cramps happen more often in mid-summer and less often in mid-winter. (6) Sitting for long periods, inappropriate leg position during sitting, and standing for long periods of time on concrete floors is associated with a higher incidence of leg cramps. (2)
Prevention / Treatment
Women who have leg cramps during pregnancy should discuss preventive measures and proper diet with their doctor to ensure they are getting all the required nutrients.
For other people, these types of cramps can sometimes be prevented by regular stretching of the affected muscles. Calf muscles can be stretched by standing about 2 ½ feet from a wall and by leaning into the wall while keeping back and legs straight with heels on the floor. This position should be held for 10 to 15 seconds and repeated two or three times a day and again before bed. Alternatively, when lying down, flexing or pulling the toes toward your head while keeping your legs as straight as possible will help stretch the calf muscles.
Stretching, as above, is often the best treatment when a cramp occurs. You can also try:
- walking or jiggling the affected leg followed by elevating it in bed with a pillow
- taking a hot shower or bath
- massaging and icing the muscle. (5)
Other strategies which may help to stop nocturnal cramps include:
- wearing proper, comfortable shoes
- keeping the bed covers at the foot of the bed loose and not tucked in
- drinking adequate fluids throughout the day to avoid dehydration
- making sure you are getting the recommended daily amount of calcium and Vitamin D (see Table 1 and 2 below). (2, 5)
If the above measures don’t work and nighttime cramping becomes frequent and is not sufficiently helped by stretching and massage, you should see your doctor to rule out other causes and to discuss other safe medical or prescription preventions and treatments.
Table 1: The Daily Reference Intakes for calcium8
Recommended Dietary Allowance (RDA) per day
Tolerable Upper Intake Level (UL) per day
Infants 0-6 months
Infants 7-12 months
Children 1-3 years
Children 4-8 years
Children 9-18 years
Adults 19-50 years
Adults 51-70 years
Adults > 70 years
Pregnancy & Lactation
- There is no additional health benefit associated with calcium intakes above the level of the new RDA.
- Total calcium intake should remain below the level of the new UL to avoid possible adverse effects.
- Long-term intakes above the UL (Upper Level) increase the risk of adverse health effects, such as kidney stone
- Consider total calcium intake from both dietary and supplemental sources. To figure out dietary calcium, count 300 mg/day from non-dairy foods plus 300 mg/cup of milk or fortified orange juice.
Table 2: The Daily Reference Intakes for vitamin D8
Recommended Dietary Allowance (RDA) per day
Tolerable Upper Intake Level (UL) per day
Infants 0-6 months
400 IU (10 mcg)
1000 IU (25 mcg)
Infants 7-12 months
400 IU (10 mcg)
1500 IU (38 mcg)
Children 1-3 years
600 IU (15 mcg)
2500 IU (63 mcg)
Children 4-8 years
600 IU (15 mcg)
3000 IU (75 mcg)
Children and Adults
600 IU (15 mcg)
4000 IU (100 mcg)
Adults > 70 years
800 IU (20 mcg)
4000 IU (100 mcg)
Pregnancy & Lactation
600 IU (15 mcg)
4000 IU (100 mcg)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
medSask, April 2016
1) Mayo clinic staff. Night leg cramps. In Mayo Clinic online. Available at http://www.mayoclinic.org/symptoms/night-leg-cramps/basics/definition/sym-20050813. Accessed 11Sep2015.
2) Winkelman JW. Nocturnal leg cramps. In: UpToDate, Romain, PL (Ed), UpToDate, Waltham, MA, 2015. Available at www.uptodate.com (by subscription). Accessed 11Sep2015.
3) Nocturnal Leg Cramps. In Dynamed online database. Available at https://dynamed.ebscohost.com/ (by subscription). Accessed 11Sep2015.
4) CPL: How to prevent nighttime leg cramps. Pharmacist's Letter/Prescriber's Letter 2010;26(6):260606.
5) Muscle Cramps. In Medicinenet.com. Available at http://www.medicinenet.com/muscle_cramps/article.htm. Accessed 11Sep2015.
6) Garrison S, et al. Seasonal effects on the occurrence of nocturnal leg cramps: a prospective cohort study. CMAJ. 2015 Mar 3;187(4):248-53. doi: 10.1503/cmaj.140497. Epub 2015 Jan.
7) Calcium and vitamin D supplementation: who needs it? Pharmacist's Letter/Prescriber's Letter 2011;27(1):270102.
8) What are the new DRIs for Calcium? Health Canada. Available at http://www.hc-sc.gc.ca/fn-an/nutrition/vitamin/vita-d-eng.php#a7. Accessed 11Sep2015.
The use of saline nasal sprays and rinses (known as nasal irrigation) is routinely recommended for relieving symptoms of colds, allergies and sinus congestion. Familiar product names are hydraSenseÒ, Otrivin SalineÒ, NeilMed Sinus RinseÒ, Neti Pot and others. These products are easy to use and can be purchased without a prescription, but is there any evidence that they are useful for treating these conditions?
A review of studies showed that the length of time required to recover from a cold was not shortened by the use of nasal irrigation, but that there may be relief of some symptoms, such as runny nose and mucous thickness. (1, 2)
Allergy (hay fever):
A study of the usefulness of saline rinses in children with inflamed sinuses from allergies, showed that nasal irrigation significantly improved runny nose, nasal congestion, throat itching, sleep quality symptoms, and nasal air flow. Another study found that the beneficial effects of nasal irrigation were greater when used with steroid nasal sprays such as fluticasone (FlonaseÒ) and mometasone (NasonexÒ), or others.
Nasal irrigation is particularly helpful when there are crusted nasal secretions due to chronic, thick drainage. The nasal passages can be cleansed with saline before using the steroid sprays to help increase the amount of medication that actually reaches the lining of the nose.
A study of pregnant women found saline irrigation helped to improve nasal symptoms of allergy. This is particularly helpful for women who want to avoid unnecessary medications while pregnant. (3)
Chronic sinusitis is defined as an inflammation of the sinuses and linings of the nasal passages, which lasts for 12 weeks or longer.
At least 2 of the following 4 symptoms must be present for the diagnosis of chronic sinusitus:
●Pre and/or post-nasal drainage of mucous (runny nose or post-nasal drip)
●Nasal obstruction (plugged nose)
●Facial pain, pressure, and/or fullness
●Decreased sense of smell (4)
Nasal saline irrigation can be useful for allergic and chronic rhinosinusitis, improving symptoms by about 30%. (1) Chronic sinusitis cannot be "cured" in most patients, so therapy is intended to reduce symptoms and improve quality of life.
Washing the nasal cavities with saline reduces postnasal drainage, removes secretions, and rinses away allergens and irritants. Saline washes can be used immediately before other intranasal medications so that the lining of the nose is freshly cleansed when the medications are introduced. (4, 5)
Directions for use
There are a number of devices available, including squeeze bottles, sprays, bulb syringes and Neti pot containers and all are effective provided the system delivers enough of the solution (>200 mL per side) into the nose. Nasal irrigation with warmed saline can be used as needed only, or once or twice daily for increased symptoms. It carries little risk if properly performed, with minor adverse effects, such as nasal burning and irritation.
Patients can make their own irrigation solutions or buy commercially-prepared solutions or kits.
To make a solution that is close to isotonic (0.9%) use one teaspoonful salt in three cups water (720 mL).
One-half teaspoonful of baking soda is often added to improve tolerability. It is important that the solutions be prepared from sterile or bottled water, as there have been reports of amebic encephalitis due to rinses with tap water that was contaminated. Although rare, it is usually fatal. Irrigation devices can also become contaminated with the bacteria present in the patient's nasal cavities, although it is not clear that this causes any significant problems. However these devices should be cleaned as directed after each use and replaced regularly (3, 5, 6)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen BSP, Msc
medSask, March 2016
1. Sexton, D and McClain, M. The common cold in adults: Treatment and prevention. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed March 2016.
2. Alberta College of Family Physicians - Tools for Practice #155. Authors: Emma Huang BScPharm, G Michael Allan MD CCFP. Available online at: https://www.acfp.ca/wp-content/uploads/tools-for-practice/1454016118_tfp155salinenasalrinsefv.pdf
3. deShazo, R and Kemp, R. Pharmacotherapy of allergic rhinitis. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed March 2016.
4. Hamilos, D. Chronic rhinosinusitis: Management. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed March 2016.
5. Saline nasal irrigation and use of neti pots. Pharmacist's Letter/Prescriber's Letter 2010;26(1):260105.
6. Patel, Z and Hwang, P.Uncomplicated acute sinusitis and rhinosinusitis in adults: Treatment. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed March 2016.
Yes, you will have to get a prescription from your doctor in order to obtain the vaccine.
Shingles is a painful, blistering rash caused by the same virus that causes chickenpox. The chickenpox virus (varicella-zoster) stays in your nerve cells after the chickenpox blisters heal. It may remain dormant for many years and not cause a problem, but in some people it may become reactivated for unknown reasons and cause shingles.
Shingles usually occurs in one part of the body, frequently around bottom of the rib cage. The rash can last for several weeks and may result in scarring. The nerve pain that comes from shingles can last for months or years after the rash heals. This is known as post-herpetic neuralgia.
The shingles vaccine, Zostavax™ II, is recommended for people over the age of 60 years to prevent shingles. The vaccine works by boosting your immune system to reduce your risk of getting shingles and the associated pain and other serious complications. It reduces the risk of getting shingles from 6.6% to 2.0%. If you do get shingles even though you have been vaccinated, the vaccine may reduce the pain and length of time the pain from shingles will last.
Many insurance plans do not cover the cost of Zostavax™ II, it is not on the Saskatchewan Drug Plan Formulary, and is not included in the publicly funded immunization programs. The cost to the patient is about $220 (as of January 2016). If you have an insurance plan that does cover this vaccine, you will require a prescription receipt for reimbursement. Check with your insurance plan to ensure it will cover this vaccination and what documentation is required for reimbursement.>
Because the vaccine must be stored in the fridge at 2-8°C or colder before it is ready for injection, not all clinics, physicians’ offices or pharmacies will have Zostavax™ II in stock. Talk to your pharmacy, as in most cases it can be ordered and delivered the next day.
Prepared by Jean Macpherson BSP/Dan Johnson BSc. Reviewed by Karen Jensen MSc, BSP and Carmen Bell BSP.
- Health Canada Drug Product Database – product monograph for Zostavax available at http://www.hc-sc.gc.ca/dhp-mps/prodpharma/databasdon/index-eng.php
- National Advisory Committee on Immunization (NACI). Update on the Use of Herpes Zoster Vaccine. January, 2014.
- Albrecht, Mary A. Prevention of varicella-zoster virus infection: Herpes zoster. In UpToDate, Hirsch,MS(Ed), UpToDate, Waltham, MA, 2015
- Saskatchewan Prescription Drug Plan. http://formulary.drugplan.health.gov.sk.ca/
- McKesson Canada; c2016 [cited 2016 Mar 7] PharmaClik; Available from http://clients.mckesson.ca.
None of the detox and cleanse methods have any reliable evidence of effectiveness in removing toxins or preventing diseases. Some can be dangerous depending on how they are used, how often they are used and whether they are being used in place of proven medical treatments.
New Year’s resolutions to lose weight and get healthy, may lead people to try “detoxes” or “cleanses”. Along with food and calorie restrictions, these may involve products which contain ingredients that claim to help the liver, the kidneys and the colon rid the body of accumulated wastes and chemicals. They are advertised as agents to help lose weight, boost energy and remove toxins. (1)
Promotors claim toxins don't always leave our bodies properly in the form of sweat, urine or feces, but instead hang around in the digestive, lymph, and gastrointestinal systems as well as in skin and hair. They suggest that this can cause problems such as inflammation and allergies. (2)
Cleanses taken by mouth are made up of herbs and dietary fiber. They have no proven benefit and can be expensive.
Liver cleanses usually contain milk thistle and other ingredients. Milk thistle alone at doses of up to 600mg/day appears to be safe, but may cause diarrhea, upset stomach and allergic reactions. (1, 3)
Colon (large intestine) cleanses usually contain fiber, laxatives and herbs and are sometimes used along with probiotics to restore healthy digestive system bacteria. While fiber and exercise will usually work for constipation, when taken in the doses used for cleansing they can lead to diarrhea, resulting in fluid loss and electrolyte (mineral) imbalances.
Rectal use of cleansing enemas or colonic irrigation often consists of pumping large amounts of liquids into the colon via a tube.
Rectally administered coffee enemas used for detoxification have been linked to at least three deaths. Two of these deaths were related to severe electrolyte imbalance, and a third was associated with infection. (1, 3, 4)
Healthy detox diets usually encourage eating organic foods with high nutrient and high fiber content. Elimination of foods containing “toxins” such as alcohol, caffeine, processed sugar, certain grains, and some dairy foods and meats are proposed to help the body recover from over-indulgence.
Some detox regimens suggest avoiding solid foods (e.g. juice fasting) or eating higher quantities of single foods (e.g. grapefruit diet). These will sometimes combine the diet with herbal supplements or rectal enemas and can last for days to weeks. Some are safe in the short-term, but long-term fasting can result in nutrient and protein deficiencies. (1)
People who have certain medical conditions should not try any of these fads without first checking with their medical doctor, in particular:
ANEMIA: People with iron or vitamin deficiency anemia should avoid detoxification programs that restrict foods that provide these nutrients. Dietary restriction of these nutrients could worsen anemia.
CRITICAL ILLNESS: Patients with serious illness such as cancer should avoid detoxification programs that restrict eating adequate amounts of food or restrict certain groups of food. Diseases could worsen if necessary nutrients are restricted.
ENDOCRINE DISORDERS: People with diabetes, thyroid disorder, or other endocrine disorders should avoid detoxification programs that require dramatically changing food and calorie intake without appropriate medical supervision. Substantial dietary changes could potentially worsen these conditions or require changes in treatment. (3)
Prepared by Jean Macpherson BSP, reviewed by Karen Jensen BSP, MSc
medSask, January 2016
1) Colon and liver detoxification. Pharmacist's Letter/Prescriber's Letter 2010;26(2):260211.
2) What is a detox diet? Teen Health. Available at http://kidshealth.org/teen/food_fitness/dieting/detox_diets.html. Accessed January 2016.
3) Milk thistle In: Natural Medicines Comprehensive Database. Stockton, CA: Therapeutic Research Faculty. Available at www.naturaldatabase.com (by subscription).
4) Barrett S. Questionable cancer therapies. Quackwatch online. Available at http://www.quackwatch.org/01QuackeryRelatedTopics/cancer.html. Accessed January 2016.
Hair loss can be the result of heredity, hormonal changes, medical conditions or drugs. Whatever the cause, hair loss can be distressing. In some cases it can be slowed down or reversed, while other times appearance can be managed with cosmetic hair products.
Background: Of the 100,000 to 150,000 hair follicles on the head, most people will lose between 50 and 100 hairs a day. Hair breakage can also affect the appearance of fullness. Hair care practices that damage the hair shaft such as wearing tight braids, cornrows or ponytails for long periods can contribute to breakage and even to bald spots (alopecia). Chemical treatments such as perms, straighteners or bleaching can cause breakage and inflammation of hair follicles that can lead to hair loss. If scarring occurs, hair loss may be permanent.
The most common type of hair loss is androgenic alopecia (male and female pattern hair loss) caused by an excess in a hormone that destroys scalp hair follicles. In women, this may occur gradually with aging particularly after menopause.
When hair loss is the result of a medical condition or is stress-related, treating the condition may help to restore a healthy head of hair. Most women who experience hair loss after childbirth will gradually recover their normal hair thickness within about 15 months. Hair loss that is caused by a drug (examples below) may get better the longer the drug is taken or may reverse if the drug is stopped. When hair loss is due to some types of chemotherapy (cancer treatment), re-growth usually starts about two months after the drugs are stopped. If you think a medication you are taking might be causing hair loss, talk to your pharmacist or doctor about it.
Low levels of zinc, iron, biotin, lysine, or vitamin D or diets that are too low in calories or protein can also cause hair to thin. Nutritional supplements may help over time if a person has a deficiency.
Minoxidil 5% (RogaineÒ and generics) foam is the recommended non-prescription treatment for androgenic alopecia in both men and women. With this treatment, some people experience hair regrowth, a slower rate of hair loss or both. The effect might not be noticeable for 2 to 4 months and full results might not be seen for a year. An increase in the amount of hair that falls out may start within 2 to 6 weeks of beginning to use minoxidil. This is normal and should stop with continuous use. If hair loss continues for longer than 2 weeks, it is recommended to stop using the product.
The foam is massaged into the affected area of the scalp once a day and left on for at least 4 hours.
Minoxidil treatment must be ongoing to retain benefits. Possible side effects include scalp irritation, unwanted hair growth on the adjacent skin of the face and hands, and rapid heart rate (tachycardia).
Natural products: A small study found that a mixture of lavender, thyme, rosemary, cedarwood, jojoba and grapeseed oils, improved hair growth. The mixture was applied daily for 7 months. However, more studies are needed to confirm that this product is effective. There is not enough evidence to recommend other herbal compounds for restoring hair growth.
Low-level laser therapy (LLLT) for hair growth in both men and women seems to be safe and somewhat effective. The theory behind this is that laser light of certain wavelengths can stimulate hair follicles to re-enter and maintain the growth phase. There are few scientific studies that document the degree of effectiveness of lasers on hair growth, however there appears to be a low incidence of adverse effects, aside from a short-term increase in shedding at the beginning (first 1-2 months) of therapy. LLLT should not be used by anyone with melanoma or skin cancer as it could increase the growth of cancerous lesions. Equipment for at-home laser therapy can cost up to $1000 and treatment must be ongoing to maintain effectiveness.
Table 1: Drugs associated with hair loss in ≥ 5% of patients
ACE Inhibitors - class of drugs to lower blood pressure
Reported more often with ramipril
Warfarin – may affect >50% of people with high doses
Most likely with terbinafine (LamisilÒ) and fluconazole (DiflucanÒ and others)
Indinavir (CrixivanÒ) may affect up to 10% of people
Anastrozole (ArimidexÒ) and exemestane (AromasinÒ)
Timolol most likely – others rarely
Percentage varies depending on type of drug
Cholesterol Lowering Drugs
Lovastatin (MevacorÒ and others) most likely - others rarely
Cyclosporine (NeoralÒ), leflunomide (AravaÒ), mycophenolate (CellceptÒ),
Tacrolimus (PrografÒ) – up to 28%
IntronÒ, PegasysÒ and others
Carbamazepine (TegretolÒ and others), lithium (LithaneÒ and others), valproic acid (DepakeneÒ and others),
divalproex (EpivalÒ and others)
Acitretin (SoriataneÒ), isotretinoin (AccutaneÒ and others)
Novaldex-D and others
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen BSP, MSc
medSask, January 2016.
- Shapiro, J, Otberg, N, Hordinsky, M. Evaluation and diagnosis of hair loss. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed December 2015.
- Hair Care and Hair Growth. RxTx – Minor ailments. Available from: http://www.e-therapeutics.ca (by subscription). Date of Revision: November 2014. Accessed online December 2015.
- Pomeranz, M.The skin, hair, nails, and mucous membranes during pregnancy. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed December 2015.
- 4.. Mayo Clinic Staff. Diseases and Conditions. Hair loss. In Mayo Clinic online database. Available at http://www.mayoclinic.org/diseases-conditions/hair-loss/basics/definition/con-20027666. Accessed December 2015.
- Natural Product Effectiveness Checker. Natural Medicines Comprehensive Database. Available online by subscription. Accessed December 2015.
- Avci, P., Gupta, G. K., Clark, J., Wikonkal, N. and Hamblin, M. R. (2014), Low-level laser (light) therapy (LLLT) for treatment of hair loss. Lasers Surg. Med., 46: 144–151. doi: 10.1002/lsm.22170.
- Lúcio Frigo et al. The effect of low-level laser irradiation (In-Ga-Al-AsP - 660 nm) on melanoma in vitro and in vivo. BMC Cancer 2009; 9: 404. Published online 2009 Nov 20. doi: 10.1186/1471-2407-9-404.
- Canadian Pharmacist’s Letter - Drugs associated with hair loss. Pharmacist's Letter/Prescriber's Letter 2011;27(2):270215.
Q. When I fly I always experience very unpleasant ear pain and loss of hearing. What can I do?
Use of oral decongestants, antihistamines, and nasal decongestant sprays prior to flying or diving may reduce obstruction around the Eustachian tube and allow for easier pressure equalization. Pseudoephedrine tablets taken 30 minutes prior to flight may reduce the ear discomfort caused by changes in air pressure during take-off and landing. The nose spray decongestant oxymetazoline is somewhat less effective. These can be used together but we suggest trying pseudoephedrine first. If you still have ear pain, you can use the nose spray in combination with pseudoephedrine.
Other measures that might help include:
- Swallowing frequently or using the Valsalva maneuver (blowing into your nose while holding your nostrils closed and keeping your mouth shut to open the Eustachian tube or using the Valsalva maneuver (positive pressure against a closed nasal airway) helps to even out the pressure in your ear.. Doing this frequently during take-off and landing can prevent large pressure differences from forming and prevent any damage to your ears. Chewing gum or sucking on hard candies helps for adults, sucking on a bottle or nursing helps for infants.
- Ear plugs designed to slow down the pressure changes from flying are available in drug stores and most airports. These allow the pressure change to take place more gradually. Their benefit, however, has not been clearly demonstrated.
- Avoid sleeping during takeoff and landing.
There are numerous mental health services that are accessible through the Saskatoon Health Region:
- Mental Health and Addiction Services – Centralized Intake Line: 306-655-7777
- Visit the Saskatoon Health Region website for more information
- List of Mental Health and Addictions Services in Saskatoon
Needing immediate advice?
Mobile Crisis Line Saskatoon: 306-933-6200 (24-hour service)
Health Line: 811 (has Mental Health Worker or Psych Nurse available 24 hours)
Online self-help resources:
Mental Health Problems - Courses:
Needing to see a psychiatrist or psychologist?
That depends on what you are taking. Some medications should not be mixed with alcohol at all, while one or two alcohol drinks may be fine with others.
Medication and alcohol combinations which could be risky:
- Central nervous system drugs. If you take any drugs known to cause central nervous system (CNS) depression or slow down brain activity, alcohol should be avoided. These types of drugs are often called sedatives, tranquilizers, mood-stabilizers or sleeping pills and may be used to treat anxiety, insomnia and other conditions. Since ethanol (ethyl alcohol) can also cause a slowing of brain activity, this effect can be stronger when taken with other drugs that have the same effect.
- Opioid or narcotic pain medicines (e.g. codeine, morphine and others), are also CNS depressants and alcohol should be avoided while taking these. Blood alcohol levels, even within the legal driving limits, may be very unsafe in the presence of other CNS depressants.
- Combining sedatives or narcotics with alcohol is an increasingly common cause of overdose and death.
- Extended, slow or controlled release (e.g. those with XR, SR or CR in the name). These drugs might be a problem if alcohol alters the special formulation that allows the drug to be released slowly or affects the way the stomach absorbs the drug. This might result in “dose-dumping”, a higher than prescribed or dangerous amount of drug getting in to the bloodstream. Check with your pharmacist if you are unsure about the formulation of your particular medication.
- Antihistamines. These are drugs such as diphenhydramine (Benadryl), chlorpheniramine (Chlortripolon) and dimenhydrinate (Gravol) which often cause CNS side effects such as drowsiness. Alcohol should be avoided with these until you know how they affect you. Other “non-drowsy” antihistamines such as loratadine (eg, Claritin), cetirizine (eg, Reactine), deslopratadine (Aerius) and others may be a safer alternative with alcohol.
- Antidepressants. These are drugs such as amitriptyline (Elavil), nortriptyline and MAOIs (monoamine oxidase inhibitors) which can cause CNS depression side effects and should be used cautiously alcohol especially when the prescription is first started. MAOI’s (Parnate, Nardil) have dietary restrictions as well as alcohol restrictions, so avoidance is advised. Bupropion (Wellbutrin) can make a person more sensitive to alcohol intoxication as well as increase the risk of seizures when combined with alcohol. Other anti-depressants such as fluoxetine (ProzacÒ and other related SSRIs or SNRIs) appear to be safer with alcohol.
- Antidiabetic medicine: Acohol can affect blood sugar and when taken with anti-diabetes medications or insulin, the levels can become unpredictable, causing highs or lows. Alcohol taken with metformin can also cause lactic acidosis (a build-up of lactic acid in the blood). Use alcohol cautiously and with moderation if you have diabetes.
- Antibiotics: In most cases alcohol is OK with antibiotics. An exception would be the antibiotic metronidazole (Flagyl) which can cause a potentially serious reaction when alcohol is taken while using the drug and for up to 3 days after stopping the drug. Antifungal medications such as ketoconazole (Nizoral) can cause the same reaction.
- Acetaminophen (e.g. Tylenol): An occasional drink is usually OK but if you have 3 or more drinks a day you should avoid acetaminophen because the combination can damage your liver.
- Ibuprofen, naproxen (e.g. Advil, Aleve) and other NSAIDs (e.g. diclofenac, Celebrex, Toradol and others): These drugs can cause bleeding of the stomach lining. Alcohol, especially if you have three or more drinks daily, can worsen this problem because it also can cause bleeding in the digestive tract.
- Blood thinners: Drinking alcohol can increase the risk of falls and bleeding. Caution is advised when taking “blood thinners” and other drugs that affect clotting such as warfarin, dabigatran (Pradaxa), clopidogrel (Plavix) and others (e.g. Xarelto, Eliquis).
- Blood pressure medicines: An occasional drink is probably OK if you are on blood pressure medicines. Some can cause a temporary drop in blood pressure when you stand up from a lying or sitting position and alcohol could worsen this effect increasing the risk of falling. The effect of beta –blockers such as metoprolol can increase with alcohol causing temporary increases or decreases in blood pressure.
- Varenicline (Champix): Combining alcohol with the smoking-cessation drug varenicline (Champix) can increase drunkenness, willingness to fight and memory loss. Use alcohol with caution if you are on this medication and especially if you have side effects while on it.
- Canadian Pharmacist’s Letter -PL Detail-Document, Alcohol and Drug Interactions. Pharmacist’s Letter/Prescriber’s Letter. December 2015.
- Lexicomp Online Interactions available at http://www.e-therapeutics.ca/search#
- UpToDate. Prescription drug misuse: Epidemiology, prevention, identification, and management. Accessed December 2015.
There is no scientific evidence to support any cure or effective prevention for alcohol hangovers. The most effective way to avoid a hangover is to consume alcohol only in moderation or not at all.
Alcohol has many effects on the body that contribute to the hung-over feeling. Dehydration due to alcohol results in headaches, muscles pains, fatigue and irritability. Alcohol causes inflammation of the stomach lining and increases gastric acid production leading to abdominal pain, nausea and vomiting. It can also lower blood sugar and disrupt sleep cycles. These disruptions in body rhythms produce a “jet lag” effect.
If you are going to drink, try to limit the amount to one or fewer drinks per hour and alternate with a glass of water to reduce dehydration. Alcoholic beverages that contain few congeners (biologically active compounds that contribute to the taste, smell and appearance of the alcoholic beverage) such as vodka, gin and rum are associated with a lower incidence of hangover than are beverages that contain a number of congeners, such as brandy, whiskey, bourbon and red wine.
Food of any kind before indulging in alcohol helps to lessen hangover symptoms, but fatty foods in particular stick to the stomach lining longer and therefore slow down the absorption of alcohol into the blood stream. This gives the body more time to process the by-products of alcohol.
Treatment of hangover
- Drink lots of water to replenish fluids and dilute toxins. Hangover symptoms will usually abate over 8 to 24 hours. There is no evidence that sports drinks are more effective than water for a hangover.
- Caffeine is commonly used to counteract the fatigue and malaise associated with hangover condition, but can also contribute to the dehydration.
- Carbohydrates in the form of toast or crackers and fruit juices increase blood sugar and may help reduce fatigue and irritability.
- Eggs and high protein foods contain an amino acid known as cysteine which may help detoxify the harmful by-products of alcohol in the body.
- ASA and other anti-inflammatories, such as ibuprofen or naproxen, may reduce the headache and muscle aches, but should be used cautiously if upper abdominal pain or nausea is present. These are gastric irritants and will compound alcohol induced gastritis. Acetaminophen should be avoided during the hangover period because alcohol metabolism enhances acetaminophen toxicity to the liver.
- Do NOT drink more alcohol (“hair of the dog”). It may provide temporary relief but only prolongs the hangover process.
The following are signs and symptoms of alcohol poisoning that require emergency medical treatment:
- Confusion, dazed feeling
- Persistent vomiting
- Irregular or slow breathing (less than eight breaths a minute)
- Blue-tinged skin or pale skin
- Low body temperature (hypothermia)
Prepared by Jean Macpherson BSP, December 14, 2009.
Updated December 16, 2014.
1. Swift R, Davidson D. Alcohol hangover; mechanisms and mediators. Alcohol, Health and Research World 1998;22:54. Available at http://pubs.niaaa.nih.gov/publications/arh22-1/54-60.pdf. Accessed 14Dec2009
2. Perry L. How hangovers work. Available at http://health.howstuffworks.com/hangover5.htm. Accessed 14Dec2009.
3. Weise J, Shlipak M, Browner W. The alcohol hangover. Ann Intern Med 2000;132:897, Available at http://www.annals.org/content/132/11/897.full. Accessed 14Dec2009.
4. Mayo Clinic. Hangovers. Available at http://www.mayoclinic.org/diseases-conditions/hangovers/basics/symptoms/con-20025464. Accessed 15Dec2014
5. Pittler M, Verster JU, Ernst E. Interventions for preventing or treating alcohol hangover: systematic review of randomised controlled trials. BMJ 2005;331:1515. Available at http://www.bmj.com/content/331/7531/1515.full.pdf+html. Accessed 15Dec2014.
Mild cases of dandruff may need nothing more than daily cleansing with a gentle shampoo. Although a relatively stable condition, dandruff can worsen with poor hygiene or in a dry winter environment. More stubborn dandruff may require treatment with medicated shampoos or corticosteroid products.
Dandruff is the mildest form of a condition called seborrheic dermatitis (seborrhea). It generally affects just the scalp and does not cause inflammation. Seborrhea, in comparison, is an inflammatory skin condition which causes red patches and scaling of the scalp as well as other oily areas of the body such as the face, upper chest and back. It occurs in about three percent of the population, most commonly in infants up to three months of age (“cradle cap”) and in adults 30–50 years of age. It tends to affect men more than women. In some cases seborrhea is associated with a yeast-like fungus called Malassezia which may be present on the scalp and cause inflammation.
Dandruff symptoms are easy to spot: white, oily looking flakes of dead skin on your hair and shoulders, and possibly an itchy, scaly scalp. Although uncommon in childhood (especially in children younger than 10), dandruff usually begins between ages 10–20 years, and affects up to 40% of men and women over age 30. It isn't contagious and is rarely serious.
Recommended treatment of dandruff and mild seborrhea of the scalp for ages 12 years and over:
- Dandruff may improve in a moist environment so using a humidifier especially in winter may help.
- Initial treatment using a regular, non-medicated shampoo at least 3 times a week may be all that is needed to control symptoms and improve the appearance of the hair.
- If this is ineffective, the next step is to try an antifungal shampoo. The antifungal ingredients available without prescription are ketoconazole (e.g. Nizoral), selenium sulfide (e.g. Selsun Blue products and others) and zinc pyrithione (e.g. Head and Shoulders products and others).
- To be effective, the shampoo must be massaged into the scalp thoroughtly and left on for 3 to 5 minutes before rinsing. Once the dandruff is under control, which may take 2 to 4 weeks, use of the antifungal shampoo once a week may help to avoid a recurrence.
- If you have a lot of redness or itching, inflammation may be present. Ask your pharmacist or doctor if a corticosteroid cream such as 0.5 – 1% hydrocortisone (Cortate, etc.) or clobetasol butyrate (Spectro eczema cream) would be helpful. Either of these may be used once or twice daily for 1 to 3 weeks to reduce symptoms and then stopped once the symptoms are under control. This treatment can be repeated after a rest period if needed.
- If there is still no response, the next step to try would be products containing salicylic acid and/or sulfur. These have minimal antifungal activity but are sometimes effective because of their keratolytic (softening and peeling action) and antiseptic actions. Coal tar shampoo is mildly effective for seborrhea because it reduces local swelling and inflammation, relieves itching and is keratolytic and antiseptic. It has little antifungal activity. Coal tar is messy, can stain blond or grey hair and has an unpleasant odour. It is used once daily to once weekly. (1, 3)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
medSask, November 2015
- Dandruff and Seborrhea. RxTx – Minor ailments. Available from: http://www.e-therapeutics.ca (by subscription). Date of Revision: November 2014. Accessed online November 2015.
- Sasseville, D. Seborrheic dermatitis in adolescents and adults. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed November 2015.
- 3. Mayo Clinic Staff. Diseases and Conditions. Dandruff. In Mayo Clinic online database. Available at http://www.mayoclinic.org/diseases-conditions/dandruff/basics/definition/con-20023690, Accessed November 2015.
Cradle cap (yellowish, greasy scales on a baby’s scalp) will usually clear up on its own in a few months. It can be treated by washing the baby's scalp daily with a mild baby shampoo and loosening the scales with a small, soft-bristled brush before rinsing off the shampoo.
If the scales don't loosen easily, rub petroleum jelly or a few drops of mineral oil onto baby’s scalp. Let it soak into the scales for a few minutes, or hours if needed. Then brush and shampoo the hair as usual. If you leave oil in the hair, the cradle cap may get worse.
Once the scales are gone, wash your baby's hair every few days with a mild baby shampoo to prevent scale buildup.
- Dandruff and Seborrhea. RxTx – Minor ailments. Available from: http://www.e-therapeutics.ca (by subscription). Date of Revision: November 2014. Accessed online November 2015.
- Sasseville, D. Cradle cap and seborrheic dermatitis in infants. In UpToDate online database. Available at www.uptodate.com (with subscription). Accessed November 2015.
Cetaphil Gentle Cleanser has been shown to be effective in a few small studies. (1-3) The first-line treatment recommended for head lice is still 1% permethrin (Nix, etc.) or pyrethrins (R&C, etc.).(4) These products should be reapplied in 7 to 10 days even if labels say otherwise. Other non-prescription products such as Resultz (isopropyl myristate) or Nyda (dimeticone) are available in Canada if the first-line options are not effective (4). Some evidence suggests they work as well as permethrin; however, since they are newer there is less evidence for effectiveness and safety. Nit combing after a treatment is always recommended regardless of which product is used because none are 100% effective at killing the eggs (4).
Cetaphil Gentle Cleanser is an alternative that can be tried if other treatments have failed or if people want to avoid insecticides. When used, the hair should be carefully inspected for new lice for a few weeks to ensure the product was effective. It is suggested that treatments be repeated for at least three weekly cycles (5).
Cetaphil Gentle Cleanser works by coating the lice and plugging their breathing openings so that they suffocate. It must be used exactly as recommended (see below) in order to be effective (5). Products like Cetaphil that suffocate live lice are not very effective in killing the eggs, so the lice problem returns as soon as the nits hatch, requiring additional applications of the product.
In clinical studies, Cetaphil Gentle Cleanser was applied to the scalp, the hair combed to spread the product along each hair shaft, then blow-dried to coat the lice in a shrink-wrap-like layer. The dry lotion was left on the hair and scalp for a minimum of eight hours. This procedure was repeated twice at one week intervals for a total of three applications (1-3).
Lice and their nymphs can survive for up to three days away from humans, as can their eggs, although the eggs require scalp temperature to hatch. Extensive housecleaning is not necessary if a family member has lice. They are spread by head to head contact. They can move quickly, but do not jump or fly. Items that have been in contact with the hair should be washed in hot water (66oC) and dried in a hot dryer for 15 minutes, or stored in a plastic bag for two weeks. There is no medical reason for keeping children with lice home from school because by the time lice are spotted, the child has been infected for over a month (4).
1) Perlman D. A Simple Treatment for Head Lice: Dry-On, Suffocation-Based Pediculicide. Pediatrics 2004;114(3) e275.
2) Barker S, Altman P. A randomized, assessor blind, parallel group comparative efficacy trial of three products for the treatment if head lice in children – melaleuca oil and lavender oil, pyrethrings and piperonyl butoxide, and a “suffocation” product. BMC Dermatol. 2010;10:6. doi: 10.1186/1471-5945-10-6.
3) Grieve K, Lui A et al. A randomized, assessor-blind, parallel-group, multicentre, phase IV comparative trial of a suffocant compared with malathion in the treatment of head lice in children.Australas J Dermatol. 2010 Aug;51(3):175-82. doi: 10.1111/j.1440-0960.2010.00622.x.
4) Detail-Document, Management of Head Lice. Pharmacist’s Letter/Prescriber’s Letter. September 2015.
5) Nontoxic head lice treatment. Available at http://nuvoforheadlice.com/test/?page_id=95
1. Canadian Immunization Guide. Available at http://www.phac-aspc.gc.ca/publicat/cig-gci/index-eng.php.
2. Personal communication - Saskatoon Public Health.
Essential oils are thought to be safe and usually well-tolerated when used short-term by inhalation. Some including bergamot, bitter orange, juniper, lavender, lemongrass, peppermint, ginger, Roman chamomile, and rosemary have been safely used when diluted and applied over small areas of unbroken skin. However, they can sometimes cause irritation of the skin, especially used at full strength.
Some, such as bergamot oil, can make the skin more likely to sunburn which increases the risk of skin cancer.
Applying large amounts of highly concentrated oils to a large surface of the skin or on broken skin can result in more of the oil being absorbed into the body which increases the chance of serious side effects.(2)
Essential oils may be unsafe when used orally. Oral use of essential oils is fairly uncommon; however, it does occur. Some essential oils can cause severe side effects when ingested in large undiluted amounts, including convulsions and kidney failure.
When a substance is taken orally, inhaled or absorbed through the skin, it brings up the question of interactions with prescription and over-the-counter (OTC) products. In general, the interactions between essential oils and other products are considered moderate when the oils are used topically or inhaled. However, caution is advised particularly with blood thinners such as warfarin. Some essential oils such as wintergreen can increase the risk of bleeding even when applied on the skin. Lavender can theoretically have additive effects when used with drugs for blood pressure as well as when used in combination with drugs that are taken for sleep. (2)
Aromatherapy is "the science of using highly concentrated essential oils or essences distilled from plants in order to utilize their therapeutic properties" (1) In aromatherapy, the essential oils are usually vapourized by heating or by adding the oil to a hot bath. Sometimes the oil is applied topically such as during massage, or to a specific areas such as the scalp or a painful joint. Less commonly, essential oils are taken orally (by mouth).
The vapourized essential oils of aromatic plants are believed to bring about effects such as feelings of relaxation and stress relief. Molecules from the vapour bind to receptors in the nose, which send signals to the brain. The effects of a particular odor can depend on psychological factors such as emotions, previous experiences, and expectations. Some constituents of vapours may pass into the bloodstream via the lungs and some might cross the blood-brain barrier and act directly on brain neurons. Inhaled aromas are thought to act much more quickly compared with application to the skin or taking them by mouth.
Clove oil has been used for the topical treatment of toothache because it contains eugenol which is sometimes used in dentistry for its pain relieving and antiseptic properties. The results of one study showed that clove oil gel is equally effective as benzocaine for local anaesthetic effect. (3)
There is some evidence that applying lavender oil in combination with the essential oils from thyme, rosemary, and
If you are unsure about interactions with your medication, check with your pharmacist before using any essential oil. Be careful not to use more than the amount recommended on the package.
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen BSP, MSc
Simkin, P, Klein, MC. Nonpharmacological approaches to management of labor pain. In:UpToDate, Lockwood, (Ed). ), UpToDate, Waltham MA, 2015. Accessed April 2015.
Aromatherapy monograph. In: Jellin JM, editor. Natural medicines comprehensive database online.
Stockton, CA: Therapeutic Research Faculty; c1995-2015 [cited 2015 April 27]. Available from: http://naturaldatabase.therapeuticresearch.com
Hay, IC, Jamieson, M, Ormerod, AD. Randomized Trial of Aromatherapy. Successful Treatment for Alopecia Areata. Arch Dermatol. November 1, 1998, Vol 134, No. 11 1998; 134(11):1349-1352. doi:10.1001/archderm.134.11.1349.
5. Algareer, A, Alyahya, A, Andersson, L. The effect of clove and benzocaine versus placebo as topical anesthetics. Journal of Dentistry, Volume 34, Issue 10, November 2006, Pages 747–750. doi:10.1016/j.jdent.2006.01.009
The treatment of choice for childhood insomnia is behaviour change, for example: strict bedtime routine, less attention to child’s demands for attention after bedtime or during the night, positive reinforcement, etc. If these measures are not successful, the next step could be medication.(1)
No melatonin products are licensed for use in children in Canada.(2) In fact, it is not registered for use in children anywhere in the world because it has not undergone the formal safety testing expected for a new drug, especially for long-term safety in children. (3)
There are a few studies which suggest short-term therapy with medication such as melatonin might be effective for sleep in certain children.(4,5) In these studies, which involved only a small number of children, there were no serious adverse effects. However, in animal studies testing melatonin supplements negative effects on the heart and blood vessels, the immune system, and other hormone-producing glands were reported.(3) In teenagers, there is concern that melatonin supplements might have a negative effect on the normal changes associated with puberty.(3)
For these reasons, melatonin is not recommended for use in most children. It may have a place in the treatment of children with developmental disorders such as cerebral palsy, autism, etc. under medical supervision.(1,4) Check with your doctor if you think melatonin might be appropriate for your child.
Melatonin is a hormone produced during the night in a small gland in the brain, called the pineal gland. Light causes the gland to decrease melatonin production and darkness causes it to increase production.(5) The pineal gland in most young people up to the age of 20 years produces melatonin in high levels. (4)
Melatonin works as a chronobiotic, which means it is capable of altering the timing of sleep. (3) Advocates of melatonin claim that it can be used to lengthen total sleep time, relieve or prevent daytime tiredness associated with jet lag, reduce the time needed to fall asleep and help reset the body's sleep-wake cycle. (4,5)
Studies on melatonin suggest that it is not useful as a treatment for insomnia for most people.(4,5,6) There are two exceptions: it may help people with delayed sleep phase syndrome (in which the typical patient has difficulty falling asleep and awakens late) and the small group of people with low melatonin levels. In these cases it appears to be safe when used short-term, up to three months or less. (4,6)
Side effects which have been reported are fatigue, headache, dizziness, irritability and abdominal cramps. In women during early menopause, melatonin has caused spotting or return of menstrual flow. People should not drive or use machinery for 4 to 5 hours after taking melatonin. (4)
Studies show that the intensity of household lighting in the few hours before their usual bedtime can affect a person’s sleep-wake cycle or circadian timing. This adds to the understanding that evening light exposure can affect human circadian timing and suggests that reducing household light exposure before bedtime may be a simple and safe way to decrease the time it takes to fall asleep. (7)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen BSP, MSc
medSask, May 2015
- Owens J. Behavioral sleep problems in children. In: UpToDate, Chervin R (Ed), UpToDate, Waltham, MA, 2015. Available at www.uptodate.com (by subscription). Accessed April 17, 2015.
- Health Canada LNHP Database. Available at http://webprod5.hc-sc.gc.ca/lnhpd-dpsnh/info. Accessed April 17, 2015.
- Kennaway DJ. Potential safety issues in the use of the hormone melatonin in paediatrics. J Paediatr Child Health. 2015 Feb 3. doi: 10.1111/jpc.12840. [Epub ahead of print]
- Melatonin. In: Natural Medicines Comprehensive Database. Stockton, CA: Therapeutic Research Faculty. [Updated on 02/15/2015; Accessed April 17, 2015]. Available at http://naturaldatabase.therapeuticresearch.com/nd/Search.aspx?cs=CEPDA&s=ND&pt=100&id=940&fs=ND&searchid=51262899. Accessed April 17, 2015.
- Procyshyn, RM, Barr, A. Minor Ailments – Insomnia. In: Gray Jean, editor. e-Therapeutics+ [Internet]. Ottawa (ON): Canadian Pharmacists Association; c2007 [updatedDec 2014; cited 2015 Apr 17]. Available from: http://www.e-therapeutics.ca. Also available in paper copy from the publisher.
- Bonnet, MH, Arand, DH. Treatment of insomnia. In: UpToDate, Benca, R(Ed), UpToDate, Waltham, MA, 2015. Available at www.uptodate.com (by subscription). Accessed April 17, 2015.
- Burgess HJ, Molina TA. Home lighting before usual bedtime impacts circadian timing. Photochemistry and Photobiology. Volume 90, Issue 3, pages 723–726, May/June 2014. Available at http://onlinelibrary.wiley.com/doi/10.1111/php.12241/full. Accessed April 17, 2015
Probiotics are live microorganisms used to replace or supplement the “good” bacteria in the bowel. Probiotics are most often obtained from cultured dairy products such as yogurt or kafir or from supplements. (1)
There is growing evidence that probiotics may help diarrhea, depending on what is causing the diarrhea. The probiotics that have the best evidence for benefit are species of Lactobacillus, Bidfidobacterium and Saccharomyces boulardii. These may be found alone or in various combinations in probiotic supplements. They are commonly promoted to strengthen the immune system and supply the intestines or vagina with beneficial germs. Their beneficial effects may include providing a protective barrier to the walls of the intestines and altering conditions to favour growth of good bacteria. (2, 3)
Diarrhea is most likely to respond to probiotics if diarrhea is caused by:
- Radiation to the lower abdomen and pelvis (used to treat cancer)
- Antibiotics used to treat infections (kill normal bacteria found in the intestines and vagina as well bacteria causing infections)
- Overgrowth of the intestinal tract by a bacteria called Clostridium difficile (C.dif)
- Stomach infection by a bacteria called Helicobacter pylori (H.pylori)
- Acute infectious diarrhea caused by viruses, bacteria or parasites
- Traveler’s diarrhea (may be caused by eating or drinking food and liquids contaminated with fecal material). Symptoms include diarrhea, cramps, and nausea that if untreated typically last from 2 to 6 days but can last for as long as a month.
Diarrhea associated with Irritable Bowel Syndrome (IBS) may respond somewhat to probiotics.
Diarrhea that occurs with conditions such as Crohn’s disease and ulcerative colitis does not seem to have a significantly favourable response to probiotics. (3)
To treat Antibiotic-Associated Diarrhea, take probiotics at least 2 hours after taking an antibiotic, otherwise the antibiotic can wipe out the probiotic organisms. The probiotic should be taken for the entire antibiotic course and up to a week afterward. (2)
To prevent Traveller’s Diarrhea, begin taking probiotics five days before travel and continue for the duration of trip. (2)
Long-term and intermittent use of probiotics for any reason appears to be safe for adults and children over 2 months of age. (2) However, use cautiously if you have a weakened immune system or if you are taking medication that affects your immune system.(3)
Prepared by Jean Macpherson, BSP; reviewed by Karen Jensen BSP, MSc
medSask, March 2015
1) Sartor, R B. Probiotics for gastrointestinal diseases. In: UpToDate, Lamont, JT (Ed), UpToDate, Waltham MA, 2015. Accessed March 2015.
2) Canadian Pharmacist’s Letter - PL Detail-Document, Comparison of Common Probiotic Products. Pharmacist’s Letter/Prescriber’s Letter. July 2012. Accessed March 2015.
3) Clauson, ER, Crawford P, What you must know before you recommend a probiotic. J Fam Pract. 2015 March;64(3):151-155. Nellis Family Medicine Residency Program, Nellis Air Force Base, Nev.
4) Forrester A. Gastrointestinal Conditions: Diarrhea. In e-therapeutics Complete – Minor Ailments. [Internet]. Ottawa (ON): Canadian Pharmacists Association; updated April 2013. Available from: http://www.e-therapeutics.ca. Also available in paper copy from the publisher. Accessed March 2015.
Current evidence finds that homeopathic remedies are no more effective for cough and cold than treatment with a placebo (a product with no active ingredients).1 They are rated as likely safe when taken by mouth or applied to the skin appropriately.2 Most homeopathic preparations contain little or no active ingredient. Therefore, it is unlikely that most homeopathic products will reduce cough and cold symptoms; on the other hand, it appears unlikely they will cause any harmful effects.
Since 2008 Health Canada has required the warning, "Do not give to children under 6”, be included on all cough and cold products that have certain active ingredients including: anti-histamines to treat sneezing and runny nose; anti-cough medications called anti-tussives: expectorants that loosen mucus; and decongestants to clear nasal passages. These medicines also require clear labelling for dosing for children 6 to 12 years, childproof packaging, and inclusion of a dosing device (such as a measuring cup or spoon) for all liquid forms. Although these non-prescription (OTC) medicines have been used for cough and cold for many years, there is little evidence to show that they are effective in children.3,4
So, what about the products on the pharmacy shelf that say they can be used for children under 9?
These are generally homeopathic products.5 Homeopathy is a pre-scientific practice based on two principles: “like cures like”, that is, the best treatment for a patient is a substance that, when given to a healthy person, produces symptoms similar to those of the patient; and “potentization,” which holds that multiple dilutions (adding water or other liquid to reduce the concentration of the active substance) and “succussions” (shakings) make the product increasingly more active because the liquid retains a “memory” of the initial substance. 5
Homeopathic preparations generally begin with minerals, plants, or animal substances that are crushed, mixed with a water or alcohol solution, and then potentized, usually well past the point at which any of the original substance remains. The resulting diluted liquid is applied to a sugar pill and allowed to dry or given in the liquid form with a dropper and applied to the tongue. 5
Homeopathic products are not regulated as closely as prescription medications and may contain other substances that could be harmful to certain people.5 Look for the DIN-HM, or Homeopathic Medicine number, on products sold in Canada. This number indicates that Health Canada has assessed the product for safety and quality.6 Homeopathic remedies should not replace medicines prescribed by your doctor for serious illnesses.
What can I give my child if they have a cough or cold?3,7
The cough and cold medications available treat the symptoms only, not the infection causing the symptoms. Here are a few safe ways to help your child get some relief from symptoms:
- Encourage rest
- Give lots of fluids, such as water, unsweetened juice, or clear soup.
- Use saline drops or sprays to clear nasal passages. These can be purchased over the counter or made at home by mixing ¼ to ½ teaspoon of table salt and a pinch of baking soda into 8 ounces of tap water (use within 24 hours). Nasal aspirators, devices which suck mucous out of the nostrils, can be used for infants and small children.
- Use a cool-mist humidifier or vapourizer to keep the air moist. This may help relieve cough and congestion.
- Soothe a sore throat with a cold drink, popsicles or ice cream. Older children can gargle with warm salt water.
- Give acetaminophen or ibuprofen if needed for discomfort caused by mild fever.
Keep in mind that symptoms of a cold will usually go away in about 6 to 10 days. If they don't, if symptoms worsen, or if your child appears sick and you are worried, consult a health care provider.3
Prepared by Jean Macpherson BSP Reviewed by Karen Jensen BSP, MSc
medSask, February 2015
- Atwood, KC. Homeopathy. In UpToDate, Aronson, MD (Ed) UpToDate, Waltham, MA, 2015. Available at www.uptodate.com by subscription. Accessed 09Feb2015.
- Homeopathy monograph. Natural Medicines Comprehensive Database. Available online by subscription. Accessed February 9, 2015.
- Children’s cough and cold medications: FAQ. Available at www.chealth.canoe.ca . Accessed 15Feb2015.
- Health Canada. Warning – Cough and Cold Medicine for Children. Available at http://www.hc-sc.gc.ca/dhp-mps/medeff/res/cough-toux-video-eng.php. Accessed 15Feb2015
- Weekes C. Think ‘approved’ homeopathic cold, flu remedies are safe? Available at http://www.theglobeandmail.com/life/health-and-fitness/health/think-approved-homeopathic-cold-flu-remedies-are-safe/article22385251/. Accessed 15Feb2015.
- Health Canada. About Natural Health Product Regulation in Canada.Available at http://www.hc-sc.gc.ca/dhp-mps/prodnatur/about-apropos/index-eng.php. Accessed 20Feb2015.
- Canadian Paediatric Society. Caring for Kids – Colds in Children. Available at http://www.caringforkids.cps.ca/handouts/colds_in_children. Accessed 20 Feb2015.
Symptoms of dry skin (xerosis) are scaling, itching and cracks in the top layers of skin. In most cases, skin becomes drier as we age, not because it lacks oil, but because it lacks water. Extreme environmental conditions can overwhelm the skin's natural protective barrier, causing water to evaporate. This is an important reason for dry skin among people who live in sunbaked desert climates and in cold-weather climates where excessively dry outdoor air and dry, heated indoor air also can cause dry skin.
Dry skin treatments are aimed at replacing and retaining water in the skin. When natural oils in the outer layer of skin are decreased the skin loses water. Although most cases have an environmental cause, certain diseases such as eczema and psoriasis can also significantly affect skin’s moisture balance.
Often itchy, dry skin is caused or worsened by cold weather and frequent bathing. The best way to prevent and treat dry skin problems is to moisturize. Moisturizers provide a seal over your skin to keep water from escaping.
General Self-Care Guidelines:
- Take a bath or shower no more than once daily. More frequent bathing can make the skin lose water.
- Use lukewarm (not hot) water.
- Limit bath and shower time to 15 minutes.
- Avoid harsh deodorant soaps (or limit their use to armpits, groin, and feet).
- Use non-soap cleansers, such as Aveeno® or Cetaphil® or mild soaps such as Neutrogena® or Dove®
- Pat (don't rub) the skin dry after bathing.
- Use a humidifier in the bedroom during the cold, dry seasons to help prevent dry skin.
Dry, rough, red skin:
- Apply moisturizer immediately after bathing, while the skin is still moist and then apply several more times a day.
- Thicker moisturizers such as Eucerin®, Cetaphil® or barrier creams work well to retain moisture in the skin.
- When choosing a moisturizer, look for oil-based creams and ointments, which work better than water-based lotions.
- Fragrance-free creams or ointments are preferred.
- If your skin symptoms have not improved after 7 to 10 days of treatment with moisturizers, step up to treatment with preparations containing higher concentrations of alpha-hydroxy acids (such as glycolic acid 10 % or lactic acid 5 % to 12 %) or urea (up to 10 %).
- If you have difficulty deciding which product is best for you, ask your pharmacist for advice.
- Products containing colloidal oatmeal (Aveeno® and others) are useful to help reduce itchiness.
- If itchiness is very bothersome, apply over-the-counter cortisone cream 0.5% to affected areas once or twice daily for up to 7 days. Check with your pharmacist or doctor if itchiness continues to be a problem or worsens.
- Topical antibiotics can be applied immediately to any cracks in the skin to help prevent infection.
- If signs of infection appear (increased redness, warmth, swelling, etc.), talk to your pharmacist or doctor.
Q. What is serotonin syndrome? How likely is it? What do I watch for and what do I do if I think I have it?
Serotonin (also sometimes called 5-HT) is a chemical produced by the body and found in the stomach and intestines, in the blood and also in the brain. It has many jobs in the body from helping to regulate the digestive system, blood pressure, body temperature and lung function, to affecting mood and behaviour (1).
Serotonin syndrome can occur when levels of serotonin build up in the body. It is a rare condition that can be caused by certain prescription drugs, illegal drugs and also some herbal supplements. The risk goes up when increasing doses of medications which affect serotonin or when combining these types of medicines.
Too much serotonin causes symptoms that can range from mild (shivering and diarrhea) to severe (muscle stiffness, fever and seizures). See Table 1 below for complete list of symptoms. Severe serotonin syndrome can be fatal if not treated.
Symptoms of serotonin syndrome usually occur suddenly, within 24 hours of starting a drug, adding a drug, changing a dose or overdosing:
- 50% of patients will have symptoms within 2 hours
- 75% of patients will have symptoms within 24 hours
- rarely can occur up to six weeks after stopping a long-acting drug (4)
Milder forms of serotonin syndrome usually go away within 24 to 72 hours of stopping medications that increase serotonin. In some cases medications to block the effects of serotonin already in your system can be used. However, symptoms of serotonin syndrome caused by some antidepressants could take several weeks to go away completely, because these medications remain in your system longer.
If you take any drugs or supplements that may cause serotonin syndrome (see Table 2 below), talk to your doctor or pharmacist about possible risks. Often the benefits of combining certain drugs will outweigh the risks but be aware of the possibility of serotonin syndrome and watch for symptoms especially during the first couple of days of treatment.
If your doctor prescribes a new medication, make sure he or she knows about all the other medications and supplements you're taking, especially if you receive prescriptions from more than one doctor.
Contact your doctor or go to an Emergency Department if you develop any of the symptoms listed in Table 1. Take a list of your medicines with you including vitamins and supplements. (2)
Table 1: Symptoms of Serotonin Syndrome
Table 2: Drugs and supplements which can contribute to serotonin syndrome
Antidepressants - Selective serotonin reuptake inhibitors (SSRIs)
Citalopram (Celexa), fluoxetine (Prozac), fluvoxamine (Luvox), paroxetine (Paxil) and sertraline (Zoloft)
Antidepressants - Serotonin and norepinephrine reuptake inhibitors (SNRIs),
Trazodone, duloxetine (Cymbalta) and venlafaxine (Effexor)
Antidepressant / Tobacco addiction
Bupropion (Wellbutrin, Zyban)
Antidepressant - Monoamine oxidase inhibitors (MAOI)
Antimigraine medications - Triptans
Almotriptan (Axert), naratriptan (Amerge), sumatriptan (Imitrex)
Antimigraine medications - other
Carbamazepine (Tegretol) and valproic acid (Depakene)
cyclobenzaprine (Flexeril), fentanyl (Duragesic), tramadol (Ultram)
Granisetron (Kytril), metoclopramide (Reglan), droperidol, ondansetron (Zofran)
Over-the-counter cough and cold medications
Dextromethorphan (Delsym, Mucinex DM, others)
St. John's wort, ginseng and nutmeg
LSD, ecstasy, cocaine and amphetamines
Produced by Jean Macpherson BSP, medSask medication information consultant. Reviewed by Karen Jensen MSc, BSP.
1) Boyer, EW. Serotonin syndrome. In UpToDate, Traub, SJ (Ed) UpToDate, Waltham, MA, 2015. Avabilable at www.uptodate.com by subscription. Accessed 09Jan2015.
2) Mayo Clinic Staff. Serotonin syndrome. Available at http://www.mayoclinic.org/diseases-conditions/serotonin-syndrome/basics/definition/con-20028946. Accessed 09Jan2015.
3) Dynamed – Serotonin syndrome. Available online at https://dynamed.ebscohost.com/ (by subscription). Accessed 09Jan2015.
4) Canadian Pharmacist’s Letter - PL Detail-Document, Facts about Serotonin Syndrome. Pharmacist’s Letter/Prescriber’s Letter. October 2014.
Q. I am taking a “blood-thinner”. Can I have an alcoholic drink on special occasions?
Moderate use of alcohol is considered safe for people taking anticoagulants (blood-thinners) if they have normal liver function.1,2,3 Anticoagulants taken by mouth include warfarin, dabigatran, rivaroxaban and apixaban.4 Moderate use is one drink per day for adult women and two drinks per day for adult men. One drink is a 12-oz beer, a 4-oz glass of wine, or a 1.5-oz glass of distilled spirits e.g. whiskey, vodka, gin.5
People taking anticoagulants should avoid consuming large amounts of alcohol over a short period a time (i.e., binge drinking). In the case of warfarin, this slows the elimination of warfarin from the body and increases the likelihood of bleeding. For all anticoagulants, intoxication increases the risk of falling which is also a risk for bleeding.1
If there is a substantial change in alcohol intake, lab values for INR (measure of how quickly blood clots) should be checked frequently. Any signs of bleeding including pain, swelling, headache, dizziness, weakness, prolonged bleeding from cuts, increased menstrual flow, nosebleeds, bleeding of gums from brushing, unusual bleeding or bruising, red or brown urine, or red or black stools should be reported to the doctor immediately.6
Prepared by Karen Jensen MSc, BSP. Reviewed by Terry Damm, BSP.
- Coumarin and related drugs + alcohol. In: Baxter K (ed), Stockley’s Drug Interactions. [online] London: Pharmaceutical Press. Available at http://www.medicinescomplete.com (by subscription). Accessed on 15Dec2014.
- Warfarin. Micromedex 2.0. Truven Health Analytics, Inc. Greenwood Village, CO. Available at: http://www.micromedexsolutions.com. Accessed 15Dec 2014.
- Alcohol-related drug interactions. Pharmacist’s Letter/Prescriber’s Letter 2008;24(1):240106.
- Douketis J, Bell A et al. Approach to the new oral anticoagulants in family practice. Part 2: addressing frequently asked questions. Can Fam Physician 2014;60:997-1001. Available at http://www.cfp.ca/content/60/11/997.long. Accessed 15Dec2014.
- Warfarin – ethanol. Drugs.com Interactions Checker. Available at www.drugs.com . Accessed 15Dec2014.
1. Q: If I have received FluMist® (the live influenza vaccine nasal spray), can I transmit the virus to others?
A. In clinical studies, nasal spray flu vaccine viruses have only rarely been passed on to close contacts. The risk of getting infected with a vaccine virus after close contact with a child who received the nasal spray flu vaccine is only 1 or 2 percent. (1) In addition, being infected is unlikely to result in flu symptoms because the viruses in the nasal spray are weakened. The vaccine viruses have not been shown to change into typical or naturally occurring flu viruses which could cause symptoms. (2)
2. Q: Is it dangerous for someone who is immunocompromised (i.e., has a weakened immune system due to medications or disease) to be in contact with people who have been given the FluMist® vaccine?
A: FluMist® vaccine recipients should avoid close contact with someone who has a severely weakened immune system (e.g., bone marrow transplant recipients requiring protective isolation) for at least two weeks following vaccination, because of the theoretical risk for transmission of the influenza virus. (2) People with lesser degrees of immunosuppression (diabetics, asthmatics who inhale corticosteroids, and people with autoimmune diseases such as rheumatoid arthritis, lupus, multiple sclerosis) can safely receive FluMist® . (1)
Disease modifying agents such hydroxychloroquine, sulfasalazine, or auranofin used to treat autoimmuine diseases are not considered immunosuppressive.(1) Prednisone in doses less than 20 mg daily (2 mg/kg daily for a child) or higher doses taken for less than 14 days is also unlikely to affect the immune system.(1) Medications which do cause a significant amount of immunosuppression and are listed in the Public Health Agency of Canada Immunization Guide include most cancer chemotherapies, injectable biologic agents used for rheumatoid arthritis, inflammatory bowel disease, etc. and medications used to prevent organ transplant rejection. For a complete list of drugs which would contraindicate the use of FluMist® , go to the Public Health Agency of Canada Immunization Guide (http://www.phac-aspc.gc.ca/publicat/cig-gci/p03-07-eng.php#a4).
3. Q: I am pregnant. Can I be in contact with someone who has had the FluMist® vaccine?
A: Yes. Pregnant women can be in close contact with others who have received the nasal spray vaccine. (1) Pregnant women should not however be given FluMist® for influenza prevention. They can safely receive the injectable formulations of the flu vaccine or the lower dose (9 ug) of the intradermal formulation of the vaccine. (1)
4. Q: Can FluMist® be administered with other vaccines?
A: FluMist® can be administered with or at any time before or after live attenuated or inactivated vaccines given by injection or by mouth. This is because the FluMist® exerts its effect on the immune system by a different route than the other vaccines. (1)
Note: this is not the case for injectable flu vaccines which if not given at the same time must be separate by at least a 28 day interval. (1) Live vaccines include:
- measles, mumps, rubella (MMR)
- chicken pox (varicella)
- yellow fever
Injections should be given, if possible, in opposite limbs. When multiple injections are given at one clinic visit, injections given on one limb should be separated by a distance of at least 2 cm. Different administration sets (needle and syringe) should be used for each injection. (1)
5. Q: Can I receive the influenza vaccine while I am breastfeeding?
A: Yes. Breastfeeding women can receive the injected or the nasal spray form of the vaccine. Receiving the influenza vaccine while breastfeeding reduces the risk of you getting sick and passing the illness to your baby. This is especially important if your baby is less than 6 months of age and cannot yet receive the flu vaccine. (4)
medSask October 2014.
- Public Health Agency of Canada. Statement on Seasonal Influenza Vaccine for 2014-2015. Available at http://www.phac-aspc.gc.ca/naci-ccni/flu-grippe-eng.php. Accessed October 2014.
- CDC. Seasonal flu shot. Available at www.cdc.gov/flu/about/qa/flushot.htm. Accessed October 2014
- CPhA. Influenza immunization guide for pharmacists 2014. Available at http://www.pharmacists.ca/cpha-ca/assets/File/education-practice-resources/Flu2014-Guide_EN.pd . Accessed October 2014.
- OTIS. Seasonal Influenza Vaccine (Flu Shot) during Pregnancy. Available at http://www.mothertobaby.org/fact-sheets-s13037#3. Accessed October 2014.
Q. Is the flu shot really effective? I’ve heard of people who get sick with the flu even though they have had the flu vaccination.
The effectiveness of the vaccine can vary from 60 to 85 per cent. It is more effective in people who are young and healthy, but may be less effective in older people. However, if a person gets the flu after influenza vaccination, it is usually a milder illness and less likely to require hospitalization. Antibodies to prevent influenza develop within 2 to 3 weeks after immunization in most healthy children and adults.
The National Advisory Committee on Immunization (NACI) states that healthy people aged 5-64 years benefit from influenza vaccination. Evidence also shows that flu vaccines benefit people of all ages and NACI now recommends flu shots for everyone 6 months and older, with particular focus on people at high risk of influenza-related complications or hospitalization and people capable of transmitting influenza to those at high risk.
It is estimated that between 10-20% of the population becomes infected with influenza each year. Rates of infection are highest in children aged 5-9 years, but rates of serious illness and death are highest in children under 2 years, people older than 65 years, and people with underlying medical conditions.
Aside from common reports of sore arms, low fevers and achiness after a flu shot, severe reactions are extremely rare in Canada. Those who have recently had a mild illness, with or without a fever, can still get the influenza vaccine.
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
- Government of Saskatchewan - http://www.health.gov.sk.ca/flu-common-questions
- Saskatoon Health Region -https://www.saskatoonhealthregion.ca/locations_services/Services/Influenza-Program/Documents/Influenza%20FAQs%20Web%20Aug212014_final.pdf
- Saskatoon Health Region - https://www.saskatoonhealthregion.ca/locations_services/Services/Influenza-Program/Documents/CD%2055%20Influenza%20fact%20sheet%202014-15.pdf
- Public Health Agency of Canada - http://www.phac-aspc.gc.ca/naci-ccni/assets/pdf/flu-grippe-eng.pdf
The Influenza Program in Saskatchewan begins on October 14th, 2014 and ends March 31st, 2015.(1)
The location and times of clinics where the vaccinations are available are listed on your Health Region’s website. You can find a link and a map to your region at http://www.health.gov.sk.ca/flushots as well as contact phone numbers.(2)
All Saskatchewan residents aged 6 months and older are eligible to get a free (publicly funded) seasonal influenza vaccine. (1) Non-publicly funded influenza vaccines may be available through workplaces or available for private purchase at pharmacies. The Ministry of Health does not reimburse the cost of privately-purchased vaccines.
It is estimated that between 10-20% of the population becomes infected with influenza each year. Rates of infection are highest in children aged 5-9 years, but rates of serious illness and death are highest in children under 2 years, people older than 65 years, and people with underlying medical conditions.(3)
The National Advisory Committee on Immunization (NACI) states that healthy people aged 5-64 years benefit from influenza vaccination. Evidence also shows that flu vaccines benefit people of all ages and NACI now recommends flu shots for everyone 6 months of age and older, with particular focus on people at high risk of influenza-related complications or hospitalization and people who can transmit influenza to those at high risk.(3)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
- Government of Saskatchewan - http://www.health.gov.sk.ca/flu-common-questions
- Saskatoon Health Region -https://www.saskatoonhealthregion.ca/locations_services/Services/Influenza-Program/Documents/Influenza%20FAQs%20Web%20Aug212014_final.pdf
- Public Health Agency of Canada - http://www.phac-aspc.gc.ca/naci-ccni/assets/pdf/flu-grippe-eng.pdf
FluMist® nasal spray is available for 2 to 17 year olds only and is dependent on supply. It is covered if administered at the immunization clinics which begin in October.(1) The location and times of clinics where the vaccinations are available are listed on your Health Region’s website. You can find a link and a map to your region as well as contact phone numbers at http://www.health.gov.sk.ca/flushots.(2)
FluMist® nasal spray should not be given to anyone with a weakened immune system or anyone with close contact to someone who has an extremely weakened immune system (e.g. bone marrow transplant recipients). Other people who should not receive FluMist® include:
- Anyone younger than 2 or older than 59
- Pregnant women
- Anyone with severe asthma or active wheezing in the last week
- Children on long-term aspirin therapy
- People who are very sick or have a very high temperature
- People with a past history of a severe allergic reaction to a previous influenza vaccine or any component of an influenza vaccine. These people should consult a public health nurse, their physician or nurse practitioner
- People who are allergic to eggs
- People who developed a neurological disorder called Guillain-Barré Syndrome (GBS) within 6 weeks of
a previous influenza immunization. (3)
Injectable vaccine is available for 18 years and older and for those who should not receive FluMist®. The 3 brands for IM vaccination this year are AGRIFLU™, VAXIGRIP® and FLUVIRAL®.(1)
Prepared by Jean Macpherson BSP; reviewed by Karen Jensen MSc, BSP
- Government of Saskatchewan - http://www.health.gov.sk.ca/flu-common-questions
- Saskatoon Health Region -https://www.saskatoonhealthregion.ca/locations_services/Services/Influenza-Program/Documents/Influenza%20FAQs%20Web%20Aug212014_final.pdf
- Public Health Agency of Canada - http://www.phac-aspc.gc.ca/naci-ccni/assets/pdf/flu-grippe-eng.pdf
Before your trip, consult with a travel medicine specialist at least one month before travel to ask about:
- Special vaccines that are recommended for specific destinations.
- First aid and medical kit containing regular and special medication for the trip – carry in hand luggage.
- Evacuation and travel insurance to cover health emergencies while abroad. (1)
Depending on your destination, some precautions can help you to stay healthy on your trip and arrive home the same way. The most common illnesses acquired on cruise ships are respiratory infections, sprains and strains, seasickness and gastrointestinal (GI) illness often caused by a virus called norovirus (previously called Norwalk virus) (1). Infections that occur on cruise ships can spread rapidly. With multiple ports-of-call and ever-changing staff members, diseases can be brought on board by infected individuals or in contaminated food and water.
Cruise ships that dock at ports in the United States are inspected for sanitation by Centre for Disease Control (CDC) officials to lessen the risk of gastrointestinal disease outbreaks on board. Travelers can obtain information on whether specific cruise ships meet sanitation standards from the CDC (www.cdc.gov/nceh/vsp/default.htm). (1, 2) Unannounced inspections are conducted on cruise ships travelling in Canadian waters. The inspections are conducted once per year during the cruise ship season which extends from April to the end of October. The results are matched with those from the CDC. Vessel Sanitation Program (VSP) (3)
The best prevention for respiratory infections such as the common cold is frequent hand-washing.
Some healthcare workers in Asia wear surgical-type face masks to prevent getting respiratory infections and these masks are increasingly used by travelers for the same purpose. In a study of their effectiveness, there was no difference in the frequency of colds between groups assigned to the mask or no mask. Subjects assigned to wear masks were much more likely to experience headaches while wearing the masks. (4)
Noroviruses cause fever and stomach upset including diarrhea and sometimes vomiting. They are very hardy and can withstand temperatures up to 60°C and can survive up to 2 weeks on surfaces such as tabletops. Outbreaks often occur in food service settings and settings in which people are in close contact such as cruise ships. The most effective prevention is hand washing with soap and water for at least 20 seconds and trying to not come in close contact with people who are ill. (6)
Motion sickness (sea sickness) is considered a form of dizziness and affects some people more than others. The symptoms of sea sickness include dizziness, nausea, burping, increased production of saliva and sweating. Hyperventilation (rapid, deep breathing) is common and can cause shortness of breath, skin tingling and feelings of impending doom. There isn't a good way to identify people at risk of motion sickness and some who have never had it before, may suffer from it in certain situations such as very rough seas.
Some strategies to help include; focusing on an object in the distance such as the horizon if you're on the sea, reserving a central cabin on a cruise ship or if this doesn’t work, trying an over-the-counter medication containing dimenhydrinate (such as Gravol). This is most effective if taken 30 to 60 minutes before travel, so it has time to work. Another option is scopolamine, a transdermal patch applied behind the ear. The benefit of scopolamine is that it lasts for 72 hours. It must be applied about four to twelve hours before travel is started and if another 3 days is required a new patch is applied behind the other ear. It shouldn’t be used longer than 6 days. Side effects for both kinds of medicine include drowsiness, blurred vision, dry mouth and in older adults possibly confusion. Scopolamine should not be used by people at risk of a less common form of glaucoma – angle closure glaucoma.(5)
Prepared by Jean Macpherson BSP, reviewed by Karen Jensen BSP MSc
medSask, September 2014
- International Travel Centre. www.saskatoonhealthregion.ca/locations_services/services/International-Travel. Accessed online September 22, 2014.
- Leder K, Weller P. Travel advice. In: UpToDate, Sexton, D(Ed), UpToDate, Waltham, MA, 2014. Accessed online September 22, 2014.
- Healthy Living. Cruise Ship Inspection Service. www.hc-sc.gc.ca/hl-vs/travel-voyage/general/ship-navire-eng.php. Accessed online September 22, 2014.
- McClain M, Sexton D. The common cold in adults: Treatment and prevention. In: UpToDate, Hirsch, M,(Ed), UpToDate, Waltham, MA, 2014. Accessed online September 22, 2014.
- Canadian Pharmacist’s Letter - Preventing Travel-Related Illnesses, Volume 2011, Course No. 317.
- Norovirus infection. In Dynamed online. EBSCO Information Services. Available at https://dynamed.ebscohost.com (by subscription). Accessed online September 22, 2014.
Applying drugs to the skin as a method to get them into the body (known as transdermal administration) was not recognized as a possibility until the 1920’s and it wasn’t until 1978 that a patch containing a drug for motion sickness was introduced. When drugs are taken by mouth they pass through the liver which can alter the structure of the chemical, also known as metabolism. Advantages of the transdermal method are that it allows the drug to remain unchanged by not having to first pass through the liver and avoids absorption and irritation problems in the stomach and intestines. This may result in needing lower doses and causing fewer side effects. The steady absorption of drug over longer periods also usually means less frequent dosing. Not all drugs can be incorporated into transdermal patches; they must be chemically suitable and non-irritating. Currently, drugs available in a transdermal patch are for hormone replacement, contraception, heart disease, smoking cessation, pain and brain disorders such as dementia and Parkinson’s disease. (1)
There are some disadvantages to transdermal patches such as skin reactions and less flexibility in doses than oral medications. Some other drawbacks to the use of medication patches are a delayed onset of action, the possibility of external conditions affecting drug release and absorption, and a potential loss of adhesion to the skin which could alter the dose. (2)
Transdermal patches are made up of several layers, including an impermeable backing (the layer visible when the patch is applied to a patient’s skin), a drug layer that contains the active ingredients, a rate-controlling membrane that controls the rate that the drug is released onto the skin, an adhesive layer that provides adhesion to the skin, and a protective cover (peel strip) to be removed before the patch is applied to the skin. (2)
There are some points to keep in mind when transdermal patches are used:
- Cutting the patch – Most patches should not be cut. Cutting can lead to inaccurate and sometimes dangerous doses caused by drug leaking from the cut edge. If a lower dose than is available is required, check with your pharmacist, nurse or doctor for instructions on whether it is possible to do it safely.
- · Patches that fall off – Patches should be applied on clean, dry skin. Patches should not be applied to the waistline or on areas where tight clothing can rub the patch off. If a patch falls off, a new one should be applied to a different site, in most cases. Some patches can be taped around the edges if they repeatedly fall off, but shouldn’t be covered completely with tape. Check with your pharmacist if you are having trouble with adhesion.
- Getting the patch wet – Most patches can be worn while showering, bathing or swimming. Care should be taken when drying off, so that the patch remains adhered to the skin.
- Dealing with irritated skin – The best way to avoid skin irritation is to change the site of application each time the patch is changed. If needed a mild steroid cream can usually be applied to the irritated site when the patch is changed.
- External heat – Using a heating pad or electric blanket, sitting in a sauna or taking a hot shower or bath while wearing a patch can alter the drug delivery and skin absorption.
- Illness – A fever can also affect the dose.
- Medical tests – Some patches contain aluminum in the backing and this can be a safety concern for people undergoing an MRI. The aluminum can conduct electrical current which can lead to burns, so the patch should be removed before the test.
- Writing on the patch – Most manufacturers do not recommend writing on patches. Some people do this to remember the date of application or make clear patches more visible, but it may tear the patch or the ink may be absorbed into the drug layer. It is suggested that the use of medical tape applied close to the patch with the required information is a better practice.
- Changing the patch – the used patch should be removed before applying a new patch as there may still be some drug left even after the recommended time and this can affect the dose.
- Discarding used patches – After the patch is removed, fold it in half with the sticky sides together. Follow instructions on proper disposal provided with the patch.
- Contact with the surface – If you inadvertently come in contact with the drug layer, wash the area with water. Hands should be washed with water before and after applying a transdermal patch. (2,3)
1. Perumal,O., Murthy, S.N., Kalia, Y.N., Turning Theory into Practice: The Development of Modern Transdermal Drug Delivery Systems and Future Trends, Skin Pharmacology and Physiology, 2013;26:331–342.
2. Durand, C., Alhammad, A., Willett, K., Practical considerations for optimal transdermal drug delivery, American Journal of Health-System Pharmacy, January 15, 2012 vol. 69 no. 2 116-124.
3. PL Detail-Document, Characteristics of Transdermal Patches. Pharmacist’s Letter/Prescriber’s Letter. August 2012.
Non-drug therapies for teething:
- Give the child something hard, smooth and clean to bite and chew on, such as a frozen facecloth.
- Safe teethers, cooled in the refrigerator before use, can be very effective in reducing symptoms.
- Rub the back of a small, cold spoon on the gum.
- Caution: Avoid long-term contact with very cold items. Do not place anything in the child's mouth that could be a choking hazard.
- Teething biscuits are not recommended because of their sugar content.
Recommended drug therapies:
- Oral pain relievers such as acetaminophen or ibuprofen can be used at the usual doses recommended for age and weight. These should never be rubbed on the gum.
Non-recommended drug therapies:
- Viscous lidocaine has been associated with serious adverse reactions (including death) in young children being treated for mouth pain, including teething. (3)
- The Canadian Dental Association does not recommend applying any local anaesthetics such as lidocaine or benzocaine to the gums, although several benzocaine-containing products are available without a prescription. These products only numb the area for 30–45 minutes. (1)
Benzocaine may disable the gag reflex if swallowed and the baby could choke on food.
Benzocaine has also been associated with a rare, but serious condition called methemoglobinemia, which results in the amount of oxygen carried through the blood stream being greatly reduced. In the most severe cases, methemoglobinemia can result in death. It has been reported with all strengths of benzocaine gels and liquids, including concentrations as low as 7.5%. The cases occurred mainly in children aged two years or younger who were treated with benzocaine gel for teething.
People who develop methemoglobinemia may experience:
- pale, gray or blue colored skin, lips, and nail beds
- shortness of breath
- fatigue; confusion
- headache; lightheadedness; and rapid heart rate
- In some cases, symptoms of methemoglobinemia may not always be evident or attributed to the condition. The signs and symptoms usually appear within minutes to hours of applying benzocaine and may occur with the first application of benzocaine or after additional use and immediate medical attention is required. (2)
- Homeopathic Hyland’s Teething Tablets were voluntarily recalled in 2010. The reason for the recall in Canada and the U.S. was a precautionary measure after the company and the U.S. Food and Drug Administration (FDA) conducted a review of the company’s adverse event reports and manufacturing processes. They have identified manufacturing processes that can be improved to ensure uniformity in dosage of the Belladonna 3X ingredient. According to U.S. FDA testing, Hyland's Teething Tablets may have posed a risk to children. A new formulation is now available according to the company, however there is no evidence that these products are effective for teething . (4)
About two-thirds of babies will have signs and symptoms accompanying the emergence of new teeth. Teething begins on average around 5 to 6 months of age. For a few days before a new tooth breaks through, the gums may be red, irritated, swollen and tender and babies may tend to produce more saliva and drool more than usual. The discomfort this causes may explain the irritability of the child, which may result in agitation, restlessness, crying and trouble sleeping or staying asleep. Other reported symptoms may include a decrease in appetite for solid food, increased thirst, mild increase in body temperature (up to 37.7°C), loose stools, ear rubbing and a stuffed up or runny nose.
Advice for Parents
- Continue to gently brush and clean the erupting tooth area to reduce the risk of secondary gum infection due to plaque sticking to teeth.
- Give child chilled teething toys (rings) or cool cloths to chew on. Ensure toys are lead free, washed, kept clean and stored in the refrigerator prior to use.
- Keep child well hydrated.
- Seek medical advice if symptoms are serious or persist for more than 24 hours, to rule out upper respiratory infection and other common conditions.
- First dental visit should occur within 6 months of eruption of first tooth or by age 1. (5)
- Dental Care: Teething. Minor Ailments in e-therapeutics Complete online. Available from: http://www.e-therapeutics.ca (by subscription). Accessed August 2014.
- Canadian Pharmacist”s Letter. PL Detail-Document, Safety of Oral Benzocaine Products. Pharmacist’s Letter/Prescriber’s Letter. May 2011
- Wright, JT. Anatomy and development of the teeth. In: UpToDate, Torchia, MM(Ed), UpToDate, Waltham, MA, 2014.Available at www.uptodate.com (by subscription). Accessed August, 2014.
- Health Canada Licensed Natural Health Products Database. Available at http://webprod5.hc-sc.gc.ca/lnhpd-bdpsnh/index-eng.jsp. Accessed August, 2014.
- Managing Discomfort Caused by Teething. J Can Dent Assoc 2013;79:d141
Ways to reduce the risk of catching “the itch”:
- Shower and towel dry well after swimming
- Do not swim where risk has been identified
- Use a pier or dock to enter the water. Larvae tend to stay near the shore
- Apply waterproof sunscreen before swimming. This may help to reduce the number of larvae penetrating the skin
- Do not attract birds to swimming areas
The Itch or Swimmer’s Itch is a skin rash that may appear several hours after swimming in lake or pond water (less frequently in salt water) that is infested with schisosome cercariae parasite. This parasite infects birds and mammals that frequent the water. Droppings from these animals contain the eggs of the parasite. The eggs hatch into larvae which infect snails. The snails release the larvae into the water. If the larvae come in contact with people, they can burrow under the skin where they die and cause an allergic reaction and a rash.
The rash appears within several hours after swimming and can range from a mild irritation to a severely itchy red rash. A tingling sensation may be felt as the skin dries off and the larvae start to burrow into the skin. The infection may last from two to five days and symptoms for as long as two weeks. Repeat infections are usually worse as people become sensitized to the larvae and have a stronger allergic reaction to them.
Symptoms may go away on their own in a few days. If the itching is bothersome, these treatments may be helpful:
- Over the counter hydrocortisone 0.5% cream
- Anti-itch lotions such as calamine lotion
- Cool compresses
- Baths with Epsom salts, baking soda or oatmeal
- Baking soda paste applied to itchy areas
- Oral antihistamines (ask your pharmacist to help you select the best one for you)
Try not to scratch. This worsens the rash and may cause infection. If signs of infection develop (increased redness, swelling, warmth), see your doctor for treatment.
- Mayo clinic. Swimmer’s itch. Available at www.mayoclinic.prg/diseases-condition/swimmers-itch. Accessed July, 2014.
- Government of Alberta. Swimmer’s itch. Available at https://myhealth.alberta.ca/health/Pages/conditions.aspx?hwid=abl0355. Accessed July 2014.
- Swimmer’s Itch. HealthLinkBC File #52 Available at www.healthlinkbc.ca/healthfiles/hfile52.stm. Accessed July 2014.
- Swimmer’s Itch FAQs. Centers for Disease Control and Prevention. Available at www.cdc.gov/parasites/swimmersitch/faqs.html. Accessed July 2014.
Prevention of swimmer’s ear can include the following (1):
- Keeping ears dry. Drain ear canals by tilting head to side and dry outer ear gently with a soft towel or with a blow dryer turned on low and held at least foot away.
- A homemade solution of equal parts of white vinegar with either water or isopropyl alcohol can be instilled in both ears before and after swimming.
- Watch for signs alerting swimmers to high bacterial counts and don't swim on those days.
- Don’t put foreign objects in your ears. Never attempt to scratch an itchy inner ear or dig out ear wax with a cotton swab or hairpin. This can irritate or break the skin and pack materials farther down the ear canal.
- Protect your ears with cotton balls when using hair dye
Swimmer’s Ear or otitis externa is an inflammation of the ear canal most commonly caused by a bacterial infection. It can affect any age group, although children 5 to 14 years have the highest incidence and it is estimated that 10% of people will develop it at some point in their life. (2)
It is more common during the summer months. This is because of increased humidity and increased exposure to outdoor water activities, both of which can affect the way that bacteria gain entrance to the ear. (2)
Extra moisture leads to softening of the skin and breakdown of the barrier of ear wax (cerumen) that protects the ear canal from infection. Cleaning too often with cotton swabs can remove the layer of cerumen and scratch the surface skin. If a piece of the swab or tissue is left behind they can harbour bacteria which cause infection. As well, devices such as hearing aids, ear buds and swim caps which cover the ear can increase the likelihood of infection.(2)
The symptoms of swimmer’s ear may occur rapidly and include tenderness of the outer structure of the ear, pain, itching, swelling, redness and possible hearing loss and jaw pain.(3)
Treatment is aimed at stopping the infection and reducing the pain.
- As long as there is no hole or tear in the eardrum, a solution of equal parts of white vinegar with either water or isopropyl alcohol can be used as an ear drop up to 4 times a day to help to dry out the ear canal and make it less appealing to the bacteria and fungi that cause swimmer’s ear.
- Children who have tubes in their ears should be seen by a doctor before treating.
- Prescription ear drops that contain an antibiotic with or without a steroid usually work quickly to stop the symptoms within 48 hours but should be continued for 7 to 10 days.
- Ibuprofen (e.g. Advil or Motrin) or acetaminophen (e.g. Tylenol) can be taken for pain. (2)
Prepared by Jean Macpherson BSP. Reviewed by Karen Jensen BSP, MSc.
Posted July 2014
1) Mayo Clinic. Swimmer’s Ear. Available at http://www.mayoclinic.org/diseases-conditions/swimmers-ear/basics/definition/con-20014723 Accessed June 25, 2014.
2) Goguen, LD External otitis: Pathogenesis, clinical features, and diagnosis. In UpToDate, Park, L (Ed), UpToDate, Waltham, MA, 2014.
Since babies with colic are reported to have increased amounts of gas-forming bacteria in their intestines it has been proposed that probiotics might reduce amounts of these organisms in babies’ intestines and help symptoms of colic. Research into the use of probiotics for colic has been rapidly gaining momentum, however the results of recent studies have been mixed. Some studies showed a positive effect on colic with the probiotic strain Lactobacillus reuteri in a select group of breastfed babies (1), but no positive effect in formula-fed babies. (2) Because of the lack of consistent, positive results, probiotics cannot be routinely recommended for babies with colic with any confidence that they will help.(3)
All babies, whether or not they have colic, cry more during the first three months of life than at any other time. Most people cannot agree on what constitutes an abnormal amount of crying. The length of time may vary from 42 minutes to 2 hours daily.
There is no standard definition for the term “colic.” For practical purposes, it is defined as crying for no apparent reason that lasts for more than 3 hours a day and occurs on more than 3 days a week in an otherwise healthy baby less than 3 months of age. Only 35 percent of infants considered to be "colicky" by their mothers met the "rule of three" criteria when parental diaries were kept. Symptoms resolve in 60 percent of infants by three months of age and in 80 to 90 percent of infants by four months of age. (4)
No single effective treatment for colic exists. Most guidelines recommend parental support and reassurance as the mainstay of management. The use of hypoallergenic (hydrolyzed) formulas for formula-fed babies or elimination of cow’s milk protein from the diet of mothers who are breastfeeding may possibly be effective for some babies, but not all. (2)
Probiotics are live microorganisms and are similar to the microorganisms that are found in the human gut. They are also called "friendly bacteria" or "good bacteria” and people take them to help to maintain the natural balance of organisms (microflora) in the intestines. (5)
Most researchers agree that more studies need to be done to determine if any group of babies with colic would benefit from probiotics. Probiotics are unlikely to be harmful, but there is little evidence to support their use.
In an editorial in the British Medical Journal (BMJ), W. Bennett a pediatric professor says, “Because of the lack of good evidence for treating colic, the question might be: “Should we be treating infant colic at all?” A great deal of accumulated clinical experience tells us that children with colic incur no serious long term effects from the disorder, and that symptoms abate with time.” (6)
1) Savino F, Cordisco L, Tarasco V, et al. Lactobacillus reuteri DSM 17938 in infantile colic: a randomized, double-blind, placebo-controlled trial. Pediatrics. 2010 Sep;126(3):e526-33. doi: 10.1542/peds.2010-0433.
2) Sung, V, Hiscock, H, Tang, MLK, Treating infant colic with the probiotic lactobacillus reuteri: double blind placebo controlled randomised trial. BMJ 2014;348:g2107
3) Bennett, WE, Probiotics and infant colic. BMJ 2014;348:g2286.
4) Turner T, Palamountain S. Infantile colic: Clinical features and diagnosis. In: UpToDate, Torchia, MM(Ed), UpToDate, Waltham, MA, 2014.
5) Probiotics. In Natural Standard database online. Available at www.naturalstandard.com (requires log-in and registration.
At this time, guidelines don’t recommend ASA for cancer prevention. They conclude that aspirin-related bleeding risks (especially in the brain and digestive tract) outweigh the benefits when it’s used for cancer prevention. Out of every 247 patients taking aspirin for 6 years, one cancer death is prevented, but 72 serious bleeds occur. (1)
Taking a low dose (75 – 100mg) of aspirin (ASA) every day may be of benefit for some types of cancer; however, there are very few studies at this time that show conclusively that ASA should be used for cancer prevention or treatment.
Some studies show that taking ASA may help lower the chance of getting some types of colorectal and other digestive tract cancers. Small benefits have also been observed for breast and prostate cancer. The results are not consistent and dosages and length of time needed to show a benefit are still unclear.(2)
- Recommendations to protect against colon cancer may include a “protective diet” which suggests avoiding processed and charred red meat,
- Eating vegetables - especially cruciferous such as cabbage and broccoli and folate-containing vegetables – especially leafy green vegetables
- Limiting calorie intake
- Avoiding excessive use of alcohol (women: no more than seven drinks per week and men: no more than 14 drinks per week). (3)
Since there are no updated guidelines, each person should discuss with their healthcare professional, the use of ASA for preventing diseases, the known risks and benefits and how they relate to each person individually. Because of the availability of screening methods such as colonoscopy for early detection of colon cancer, potential benefits of ASA use must be weighed against the potential adverse effects. (4)
In certain hereditary types of cancer conditions (e.g. Lynch syndrome) aspirin does decrease cancer incidence and should be considered a standard recommendation. (5)
Prepared by Jean Macpherson BSP and reviewed by Karen Jensen BSP, MSc
1) Canadian Pharmacist’s Letter - RUMOUR: Aspirin prevents cancer. August 2012 Rumour vs. Truth
3) Ahnen, DJ, Macrae, FA. Colorectal cancer: Epidemiology, risk factors, and protective factors. In UpToDate: Goldberg, RM, Lipman, TO (Ed) UpToDate, Waltham, MA, 2014.
4) Chan,A. NSAIDs (including aspirin): Role in prevention of cancer. In UpToDate: Feldman, M (Ed) UpToDate, Waltham, MA, 2014.
For best effect, the sunscreen should be applied first as it needs to be on the skin 15 to 30 minutes before sun exposure (1,2). Insect repellent is effective immediately and should be applied over the sun-screened area just before or after going outdoors (3,4).
It is not recommended to use a single product that combines insect repellent and sunscreen (5). Sunscreens must be applied liberally and frequently to provide maximum protection while insect repellents should be applied sparingly (1). Sunscreen should be applied to all areas exposed to the sun (1), while insect repellents should not be applied to the face (3,4).
It is recommended to avoid use of insect repellents on skin damaged by sunburn, cuts, rashes or other skin conditions (3,6). More absorption occurs through damaged skin which can lead to increased inflammation or an allergic reaction (6). Test any new insect repellent formulation on a small patch of skin first before applying to all exposed areas (5,7).
Prepared by Dorothy Sanderson, BSP; reviewed by Karen Jensen, BSP, MSc.
1. UpToDate - Selection of sunscreen and sun-protective measures
2. Sunscreens - http://healthycanadians.gc.ca/environment-environnement/sun-soleil/screen-ecrans-eng.php. Accessed June 2014.
3. Insect Repellents - http://healthycanadians.gc.ca/environment-environnement/pesticides/insect_repellents-insectifuges-eng.php. Accessed June 2014.
4. UpToDate - Prevention of arthropod and insect bites: Repellents and other measures
5. Insect Repellents - http://www.hc-sc.gc.ca/hl-vs/iyh-vsv/life-vie/insect-eng.php . Accessed June 2014.
6. CDC – www.cdc.gov/westnile/faq/repellent. Accessed June 2014.
7. Skin Cancer foundation – www.skincancer.org. Accessed June 2014.
Before starting to take aspirin (ASA) on a daily basis to prevent a heart attack or stroke, you should discuss the risks and benefits with your health care professional (1). For many people, the benefits do not outweigh the risks of taking ASA daily even at a low dose.
Heart attacks and certain kinds of strokes (ischemic strokes) occur when a blood clot forms and blocks the flow of blood and oxygen to the heart or brain. ASA works by interfering with the blood’s clotting mechanism so these clots do not form.
For people who have had a heart attack, a stroke or who have coronary artery disease, taking a low dose (81mg – 325mg) of ASA daily has been shown to help prevent a reoccurrence. This is called “secondary prevention”.
Preventing a first-time occurrence of one of these events is called “primary prevention”. In people who have not had a heart attack or stroke and who are at low risk for cardiovascular disease, even if they have a family history of these conditions, taking ASA daily may have more risk than benefit.
Approximately one first-time serious cardiovascular event is prevented for every 1000 patients on ASA for one year but at the cost of one serious bleeding event for every 1000 patients. The benefit seems to be even less for women. Treating 1000 women age 45 and up with ASA for 10 years may prevent only 2 or 3 ischemic strokes and even fewer heart attacks (3).
The specific risks with ASA are that it can cause dangerous bleeding into the stomach or into the brain (hemorrhagic stroke) (2). The first Canadian antiplatelet guidelines recommend against using ASA routinely for primary prevention in healthy people at low risk.
Taking ASA for primary prevention may be beneficial for some people. People at high risk for cardiovascular events, such as those with diabetes and are over the age of 40, and those with end-stage kidney disease; but only if they have a low risk of bleeding. Risk factors for bleeding include being female, having a previous bleeding episode and using medications such as non-steroidal anti-inflammatory drugs (e.g. ibuprofen, naproxen, diclofenac).
1) Hennekens, CH. Benefits and risks of aspirin in secondary and primary prevention of cardiovascular disease. In: UpToDate, Saperia GM (Ed), UpToDate,Waltham, MA, 2014.
2) FDA Consumer Health Information – www.fda.gov/ForConsumers/ConsumerUpdates
3) Aspirin for preventing cardiovascular events: who needs it? Pharmacist’s Letter/Prescriber’s Letter 2011; 27(8):270821.
Q. If I take acetaminophen while I’m pregnant, is my baby at risk of developing Attention Deficit Hyperactivity Disorder?
Acetaminophen (Tylenol, Atasol, store-brands) has generally been regarded as the drug of choice for minor pain and fever relief in pregnancy. Two recent studies from Europe have suggested there may be small increase in risk of ADHD (attention-deficit hyperactivity disorder) or similar conditions in children whose mothers take acetaminophen long-term (6 weeks or more), particularly during the last three months of pregnancy; however, more research is needed to confirm this risk (1,2).
An increase in major birth defects or miscarriage related to acetaminophen has not been shown (3). There may or may not be a link between acetaminophen and wheezing / asthma in the infant – some studies have shown an association but others have not (4). Overdose or prolonged use of high doses may result in liver damage to the unborn baby and other adverse effects (3).
Acetaminophen still seems safer than other drugs used for treating pain and fever in pregnancy when used in in normal adult doses for short periods of time. It is also a good choice for nursing moms as the amount that babies get from breast milk is less than doses given to babies, and adverse effects are rare. (4)
Keep in mind that it is important to treat fever in pregnancy. Fever during the first trimester has been associated with neural tube defects (e.g. spina bifida) and possibly other birth defects. In addition, fever during labor is a risk factor for seizures, brain disorders, cerebral palsy and death in the newborn. (6)
Prepared by Jean Macpherson, BSP, Medication Information Consultant.
Reviewed by Karen Jensen, BSP, MSc, Medication Information Consultant
2) Brandlistuen R, Ystrom E, et al. Prenatal paracetamol exposure and child neurodevelopment: a sibling-controlled cohort study. Int J Epidemiol. 2013 Dec;42(6):1702-13. doi: 10.1093/ije/dyt183. Epub 2013 Oct 24.
3) Acetaminophen monograph. Micromedex Healthcare Series. DRUGDEX System. Greenwood Village, CO: Truven Health Analytics, 2014. Available at http://www.thomsonhc.com/. Accessed April 17, 2014.
4) Acetaminophen monograph. Micromedex Healthcare Series. Reprotox. Greenwood Village, CO: Truven Health Analytics, 2014. Available at http://www.thomsonhc.com/ by subscription. Accessed May 15, 2014.
5) Canadian Pharmacist’s Letter PL - PL Detail-Document, Analgesics in Pregnancy and Lactation. Pharmacist’s Letter/Prescriber’s Letter. April 2014.
6) 3) Jamieson, DJ, Rasmussen, SA. Influenza and pregnancy. In: UpToDate, Barss,V (Ed), UpToDate, Waltham, MA, 2014. Available at www.uptodate.com by subscription. Accessed April 17, 2014.
Are TENS and ultrasound machines for home use safe and effective?
Chronic pain is one of the most common reasons for seeking medical attention and is reported by 20 to 50 percent of people who visit doctors. When conventional methods are not enough, many people look for other ways of treating pain. Ultrasound and TENS (Transcutaneous Electrical Stimulation) are non-drug methods which claim to help various types of pain. (1)
Good scientific research on ultrasound and TENS for pain relief is lacking and there appear to be varying rates of success for different conditions.
- It has been shown to provide some benefit for some people with chronic neck pain (2)
- TENS may provide short-term relief of pain and morning stiffness in people with osteoarthritis of the knee. The patients receiving TENS experienced more pain relief and had less need for pain relief medicine; however, these benefits occurred only while using the device. (3,4)
- It may help to interrupt or mask pain signals caused by phantom pain from an amputated limb. (5)
- It has been shown to be an effective therapy with minimal side effects in patients suffering from trigeminal neuralgia, a painful disorder of facial nerves not responding to conventional treatment. (6)
- TENS for treating fibromyalgia has had mixed results, but it may have some short-term benefit. (7)
- There are no conclusive positive results that there is any benefit to using TENS to treat cancer-related pain, although it has been widely used.(8)
- TENS is probably effective for reducing pain from diabetic neuropathy (nerve pain). (9)
- It has shown some benefit for women with painful menstrual periods that do not respond completely to drug therapy.(10)
- TENS, under medical supervision was shown to be an effective and safe treatment method for lower back pain during pregnancy. (11)
- There is only limited evidence that TENS reduces pain in labour. It may reduce severe pain and does not seem to have any impact (either positive or negative) on other outcomes for mothers or babies. (12)
TENS therapy involves applying electrodes to the surface of the skin and delivering low voltage electrical currents to the area. The electricity is usually generated by a battery-operated device. It is a non-invasive method and can be used by patients in their homes. Most TENS devices offer variable frequency, intensity, pulse duration and type of output (burst or continuous). Regular TENS (high frequency, short pulse duration, low intensity) produces a sensation of prickling or tingling like “pins and needles” under the electrodes and acupuncture-like TENS produces muscle twitches. (1)
TENS can be tested during a home trial or as a supervised trial when working with a physical therapist. Given the uncertainty about the amount of electrical stimulation most likely to help in an individual patient, a serious trial of TENS requires many days and should test various sites and timings of stimulation, as well as a variety of amplitudes, frequencies, and patterns.
People with the following must not use a TENS machine (13, 14):
- When the cause of the pain is not known or is not diagnosed.
- Pacemakers or ICD’s (implantable cardioverter-defibrillator).
- Epilepsy or certain types of heart disease.
TENS machines are available in widely varying price ranges and can cost up to hundreds of dollars. Many advertisements make unsubstantiated claims about their effectiveness. A supervised trial by a medical professional or a physiotherapist would be advisable before purchasing one for use at home.
The term "ultrasound" refers to sound waves of a frequency greater than that which the human ear can hear. Ultrasound machines generate sound waves which cause microscopic vibrations in tissues increasing heat and causing a warming effect. It is usually used in combination with other non-drug treatments and its beneficial effect is thought to be due to the heating of deep tissues. (15)
Despite being widely used for the treatment of many muscle and pain syndromes, few studies have evaluated the therapeutic effect of ultrasound.
- Ultrasound therapy may reduce pain and improve function in patients with some types of shoulder pain and may help to aid in muscle relaxation before exercise. (16)
- It has no proven benefit and is not recommended as a therapy for treating osteoarthritis and is not routinely used. (3)
- Ultrasound has been used to promote recovery after nerve and tendon injuries.
- It has been used to treat carpal tunnel syndrome by raising tissue temperature while reducing pain. Deep, pulsed ultrasound has been reported to decrease pain and improve sensory loss, nerve conduction parameters, and strength. (17)
- It has been used in combination with stretching exercises to reduce pressure when treating bursitis of the hip.(18)
Ultrasound without medical supervision should NOT be used for:
- Patients who have dulled reflexes or decreased sensitivity to pain and heat
- Pregnant or potentially pregnant patients. (Overheating and damage to the fetus could result. The fetus is at particularly high risk during the first trimester.)
- Pain in reproductive organs
- Treatment in the area of the eye
- Any region of diminished blood flow (except at low intensities for wound healing)
- The brain, spinal cord or large subcutaneous peripheral nerves
- Neoplastic (cancerous) tissues as there is some evidence that temperatures less than 42°C, may stimulate tumor growth or promote spread of the cancer
- People who have pacemakers or ICD’s
- Blood vessels in poor condition (the vessel walls may break open)
- Patients suffering from heart disease (might result in reflex tightening of the blood vessels in the heart)
- People at risk of blood clots (a partially disintegrated clot could result in blockage of the arterial blood supply to the brain, heart or lungs)
Ultrasound machines are available for use at home and can range in price up to hundreds of dollars. It is important that patients understand how to correctly use their ultrasound machine because improper technique can, at best, reduce the benefits of ultrasound and, at worst, result in tissue damage. (19)
Provided by Jean Macpherson, BSP Reviewed by Karen Jensen BSP, MSc
April 4, 2014
1) Rosenquist, EWK. Overview of the treatment of chronic pain. In UpToDate, Rosenquist, EWK (Ed), UpToDate, Waltham, MA, 2014.
2) Anderson, BC, Isaac, Z, Devine, J. Treatment of neck pain. In UpToDate, Rosenquist, EWK (Ed), UpToDate, Waltham, MA, 2014.
3) Kalunian, KC. Nonpharmacologic therapy of osteoarthritis. In UpToDate, Tugwell, P(Ed), UpToDate, Waltham, MA, 2014.
4) Dynamed - Degenerative joint disease of the knee. Accessed March 2014.
6) Dynamed – Trigeminal neuralgia. Accessed March 2014.
7) Goldenberg, DL. Treatment of fibromyalgia in adults not responsive to initial therapies. In UpToDate, Schur, PH(Ed), UpToDate, Waltham, MA, 2014.
8) Strada, EA, Portenoy, RK. Psychological, rehabilitative, and integrative therapies for cancer pain. In UpToDate, Abrahm, J (Ed), UpToDate, Waltham, MA, 2014.
9) Feldman, McCulloch, DK. Treatment of diabetic neuropathy. In UpToDate, Shefner, JM, Nathan, DM, (Ed), UpToDate, Waltham, MA, 2014.
10) Smith, RP, Kaunitz, AM. Treatment of primary dysmenorrhea in adult women. IN UpToDate, Barbieri, R(Ed), UpToDate, Waltham, MA, 2014.
11) Keskin EA1, Onur O, Keskin HL, Gumus II, Kafali H, Turhan N. Transcutaneous electrical nerve stimulation improves low back pain during pregnancy. Gynecol Obstet Invest. 2012;74(1):76-83.doi:10. 1159/000337720. Epub 2012 Jun 21.
12) Dowswell T, Bedwell C, Lavender T, Neilson JP. Transcutaneous electrical nerve stimulation (TENS) for pain relief in labour. Cochrane Database Syst Rev. 2009 Apr 15;(2):CD007214. doi: 10.1002/14651858.CD007214.pub2.
13) Risk of interference from transcutaneous electrical nerve stimulation on the sensing function of implantable defibrillators. Holmgren C. Carlsson T. Mannheimer C. Edvardsson N. Pacing & Clinical Electrophysiology. 31(2):151-8, 2008 Feb. [Journal Article] UI: 18233966
15) Chou, R. Subacute and chronic low back pain: Pharmacologic and nonsurgical interventional treatment. In UpToDate, Rosenquist, EWK (Ed), Rosenquist, EWK (Ed), UpToDate, Waltham, MA, 2014.
16)Dynamed - Impingement syndrome of rotator cuff. Accessed April 2014.
17) Kothari, M. Treatment of carpal tunnel syndrome. In UpToDate, Shefner, JM,(Ed), UpToDate, Waltham, MA, 2014.
18) Anderson, BC. Trochanteric bursitis. In UpToDate, Isaac, Z, (Ed), UpToDate, Waltham, MA, 2014.19) Health Canada. Occupational Health and Safety. Accessed online March 2014. http://www.hc-sc.gc.ca/ewh-semt/pubs/radiation/safety-code_23-securite/index-eng.php
Medical grade honey has evidence to support its use in burn management and may shorten the time it takes a burn to heal. (1) Medihoney, an OTC honey dressing which has been sterilized, is available in Canada. Not all honey products are sterile and some may contain clostridium spores and other contaminants. Since not all honeys are the same and do not possess the same therapeutic advantages, do not treat wounds with regular honey sold in grocery stores. The use of butter is not recommended due to the increased risk for infection. (2)
Overview of burn treatment
In general, first and second degree burns may be managed through self-care, unless the burn area is large, involves the eyes, ears, face, hands, feet or mucous membranes (lips, mouth, inside nose) or the patient is elderly, has diabetes, multiple medical conditions, or has a weakened immune system. Chemical, electrical, or inhalation burns require medical attention and should not be treated with self-care. (2)
Burns occur when some or all of the cells in the skin or other tissues are destroyed by heat, cold, electricity, radiation, or caustic chemicals. The most common type of burn in children is from a scald injury; in adults, the most common burn occurs from a flame. Burns are classified according to the depth of tissue injury:
- superficial (first-degree)- painful, red and warm, area turns white when touched, no blisters, moist
- partial-thickness (second degree) - painful, red, moist, with blisters, hair still intact
- full thickness (third degree) - painless with no sensation to touch, skin is pearly white or charred, dry and may appear leathery
- involving muscle and/or bone (fourth degree). (3)
Initial treatment of minor burns consists mainly of removing anything covering the burn area, cooling, simple cleansing, and applying a dressing. Medication to treat pain may also be necessary. Check with your doctor to see if you need a tetanus shot (a booster is recommended if it is longer than 5 years since the last shot). The goals of treating minor burns are to relieve symptoms, promote healing by protecting the burn from infection or further injury, and to decrease the risk scarring. (2, 4)
Cooling — After any clothing, jewelry, and loose dirt is removed, burn wounds can be cooled with room-temperature or cool tap water to provide some pain relief and limit tissue injury. Cool running water for about 20 minutes is recommended. Sterile saline or sterile water can be used, but are not necessary. Ice is not recommended as it can reduce blood flow to the area and worsen the injury or slow healing. Applying sterile saline-soaked gauze, cooled to around 12°C (55°F), is another effective means of cooling. (2, 3)
Cleaning — Burn wounds should be cleaned using only mild soap and tap water. Avoid skin disinfectants such as povidone-iodine as these can hinder healing. Gentle removal of dead skin will help in the healing process. Small blisters can be left intact. Large blisters should be seen by a doctor for assessment. (2, 4)
Pain management – Acetaminophen, ibuprofen or naproxen can be used for pain and should be given regularly for the first day or two. Since a burn can worsen over 24 to 48 hours, it should be reassessed frequently as the severity may have been underestimated at first. Topical anesthetics such as benzocaine or lidocaine although cooling, are not recommended because they can cause irritation or allergic reactions. (2)
Manage Itching - Itching is a common problem while burns are healing. Antihistamines such as diphenhydramine (Benadryl) or cetirizine (Reactine) can help combat itching. Bathing in water with baking soda or oatmeal may help. Other topical treatments for itching include: aloe vera, petrolatum-based (Vaseline) creams, cocoa butter, mineral oil and oatmeal containing creams (Aveeno). (1) Topical steroids such as hydrocortisone can be applied to unbroken skin or burns that are healing well to help with itching. (2,5)
Antibiotic skin creams - Minor burns without broken blisters or cracked skin do not require a topical antibiotic. A topical antibiotic (e.g. Polysporin, generic brands) should be applied to burns where the skin is broken (e.g., where blisters have opened and exposed a layer of skin underneath). (2,5)
Dressings - Burns heal best in moist, not wet, conditions. To maintain a moist environment, apply a nonsticky dressing or skin protectant such as allantoin, cocoa butter or petrolatum to superficial burns. (5)
For small burns with minor blistering, a hydrocolloid dressing (DuoDERM, TegaDerm,) can be used to protect the burn and keep it moist. (2)
- DynaMed [Internet]. Ipswich (MA): EBSCO Information Services. Minor burns [Updated 2013 May 20; cited 2014 March 28] Available from http://search.ebscohost.com/login.aspx?direct=true&site=DynaMed&id=113862. Registration and login required.
- PL Detail-Document, Management of Minor Burns. Pharmacist’s Letter/Prescriber’s Letter. April 2012.
- Rice, PL, Orgill, DP. Classification of burns. In: UpToDate, Jeschke, MG(Ed), UpToDate, Waltham, MA, 2014
- Morgan, ED, Miser, WF. Treatment of minor thermal burns. In: UpToDate, Moreira, ME (Ed), UpToDate, Waltham, MA, 2014
- Tenenhaus, M, Rennekampff, H. Local treatment of burns: Topical antimicrobial agents and dressings. In: UpToDate, Jeschke, MG(Ed), UpToDate, Waltham, MA, 2014
The benefits of pet ownership are well documented from lowering blood pressure to improving symptoms of depression. However, although the risk is small, it is possible for your pet to make you sick. This is mainly a concern for people whose immune systems are impaired, for older adults, children under 5 and pregnant women.
Diseases that are transmitted from animals to humans are called zoonoses. Many of the risks associated with zoonoses can be lessened by good hygiene after handling pets, careful pet selection, and proper pet care. Adult pets are generally safer than younger animals, since they are less likely to be involved in playful activities that include scratching and biting. Children are at highest risk for infection because they are more likely to have close contact with pets and less likely to understand the importance of hand washing after contact with animals.
Although both dogs and cats have been implicated in transmission of zoonoses to their owners, risk of transmission from contact is low. Infections which can potentially be contracted from a cat or dog include:
- Rabies from contaminated saliva entering the blood stream through bites or scratches.
- Superficial surface skin infections resulting from bites and scratches
- Fungal skin infections such as ringworm transferred by direct contact with the skin of an infected animal
- Toxoplasmosis, a disease caused by a parasite acquired by handling cat feces – dangerous for unborn babies if mothers are exposed
- Salmonella (bacteria which cause food poisoning) from contaminated feces of either cats or dogs
- Tick borne diseases such as Lyme disease if a pet brings these insects into contact with people.
Rodents, including hamsters, gerbils, guinea pigs, mice and rats are becoming more common pets. Ringworm is the most common zoonotic disease spread to humans from rodents and is spread by skin to skin contact. Transmission of infections which enter the body usually occurs through bites or exposure to bacteria in the feces.
Pet reptiles and amphibians such as snakes, turtles, lizards, geckos, and frogs can spread Salmonella infections which can cause fever, stomach upset and bloody diarrhea in humans. The organism is present in the feces and on the skin or shells of these animals.
Exotic pets such as monkeys, ferrets and hedgehogs can also spread disease to humans, most commonly fungal skin infections from direct contact and E. coli or Salmonella from handling of feces.
Some simple precautions can greatly reduce the possibility of your pet making you sick.
- Pets should be seen by a veterinarian on a regular basis and treated promptly for diarrhea and skin infections
- Cats and dogs should be vaccinated for rabies
- Pets should be fed high quality commercial food and should not eat raw meat or eggs. They should not be allowed to eat garbage, feces, or hunt
- Pets should not be allowed to drink non-potable water such as surface water or toilet water
- Young pets present a greater risk for disease than older pets, as they are more likely to engage in playful nipping and biting, behavior which may transmit bacteria
- Owners should wash their hands following contact with their pet or cleaning of their cages.
- Pregnant women should not handle cat litter boxes.
- Ringworm and minor skin infections can be treated with over-the-counter products. Ask your pharmacist for help in selecting the appropriate medication.
Prepared by Jean Macpherson, BSP. Reviewed by Karen Jensen BSP, MSC
- Kotton, CN. Zoonoses from dogs. In: UpToDate, Sexton, DJ (Ed),UpToDate, Waltham, MA,2013.
- Kotton, CN. Zoonoses from cats. In: UpToDate, Sexton, DJ (Ed),UpToDate, Waltham, MA,2013.
- Kotton, CN. Zoonoses from pets other than dogs and cats. In: UpToDate, Sexton, DJ (Ed),UpToDate, Waltham, MA,2013.
- Public Health Agency of Canada. Injuries associated with... DOG BITES AND DOG ATTACKS. Available at http://www.phac-aspc.gc.ca/injury-bles/chirpp/injrep-rapbles/dogbit-eng.php. Accessed December, 2013.
- Pawsitive thinking. (2013, November). Wellness Letter. University of California, Berkeley, Volume 30 (Issue No. 3). P.1-2.
Saskatchewan health officials are reporting increasing influenza activity in the province.
The 2013/14 flu season started late in Saskatchewan, but has already resulted in hospitalization for some people with severe illness. The level of influenza activity is expected to increase into the new year.
The Ministry of Health for Saskatchewan is encouraging Saskatchewan residents to get a flu shot if they haven’t already done so, and practice good hand hygiene to help them avoid getting sick. In Saskatchewan and across Canada, H1N1 is the predominant strain causing illness this flu season. This strain is included in this year’s flu vaccine. The injectable and nasal mist vaccines are still available and can be ordered through pharmacies, if necessary.
For Saskatoon and area vaccine supply information, please visit www.4flu.ca. If you live outside of Saskatoon, check your health region website or call HealthLine 811 to find out when and where vaccinations will be available near you.
Prepared by medSask, Your Medication Information Service
Updated Jan. 23, 2014
Q. Do generic drugs actually work as well as brand name drugs? I’ve heard on the news (again!) that someone did much worse on a generic drug compared to the brand name drug.
A recent news article, found here, has once again sparked the debate of whether generic drugs are just as good as brand name drugs. To answer this question, it is important to understand the approval process of drugs in Canada to see how generic drugs come to market.
Health Canada decides which drugs are allowed to be sold in Canada. Drug manufacturers, whether in Canada or internationally, must prove their product contains exactly what is labelled and abide by strict “Good Manufacturing Practice” guidelines. Both brand name drugs and generic drugs are subject to the same criteria; there are not two separate approval processes.
Generic drugs must have the same amount of active ingredient as the brand name drug, but are allowed to have different non-active ingredients or “fillers”, which are ingredients that help hold the tablet together, make it easier to swallow, make it gentler on the stomach, or preserve the drug, etc. If the generic drug is produced with different fillers, then the manufacturer must prove “bioequivalence” – that is, they must prove that the product delivers the same amount of drug to the body over a period of time compared to the brand name product. In most cases, if the generic drug has the same fillers (and the same amount), a bioequivalence test is not necessary (1).
To perform a bioequivalence test, usually between 30 and 70 healthy people are tested in two groups. An individual will receive either the brand or generic drug and the amount absorbed is measured. The procedure is then repeated with the other drug. If the drugs are absorbed and removed by the body at a similar extent over a period of time, they are deemed bioequivalent (2). So, what is “a similar extent”?
People commonly claim bioequivalence requirements are too loose, that the amount of active ingredient in a generic drug is allowed to be from “80 to 125%” of that in the brand name product; thus, a possible 45% variance in the active ingredient is allowed. This is untrue; the “80 to 125%” figure refers to a statistical term called the 90% confidence interval for the “area under the curve (AUC)” (3). The confidence interval takes into account the absorption and excretion differences between people in the study, and the AUC is a measure of the concentration of a drug over time as it is absorbed into the body and then slowly removed from the body. Putting it together, this means that when a generic drug is taken, the entire AUC (taking into account the differences between people being studied), must always fall between a small range of values which lie entirely between 80 to 125% of the stated amount, or it fails the equivalency test; practically, this means the actual variance is less than 5% (4), with studies finding an average variance of 3-4% (5).
The graph below may help illustrate this point (3):
Only “A” passes the bioequivalence test, since the entire range of AUC values for individuals in the study lie between 80 and 125%. The rest fail because their range of values cross the acceptable variance.
A variance of 3-4% must be put into perspective; different batches of the same brand name drug are allowed to have the same variance (6), thus, the potential variation from switching to a generic version is no different than the variation of receiving the same brand at different times.
Some argue that since some drugs must be dosed very accurately, the 3-4% variation can be important. This is true, and so Health Canada has labelled some drugs as “critical dose drugs”, which means the range of AUC values must lie between 90 and 112%, rather than 80 to 125% (7); thus, the range in the graph above would be even tighter, creating an even smaller allowable variance.
Another misconception is that since generic drugs are less expensive than their brand name counterparts, they must be of poorer quality. When a company develops a new drug, they spend a substantial amount on research and development of the drug, and must perform expensive studies to prove the safety and efficacy of the new drug. This takes many years and an average of $1.1 billion (8). The brand name manufacturers are rewarded for this investment with a patent – a time during which no other manufacturer can produce the drug. The price set by the brand name manufacturer factors in the money spent in research and development. Once patent expires, the generic drug companies are free to produce the drug. Since they do not have to invest in research and development they can bring their version of a drug to market for a much lower cost—it has nothing to do with a lower quality product or substandard manufacturing.
The advantage of generic drugs versus brand name drugs is lower cost. In Canada, since the government helps pay for many people’s medications, when a lower cost version is routinely given, it amounts to significant savings for the struggling health care system; approximately $7 billion was saved in 2010 (9). Switching to generic medications to save all this money has NOT caused an increase in harm to patients; two large studies show no differences in outcomes when using generic drugs for patients with cardiovascular disease (10) or infections (11).
Certainly, from time to time, there are reports that a switch from one brand to another (from brand name to generic or from one generic to another generic) result in adverse effects. This means that someone could experience a side effect that did not happen before the switch, or the drug may not work as well--but this is very rare. Extra caution is suggested when switching between brands of “critical dose drugs” (e.g., anti-seizure drugs, warfarin, lithium, thyroid hormone, etc.) and extended release formulations (12). If the medication does not seem to be working as well as normal or if side effects appear after a switch, contact your doctor. However, when starting on a new medication, a generic version is just as good as the brand version (13).
If generic drugs are just as good, why are there reports of people doing worse on them? They may have different fillers, so if the generic version contained something like a sulfite and the brand name did not, an allergic reaction could be possible, though very rare. More likely, there is significant bias at play; if a person has negative expectations about a generic drug, any issue will likely be blamed on the generic, instead of the real cause. One has to consider that in almost all cases, no difference is noticed; these cases don’t make it to the news.
For the vast majority of people, generic drugs are just as good as the brand name drugs, and have enormous cost saving potential for our health care system and need to be utilized as much as possible. Be confident taking a generic medication, as Health Canada has stringent regulations in place to ensure only safe and effective products are marketed.
Prepared by Terry Damm, BSP
Reviewed by Carmen Bell, BSP; Darcy Lamb, BSP, MSc; Karen Jensen, BSP, MSc
1. Health Canada. Biopharmaceutics Classification System Based Biowaiver. Accessed online Dec 2013. http://www.hc-sc.gc.ca/dhp-mps/alt_formats/pdf/consultation/drug-medic/bcs_draft_guide_ebauche_ld_scb-eng.pdf
2. Canadian Generic Pharmaceutical Association. Bioavailability and Bioequivalence – What Are They? Accessed online Dec 2013. http://www.canadiangenerics.ca/en/resources/docs/09.16.13%20Bioequivalence2013_Eng.pdf
3. Generic drug variability. Pharmacist's Letter/Prescriber's Letter 2008;24(7):240704.
4. The Canadian Agency for Drugs and Technologies in Health. Similarities and Differences Between Brand Name and Generic Drugs. Accessed online Dec 2013. http://www.cadth.ca/en/resources/generics/similarities
5. Davit BM, Nwakama PE, Buehler GJ, et al. Comparing generic and innovator drugs: a review of 12 years of bioequivalence data from the United States Food and Drug Administration. Ann Pharmacother. 2009;43(10):1583-1597.
6. Health Canada. Good Manufacturing Practices Guidelines. Accessed online Dec 2013. http://www.hc-sc.gc.ca/dhp-mps/alt_formats/pdf/compli-conform/gmp-bpf/docs/gui-0001-eng.pdf
7. Health Canada. Comparative Bioavailability Standards: Formulations Used for Systemic Effects. Accessed online Dec 2013. http://www.hc-sc.gc.ca/dhp-mps/prodpharma/applic-demande/guide-ld/bio/gd_standards_ld_normes-eng.php#a18.104.22.168
8. Deloitte. Measuring the Return from Pharmaceutical Innovation 2012. Accessed online Dec 2013. http://www.deloitte.com/view/en_GB/uk/research-and-intelligence/deloitte-research-uk/deloitte-uk-centre-for-health-solutions/b47f30374ca4b310VgnVCM2000003356f70aRCRD.htm
9. Canadian Generics Pharmaceutical Assocation. Accessed online Dec 2013. http://www.canadiangenerics.ca/en/
10. Aaron S. Kesselheim, MD, JD, MPH, Alexander S. Misono, BA, Joy L. Lee, et al. Clinical Equivalence of Generic and Brand-Name Drugs Used in Cardiovascular Disease. JAMA. 2008 December 3; 300(21): 2514–2526.
11. Snyman JR, Schoeman HS, Grobusch MP, Henning M, et al. Generic versus non-generic formulation of extended-release clarithromycin in patients with community-acquired respiratory tract infections: a prospective, randomized, comparative, investigator-blind, multicentre study. Clin Drug Investig. 2009;29(4):265-74.
12. Lewek, P., Karsas, P. Generic drugs: The benefits and risks of making the switch. The Journal of Family Practice. Accessed online Dec 2013. http://www.jfponline.com/index.php?id=22143&tx_ttnews[tt_news]=175484#5911JFP_Article4-tab1
13. Gregory M. Peterson. Generic Substitution of Antiepileptics: Need for a Balanced View. Accessed online Dec 2013. http://www.cnsspectrums.com/aspx/articledetail.aspx?articleid=3603
Yes, recent research has proven that most people allergic to eggs can safely receive trivalent inactivated influenza vaccine (Fluviral, Agriflu, Vaxigrip or FluZone for use in those 6 months and over and Influvac for use in those 18 years and over).
- People with mild reactions such as hives, or those who tolerate eggs in baked goods may be vaccinated in regular vaccination clinics.
- Those who have suffered from anaphylaxis with respiratory or cardiovascular symptoms should be vaccinated in a medical clinic, allergy office or hospital where appropriate expertise and equipment to manage respiratory or cardiovascular compromise is present. These individuals should always be kept under observation for 30 minutes.
- Although likely safe, there is not enough information to recommend live attenuated influenza vaccine (FluMist) for egg-allergic individuals at this time.
In the past, people with known allergic reactions to eggs (hives, swelling of the mouth and throat, difficulty in breathing, drop in blood pressure, or shock) were advised to avoid vaccines manufactured in egg, including influenza vaccines. However, a number of recent studies have found that the influenza vaccine does NOT cause any serious ill effects in most egg-allergic individuals. The benefits of receiving influenza vaccine therefore greatly exceed the small risk for people with egg allergy.
1) National Advisory Committee for Immunization (NACI) 2013–2014 flu season recommendations. Available at http://www.phac-aspc.gc.ca/publicat/ccdr-rmtc/13vol39/acs-dcc-4/index-eng.php. Accessed October 2013.
2) Centers for Disease Control and Prevention. Seasonal Influenza (Flu). Available at http://www.cdc.gov/flu/professionals/vaccination/vax-summary.htm
Prepared by Dorothy Sanderson BSP and Karen Jensen MSc, BSP
medSask, Your Medication Information Service
Oct 15, 2013.
Table: Change in Urine Colour and / or Appearance
|Urine Colour / Appearance||Foods||Drugs||Medical Conditions||Medical Advice|
|Cloudy white||Foods with a high purine content (E.g. anchovies, gravies, kidney, liver, sardines)||Not applicable||
- Urinary tract infection (UTI)- Kidney stones
Seek medical advice for confirmation and treatment, especially if symptoms are accompanied by pain or fever
|Blue or green||
- Asparagus- Brightly coloured food dyes
- Some dyes used for testing kidney and bladder function
- Blue diaper syndrome – an inherited condition that causes blue urine in babies- Urinary tract infections (UTI) caused by certain kinds of bacteria
Seek medical advice for confirmation and treatment if condition persists for longer than 24 hours, is accompanied by pain on urination or fever and if food or drugs cannot be ruled out.
- Carrot juice
- Vitamin C
- Dehydration- Liver or bile duct problems
Seek medical advice if accompanied by lethargy, headache, dry mouth, extreme thirst, rapid heartbeat or light coloured stools
|Red or pink||
- Blackberries- Rhubarb
- Senna and/or cascara containing laxatives
- Chronic lead or mercury poisoning- Presence of blood (hematuria)
|Seek medical advice if recent consumption of probable food causes cannot be ruled out|
- Fava beans
- Rhubarb- Aloe
- Senna and/or cascara containing laxatives
- Vitamin B complexes
- Some UTI’s- Breakdown of muscle tissue
|Seek medical advice if recent consumption of probable food causes cannot be ruled out or if accompanied by pain on urination, fever, yellow skin or pale stools|
|Foamy||Not applicable||Not applicable||
- Occasional foaminess is normal and may be influenced by the speed of passing urine or mild dehydration.
- Persistent foaminess may be a sign of protein in the urine (proteinuria) and may indicate a UTI or a kidney problem
|Seek medical advice if you have persistently foamy urine that becomes more noticeable over time. Testing may be necessary to determine the cause of the problem.|
2) http://www.uspharmacist.com/continuing_education/ceviewtest/lessonid/106254/ Urinalysis: A Guide for Pharmacists.
Produced by Jean Macpherson, BSP. Reviewed by Karen Jensen, MSc, BSP
medSask Drug Information Consultants
An electronic cigarette, or e-cigarette, is a battery-run device that mimics cigarette smoking by producing mist for inhalation with the feel, look, and in some countries, the flavor and nicotine content of tobacco smoke. The devices usually use heat to vaporize a propylene glycol or glycerin-based liquid solution into a mist, similar to the way a humidifier works. The mist can be inhaled and exhaled, creating a vapor cloud that looks like cigarette smoke. Because nothing is actually burning, smoking an e-cigarette is odorless, and it doesn’t produce any ash. (1, 2)
Most electronic cigarettes are about the shape and size of a ballpoint pen, although this varies depending on battery sizes. Many e-cigarettes are designed to look like actual cigarettes or cigars, or even pipes. Some models are reusable, with replaceable and refillable parts and some are disposable. (1, 2)
E-cigarettes containing nicotine are not approved for sale in Canada.(3,4) They are however, available in other countries including the United States and people may have tried them while travelling.(3) Products available in Canada may have the same brand names as nicotine-containing products from elsewhere but contain only aromas or flavorings without the nicotine. (2)
Health Canada advises Canadians not to purchase or use electronic smoking products containing nicotine, as these may pose health risks and have not been fully studied for safety, quality and efficacy by Health Canada.(4) E-cigarettes containing nicotine are advertised on the Internet but Canada Customs will seize orders containing these products if the department catches them.
Benefits versus risk
The possible benefits or adverse effects of electronic cigarette use are a subject of disagreement among different health organizations and researchers. While many people consider, and e-cigarette manufacturers claim, that these are safer than cigarettes, the effects have not been well studied. (1, 2)
E-cigarettes are advertised as an alternative to regular cigarettes, as they try to give the experience of smoking without the adverse health effects of tobacco smoke. Recent uncontrolled studies, reported that a certain number of smokers have quit smoking using electronic cigarettes.(1,2) This suggests electronic cigarettes may help people stop smoking..
Saskatchewan has one of the highest cigarette smoking prevalence rates in Canada. Prevalence of smoking among 15-19 year olds is higher in Saskatchewan than the national average.(5)
Unless smokers quit, up to half of them will die as a result of their smoking, most of them before their 70th birthday and after years of suffering a reduced quality of life. (3)
However, concerns have been raised that e-cigarettes may carry health risks of their own, and they could appeal to non-smokers, especially children, due to their novelty, flavorings, and claims of safety.(3,4) For stopping smoking, Health Canada has authorized the sale of several well-studied options, including over-the-counter nicotine replacement products (gum, lozenges, patches, etc.) and prescription medications (Zyban®, Champix®). (6)
The amount of nicotine in e-cigarette solutions varies by manufacturer, as there is no standard dose for each strength category (e.g., low, high). A consumer buying a nicotine-containing product marked as ‘high’ could receive a solution with a different concentration in nicotine from another product marked as ‘high’, depending on the manufacturer. The fatal dose of nicotine is estimated at 30–60 mg in adults and 10 mg in children. Studies have shown that some e-cigarette solutions contain nicotine doses potentially lethal in adults and children. For example, a 5 ml vial of a 20 mg/ml solution contains 100 mg of nicotine. (7)
Reports of unintentional poisoning in children from tobacco (cigarette butts) and smokeless tobacco (chewing tobacco or snuff) products suggest minor toxicity (e.g., vomiting, nausea, and increased heart rate) in most cases.(6) However, the amount of nicotine contained in the 5, 10 or 20 ml vials commonly uses in e-cigarettes, poses a much higher risk of severe toxicity or fatality in children if taken orally or absorbed through the skin. This is particularly concerning as e-cigarette nicotine solutions come in flavors attractive to children such as chocolate, cotton candy and bubble gum. (7)
Nicotine dependence can start to occur within weeks of occasional tobacco use, so even brief experimentation with nicotine-containing e-cigarettes could promote adolescents' interest in using other tobacco products. (8) Experts rank nicotine ahead of alcohol, cocaine and heroin with regard to the severity of dependence resulting from its use. Those who start to smoke at an early age are more likely to develop severe levels of nicotine addiction than those who start later, and they are at higher risk of adverse health effects in adult life. (5)
E-cigarettes may be helpful for people trying to stop smoking as they replace some of the habits associated with smoking cigarettes and could become a tool - if studied more extensively - in the fight against tobacco-related illness and death.(9)
Produced by Jean Macpherson, BSP. Reviewed by Karen Jensen, MSc, BSP
medSask Drug Information Consultants
- www.jasperandjasper.com/what-is-in-an-e-cig-pm-29.html. Accessed June 2013.
- http://jasperandjasper.ca/about-us-3. Accessed June 2013.
- O’Mara NB. Electronic Cigarettes and Hookah Pipes. Canadian Pharmacists’ Letter: PL Detail-Document. Pharmacist’s Letter/Prescriber’s Letter. May 2013.
- Health Canada. Health Canada Advises Canadians Not to Use Electronic Cigarettes. Available at http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/13373a-eng.php . Accessed June 2013.
- Gov’t Sask. Health effects of tobacco. Available at http://www.health.gov.sk.ca/health-effects-tobacco http://www.health.gov.sk.ca/health-effects-tobacco. Accessed Junes 2013.
- Health Canada. Drug Product Database. Available at http://webprod5.hc-sc.gc.ca/dpd-bdpp/index-eng.jsp . Accessed June 2013.
- Cameron JM., Howell DN, White JR et al. Variable and potentially fatal amounts of nicotine in e-cigarette nicotine solutions. Tobacco Control.2013.
- Pepper J, Reiter P, Annie D et al. Adolescent Males' Awareness of and Willingness to Try Electronic Cigarettes. Journal of Adolescent Health, Volume 52, Issue 2, February 2013, Pages 144–150.
- Caponnetto P, Russo C, Bruno CM et al. Electronic cigarette: A possible substitute for cigarette dependence, Monaldi Archives for Chest Disease - Pulmonary Series, 2013 (1) , pp. 12-19.
A concern with taking oral contraceptives or birth control pills is that they may slightly increase a woman’s chance of developing a venous thromboembolism (VTE). VTE is the development of a blood clot within the veins, usually in the legs or pelvis. The use of all oral contraceptives will increase the chances of developing VTE compared to a woman not taking an oral contraceptive.
Although the likelihood of developing VTE is rare it is still a serious condition. When identified and treated early, most VTE cases will get better without causing any long term problems. Sometimes the blood clot may break loose and travel to other parts of the body, such as the lungs, becoming a pulmonary embolism, which can be fatal. One out of 100 or 1% of pulmonary embolism cases are fatal (1 & 5).
The risk of blood clots is increased by many other factors including (but not limited to): immobility (not being active, sitting for prolonged periods of time), obesity, pregnancy, smoking, family history of blood clots, and blood clotting disorders. (1)
When considering oral contraceptives, you should be aware of the risks and benefits of these medications. For most women who choose to use oral contraceptives, the benefits usually outweigh the risk. They prevent pregnancy, reduce uterine cyst formation, decrease your chance of developing certain types of cancers such as ovarian and endometrial They can also help with menstrual symptoms and regularity. (1, 3 & 4) When discussing your oral contraceptive your doctor or pharmacist will ask questions about your health and family history to ensure the best oral contraceptive is prescribed for you.
To get a better understanding of the risk of VTE, The Society of Obstetricians and Gynecologist of Canada have posted a few comparative estimated rates for the development of VTE in woman (1 & 4):
Table 1: Rates of Venous Thromboembolism
Not taking oral contraceptives
0.04 – 0.05%
Taking oral contraceptives
0.08 – 0.1%
Up to 29/10,000
After giving birth (first few weeks)
Up to 300-400/10000
3 – 4%
The death rate from oral contraceptive use is 1/100 000 or 0.001% when taking into considerations the values above (1).
Yaz® and Yazmin® are combination oral contraceptives. This means that they contain a combination of two hormones estrogen and progesterone. The synthetic estrogen is called ethinyl estradiol and the synthetic form of progestin is termed drospirenone. (2)
There has been some controversy over whether Yaz ® and Yasmin® increases the chances of developing VTE more than other oral contraceptives. The evidence associated with these claims or with the comparison of risk between oral contraceptives is conflicting. (1, 4, & 5) Some studies suggest there is a slight increase in risk of VTE when using the newer generation progestin; however, some studies have also suggested that there is no significant difference between them. (1, 4, & 5) Because of the conflicting evidence, we cannot say that Yaz ® and Yasmin® do or do not have higher VTE risk associated with them in regards to other oral contraceptives.
- If you are currently taking Yaz ® and Yasmin® then there is no need to switch or stop. The risk of developing a VTE when using oral contraceptives is highest in the first few months, so if you have been on it long term, your risk is normal.
- If you are starting an oral contraceptive for the first time or switching, consider using an oral contraceptive other than Yaz ® and Yasmin®, especially if you are concerned or have other risk factors for VTE.
- With this being said, Yaz ® and Yasmin® may be appropriate choices for woman with certain conditions, such as acne or excess body hair.
If you are taking an
oral contraceptive it is good to know the signs and symptoms of VTE (Table 2).
If you experience any of these see a doctor as soon as possible.
Table 2: Signs and symptoms of VTE
In the LEG
In the LUNG
Pain in the leg or calf
Sharp chest pain
Increased warmth in leg
Shortness of breath
Swelling in the calf, ankle, or foot
Coughing (possibly coughing up blood)
Red, purple, or blue discoloration in the leg
Redness of skin
Produced by Joanne Fontaine, Pharmacy student, medSask
Reviewed by Karen Jensen MSC, BSP, Carmen Bell BSP; Terry Damm BSP
1. The Society of Obstetricians and Gynaecologists of Canada. Position Statement: Hormonal Contraception and Risk of Venous Thromboembolism (VTE). Available at http://sogc.org/media_updates/position-statement-hormonal-contraception-and-risk-of-venous-thromboembolism-vte/. Accessed June, 2013
2. Lexicomp. Yaz . Available at www.lexi-com by subscription. Accessed June, 2013
3. Rx files. YASMIN: Hormonal Contraception- Supplement Tables. Available at http://www.rxfiles.ca/rxfiles/uploads/documents/members/CHT-OCs-Color.pdf. Accessed June, 2013
4. Rx files. YASMIN: Safety Considerations related to Venous Thromboembolism (VTE). Available at http://www.rxfiles.ca/rxfiles/uploads/documents/Yaz-Yasmin-Q-A.pdf. Accessed June, 2013
5. Food and Drug Administration. Updated External Questions and Answers – Ongoing safety review of birth control pills containing drospirenone and a possible increased risk of blood clots. Available at http://www.fda.gov/Drugs/DrugSafety/ucm299348.htm. Accessed June, 2013
6. Patient Health International. Venous Thromboembolism. Available at http://www.patienthealthinternational.com/venous-thromboembolism/facts-and-figures/symptoms?itemId=1620499&nav=yes. Accessed June, 2013
There has been a lot of media buzz for omega supplements, and many people have started taking them for various purposes; but do they actually help any conditions, and which supplements are best?
Navigating the omega supplement aisle is a daunting experience. There are omega-3, omega-6, omega 3-6-9, alpha-linolenic acid, krill oil, salmon oil, flaxseed oil and many more supplements to confuse a shopper. Many of the products available are either marketing gimmicks that have no value, or have not been shown to help for most conditions.
- Dietary omega-3 from two to three servings of fatty fish (salmon, mackerel, tuna, sardines, or white fish) per week continues to be recommended for maintenance of good health (1)
- Fish oil omega-3 supplements may not be as useful for heart health as once suspected
- Fish oil omega-3 supplements are very safe when taken in doses under 3g per day. Higher doses can lead to problems and should not be taken without consulting your doctor or pharmacist.
- Omega-6 and omega-9 are heart healthy fats; however, most people have too much in their diet and excess supplementation can lead to harm.
The following is a review of the safety and effectiveness of various omega fatty-acid supplements.
1) Omega-3 supplements
Omega-3 supplements have the largest amount of research behind them. They have been promoted for preventing heart disease and stroke, and may also have a role in treating rheumatoid arthritis, mental health problems and dementia (2,3). However, there is limited or inconclusive evidence that omega-3 supplements actually help these conditions. Until more reliable information becomes available, omega-3 supplements cannot be recommended for these conditions.
The types of omega-3 fatty acids with the most research in various health conditions are called EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid). The other types of omega-3 supplements, such as flaxseed oil or other plant sources, do not have as much research behind them.
Fish oil, which provides EPA and DHA, has been used to help prevent strokes or heart attacks, and to also lower triglycerides. Original research showed a modest improvement in cardiovascular health and a reduction in heart attacks and stroke, especially in a person who had already had a heart attack or stroke (2).
However, a new body of quality research suggests fish oil supplements do not improve heart health or reduce the risk of heart attack or stroke (4,5). In contrast, one study found higher dietary omega-3 intake from fatty-fish (salmon, mackerel, tuna, sardines, or white fish) reduced the risk of stroke (6).
Fish oils also have been investigated for their use in improving mental health, dementia, and rheumatoid arthritis; the evidence is inconclusive and requires further research (7).
Fish oil supplements are not a substitute for a healthy diet, which incorporates two or three servings of fish per week, since supplements may not have the same heart health benefits as omega-3 obtained through the diet.
If you do choose to take a fish oil supplement, there are some potential side effects and safety issues. Fish oil supplements most commonly cause a fishy aftertaste or "fishy burp." They can also cause heartburn, nausea, diarrhea or rash, but they are usually well tolerated. Taking supplements with meals or freezing them seems to help decrease these side effects for some patients. Doses higher than 3g per day can lead to more harm (such as an increase in LDL cholesterol and an increased risk of internal bleeds if you’re also taking an anti-coagulant medication like warfarin) than benefits, and should not be taken without consulting your doctor or pharmacist (7).
Krill Oil also provides EPA and DHA, but in much lower amounts than other fish oil supplements, and there is also no data showing cardiovascular benefits. If you want to try an omega-3 supplement, regular fish oil supplements should be tried first. If there are too many side-effects, then a krill oil supplement can be tried. Most brands of Krill oil also contain Vitamin A, D and E, so care must be taken to be sure you are not taking more than the safe daily amounts of these vitamins (2).
Alpha-linolenic acid (ALA) is another type of omega-3 supplement and is found in flaxseed oil. There is very limited evidence ALA supplementation is helpful in cardiovascular disease, although increasing dietary intake of ALA may be useful for heart health (1). ALA does not replace the EPA and DHA you should get in your diet (2,7).
Omega-3 supplements are often marketed as a miracle pill, but they do not appear to have the benefits they were once thought to have. Dietary omega-3 from fatty fish continues to be recommended to maintain general health. If you do choose to take an omega-3 supplement, only omega-3 found in fish oil products might be beneficial, and they are safe supplements to take at doses of less than 3g per day.
2) Omega-6 supplements
fatty acids come from vegetable oils, soy and nuts. Omega-6 is a heart healthy fat, but in the typical
western diet, most individuals already consume too much, so supplementing more
is not necessary; omega-6 in excess amounts found in supplements can be harmful,
leading to an increase inflammation, constriction of blood vessels and a
possible negative impact on heart health (2).
3) Omega-9 supplements
Omega-9 supplements have not been studied as extensively as Omega-3. The most common source of Omega-9 is olive oil. The only available evidence suggests if olive oil replaces other fats and oils in the diet, it can have a benefit to cholesterol levels and overall cardiovascular health. If you are considering using olive oil in your diet, ensure it replaces other oils, rather than adding to other oils (2,7).
1) Health Canada Food Guide. Accessed online, 2013 April 10.
2) PL Detail-Document, Omega-3 Fatty Acids. Pharmacist’s Letter/Prescriber’s Letter. August 2012.
3) Heather Hutchins, MS, RD. Symposium
Highlights -- Omega-3 Fatty Acids: Recommendations for Therapeutics and
Prevention. Accessed Online, 2013 April
4) Kwak SM, Myung SK, Lee YJ, Seo HG. Efficacy of omega-3 fatty acid supplements (eicosapentaenoic acid and docosahexaenoic acid) in the secondary prevention of cardiovascular disease: a meta-analysis of randomized, double-blind, placebo-controlled trials. Arch Intern Med. 2012 May 14;172(9):686-94. Accessed online at: http://www.ncbi.nlm.nih.gov/pubmed/22493407]
5) Evangelos C. Rizos, MD, PhD; Evangelia E. Ntzani, et al. Association Between Omega-3 Fatty Acid Supplementation and Risk of Major Cardiovascular Disease EventsA Systematic Review and Meta-analysis. JAMA. 2012;308(10):1024-1033. Accessed online at: [http://jama.jamanetwork.com/article.aspx?articleid=1357266]
6) Association between fish consumption, long chain omega 3 fatty acids, and risk of cerebrovascular disease: systematic review and meta-analysis. BMJ 2012;345:e6698. Accessed online at: [http://www.bmj.com/content/345/bmj.e6698]
7) Natural Medicines Comprehensive Database. Accessed Online, 2013 April 10.
The term hepatitis literally means “inflammation of the liver”. This can be caused by excessive alcohol use and by some toxic substances, but it is most commonly caused by a virus, Hepatitis A, B or C. The following table summarizes the differences between the different types of hepatitis infection.
|Hepatitis A||Hepatitis B||Hepatitis C|
Prepared by Jean Macpherson BSP. Reviewed by Karen Jensen MSc, BSP.
medSask: Your Medication Iinformation Service
June 5, 2013
- 1. MedlinePlus. Hepatitis A. Available at http://www.nlm.nih.gov/medlineplus/hepatitisa.html. Accessed May, 2013
- 2. MedlinePlus. Hepatitis B. Available at http://www.nlm.nih.gov/medlineplus/hepatitisa.html. Accessed May 2013.
- 3. MedlinePlus. Hepatitis C. Available at http://www.nlm.nih.gov/medlineplus/hepatitisa.html. Accessed May 2013.
- 4. Cheney, Catherine P. Overview of hepatitis A virus infection in adults. In: UpToDate, Hirsch, MS (Ed), UpToDate, Waltham, MA, 2012.
- 5. Sanjiv Chopra. Clinical manifestations and natural history of hepatitis C virus infection. . In: UpToDate, Adrian M Di Bisceglie (Ed), UpToDate, Waltham, MA, 2012.
- 6. Crespi, Judy. The A, B, Cs (+ D + E) of hepatitis. Review - American Pharmacists Association Continuing Pharmacy Education. Pharmacy Today 2012; May: 75 – 84. Available at pharmacists.com. Accessed May 2013.
There is unclear or conflicting scientific evidence for the claim that Garcinia cambogia is useful for weight loss. Much of the positive evidence comes from laboratory and animal studies. Reviews of the studies done with people conclude that Garcinia cambogia
- Does not decrease weight or burn fat in obese people
- Might cause people to eat less by making them feel full, but more studies are needed to prove this helps people lose weight.
Garcinia cambogia is an extremely small, purple fruit that is naturally found in India and Southeast Asia. It is used to flavor food in Thai and Indian cooking. The rind of the fruit is rich in a substance called hydroxycitric acid (HCA). It has been proposed that HCA helps the body burn carbohydrates and fat.
It is considered to be safe when used in doses of up to 2800 mg daily for 12 weeks or less. There is no reliable information on its safety in long-term use.
Side effects Garcinia cambogia may cause include nausea, upset stomach, and headache.
People should use Garcinia cambogia cautiously if they:
- Have diabetes because it can affect blood sugar levels.
- Take a ‘statin’ drug, for example, atorvastatin (Lipitor, generics) or rosuvastatin (Crestor) to lower cholesterol as it may increase the risk of having an adverse reaction involving the breakdown of muscle tissue.
- Have Alzheimer’s disease or other dementia disorders as it may increase production of a chemical in the brain which affects these conditions.
Prepared by Jean Macpherson, BSP. Reviewed by Karen Jensen BSP, MSc and Carmen Bell, BSP.
1) Garcinia cambogia monograph. Natural Medicines Comprehensive Database. Available online by subscription. Accessed May 14, 2013
2) Garcinia (Garcinia cambogia), Hydroxycitric acid Natural Standard Professional Monograph, Copyright © 2013 (www.naturalstandard.com). Accessed May 14, 2013.
3) Health Canada. Licensed Natural Health Products Database. Available at http://webprod3.hc-sc.gc.ca/lnhpd-bdpsnh/index-eng.jsp. Accessed May 20, 2013.
4) Márqueza F, Babioa N, et al. Evaluation of the Safety and Efficacy of Hydroxycitric Acid or Garcinia cambogia Extracts in Humans. Critical Reviews in Food Science and Nutrition 2012;52: 585-594.
Q. Do vitamin supplements help prevent or reduce age-related macular degeneration (AMD)?
- There are not any miracle supplements to help cure or prevent AMD.
- No supplements have been proven to prevent AMD.
- The Vitalux-AREDS® formula may slow the progression of intermediate to advanced dry AMD, but does not prevent AMD.
- Vitamins for eye health can potentially be harmful and should not be started without consulting your optometrist, doctor or pharmacist.
- Improving your diet by increasing fatty fish and vegetable intake may help your eye health.
Many vitamin, mineral and herbal products are on the market promoting healthier eyes, enhanced vision, or even treating age-related macular degeneration (AMD).
But is there any truth behind these products?
AMD is a major cause of blindness in adults, leading many people to do whatever they can to prevent the condition. There are two types of AMD—wet and dry—which influences what supplements are effective.
Dry AMD is more common than wet AMD. Dry AMD causes vision loss slowly and gradually, and progresses in three-stages: early, intermediate and advanced. In contrast, wet AMD causes rapid distortion and severe loss of vision. Dry AMD can progress into wet AMD. (2,3)
There is some evidence that supplements can help slow the progression of dry AMD at certain stages; wet AMD cannot be treated with supplements and requires more specialised treatment. (2)
The following is a review of the safety and effectiveness of different supplements used to treat dry AMD:
1) Omega-3 fatty acids
A few studies have found that dietary omega-3 fatty acids (found in fatty fish like salmon, mackerel, tuna, sardines, or white fish) helped protect against developing the early stages of AMD and progressing to more advanced stages. However, no studies have been done to show omega-3 supplements help with AMD. Consider increasing your intake of fatty fish to two servings per week to help with eye health, but supplements are not yet proven (1).
Omega-3 supplements are very safe when taken in normal amounts of under 2-3 grams of fish oil per day. Some people experience a fishy aftertaste or ‘fish burp’ while on the supplements. Others also experience nausea, diarrhea or heartburn, but is generally very well tolerated. People taking drugs that affect blood clotting, like warfarin, should not take over 3 grams of fish oils per day, as this can increase your risk of bleeding.
Lutein, by itself, has been marketed for eye-health. Few studies have been done with dietary and supplementary lutein. Dietary lutein was associated with a lower chance of developing wet AMD (2), but a lutein supplement versus a combination supplement or placebo found no improvement (1). Lutein is found in green, leafy vegetables such as kale, spinach, swiss chard and romaine lettuce. Try increasing your intake of these vegetables to get the protective benefits of lutein, though there is no proof it will prevent the development of early AMD. A lutein supplement may not be as effective.
Lutein has an excellent safety profile; no adverse effects have been reported with normal doses of 10mg / day. (5)
3) Anti-oxidants (beta-carotene, vitamin C, vitamin E and zinc)
The above anti-oxidants are found in products such as Vitalux-AREDS® and Ocuvite®. The Vitalux-AREDS® has been proven to help slow the progression from intermediate to advanced dry AMD, but does not help prevent it from occurring. If you have dry AMD, the Vitalux formula may benefit you. (1)
Eye vitamin formulations should not be started without consulting your optometrist, doctor or pharmacist as they can be harmful to certain people. It has been found that vitamin supplement with high doses of anti-oxidants (such as found in Vitalux® or Ocuvite®) may cause more harm than benefit in some patients (4). One study found patients taking high doses of anti-oxidants had a slightly increased chance of death from all causes (6). This risk seems limited to supplement anti-oxidants; dietary anti-oxidants have no known risks. Until more is known about the benefits or drawbacks to anti-oxidants in supplements, they should only be used where they might have a benefit—for those with intermediate or advanced AMD.
Prepared by Terry Damm, BSP
Reviewed by: Karen Jensen, BSP and Carmen Bell, BSP
medSask Medication Information Consultants
1) Age-related macular degeneration: an update. Pharmacist's Letter/Prescriber's Letter 2009;25(7):250719.
2) UpToDate, Age-related macular degeneration: Treatment and prevention
3) National Eye Institute. http://www.nei.nih.gov/health/maculardegen/armd_facts.asp
R. Kolber, Tony Nickonchuk. Tools of Practice, Vitamins for age-related macular degeneration (AMD) demonstrates
5) Natural Medicines Comprehensive database
6) Bjelakovic G, Nikolova D. Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases. Cochrane Database Syst Rev. 2008 Apr 16;(2):
If breastfeeding is not an option, use a store-bought infant formula for the first 9 to 12 months :
- First choice - use an iron-fortified cow milk-based formula
- Diagnosed allergy to cow milk - use a hydrolyzed protein formula (cow milk protein which has been partially broken down)
- Galactosemia (an inherited disorder in which human and/or cow milk is not properly digested) – use a soy-based formula
- Animal products prohibited for cultural or religious reasons – use a soy-based formula
Exclusive breastfeeding for baby’s first six months is the ideal method of feeding an infant, but this may not be possible for personal, medical, or social reasons. The commercial infant formula chosen must be appropriate for the infant, and prepared and stored safely to reduce the risk of illness from bacterial growth.
Infant formula nutritional composition and additives are set by the Canadian Food and Drug Regulations. Health Canada requires the manufacturer to submit details of the formulation, ingredients, processing, packaging, and labeling for review. Manufacturers must also submit evidence that the formula is nutritionally adequate to support growth and development.
Cow milk-based regular formulas
These formulas are made from cow milk which has been modified to make it similar to human milk. A store-bought infant formula contains all the nutrients that healthy babies need. Several different brands are available. They may contain a single milk protein or a combination of whole milk protein, casein or whey. There is no evidence that one brand is better than another.
Protein hydrolysate formulas
The only products recommended by the Canadian Pediatric Society for a baby with proven cow milk protein allergy are hydrolyzed protein formulas e.g. Nutramigen, Alimentum. Babies allergic to cow milk are quite likely to have a similar reaction to soy-based formulas. For babies who are highly allergic to cow milk proteins, an amino acid-based infant formula may be recommended.
Soy-based infant formula is indicated ONLY for infants who have galactosemia, a congenital lactase deficiency or who cannot consume cow milk-based products for cultural or religious reasons. Soy formula is shown to provide normal nutrition and support normal growth in babies’ first year. The routine use of soy-based formula has not been proven to prevent or manage infant colic, spitting up, fussiness or prolonged crying and does not prevent allergic reactions in healthy or high-risk infants. Babies allergic to cow milk are quite likely to have a similar reaction to soy-based formulas.Not recommended for infants less than 12 months:
- Cow milk (unaltered) and other animal milks, including goat milk, are not appropriate alternatives to breastmilk for babies. They are low in iron, essential fatty acids and other necessary nutrients, contain a less-digestible form of protein and have too many components which could harm infants’ kidneys.
- Soy, rice or other plant-based beverages, even when they are fortified, are not appropriate as a breastmilk substitute because they are nutritionally incomplete. Consumption of these beverages by babies may result in failure to thrive.
- Lactose-free cow milk formula still contains a small amount of lactose and should not be used for infants with a confirmed cow milk protein allergy or with galactosemia. (2)
infant formulas are intended for use only under medical supervision. They
include formulas for the dietary management of some medical and digestive
conditions and for preterm infants. These products should not be used for
healthy term infants and are not generally available at the retail stores.
Prepared by Jean
Macpherson, BSP. Reviewed by Karen Jensen, MSc, BSP.
medSask Drug Information Consultants
1) Baby Centre Canada. Find a formula that’s right for you. Available at http://www.babycenter.ca/a1050266/find-a-formula-thats-right-for-you . Accessed Feb. 2013.
2) Canadian Paediatric Society. Caring for Kids. Available at www.caringforkids.cps.ca. Accessed Feb. 2013.
3) Health Canada. Recommendations on the use of breastmilk substitutes. Available at http://www.hc-sc.gc.ca/fn-an/nutrition/infant-nourisson/recom/index-eng.php#a11. Accessed Feb. 2013.
4) Mayo Clinic. Infant and toddler health. Infant formula: Your questions answered. Available at http://www.mayoclinic.com/health/infant-formula/PR00058. Accessed Mar. 2013.
5) National Institute Environmental Health Sciences. Final CERHR expert panel report on soy infant formula. Available at http://ntp.niehs.nih.gov/ntp/ohat/genistein-soy/SoyFormulaUpdt/FinalEPReport_508.pdf. Accessed Feb. 2013.
Health Canada and the US Food and Drug Administration have added label warnings to all statin medications that they can increase blood sugar levels and increase the risk of diabetes. Understandably, this has many patients concerned if they should discontinue their statin. Statins are drugs used to treat high cholesterol and/or people at high risk of cardiovascular (heart) disease; some diabetics have an increased risk of cardiovascular disease compared to non-diabetics. Statins include: atorvastatin (Lipitor®), fluvastatin (Lescol®), lovastatin (Mevacor®), pravastatin (Pravachol®), rosuvastatin (Crestor®), and simvastatin (Zocor®).
- Statins reduce the risk of heart attack and strokes. These benefits have been consistently reported in all studies and outweigh the possible harm of higher blood sugar levels and being diagnosed as diabetic
- Worsening blood sugar control (and the risk of becoming diabetic) is more likely with higher doses of statins, or more potent statins (atorvastatin, rosuvastatin or simvastatin)higher doses of statins, or stronger statins (atorvastatin, rosuvastatin or simvastatin).
- A diabetic patient has an even greater life-saving benefit from statins, compared to a non-diabetic patient, despite the potential for slightly increasing blood sugar levels
Reviews of the medical literature indicate diabetes may occur more frequentlylence of diabetes in people who have taken statins. One report showed a 9% increase (2); another showed 13% (3); and lastly, one showed up to 27% (4). These numbers can be alarming, but interpreting these results in a balanced way is important.
The above values are relative increases and translate into one extra case of diabetes per 1000 patients in a year; however, statins prevent 9 cardiovascular events (heart attack, stroke) per 1000 patients in a year (1). This means that when statins are used in the right patients, they prevent 9 times as many potentially life-threatening conditions as compared to causing diabetes.
So what should you do?
If you have a high risk of developing cardiovascular disease, being on a statin is proven to have significant life-saving effects, especially if you also have diabetes (5). A high risk of cardiovascular disease would mean (6):
- All people with a history of heart-attack or stroke
- Diabetics older than 45 if male, or 50 if female, with one other of the risk factors listed below.
- People with 2 or 3 of the risk factors listed below.
- Risk factors for cardiovascular disease
- High blood pressure (greater than 140/90)
- Low HDL cholesterol
- High LDL cholesterol
- Overweight (waist circumference: male >40 inches (102 cm), female >35 inches (88 m), or BMI >25 kg/m2)
- Family history of early heart disease (male <55, female <65)
Your doctor or pharmacist can also perform something called a “Framingham Risk Assessment,” which helps determine your risk of cardiovascular disease and if a statin is the right treatment for you. If you do have a high risk for cardiovascular disease, remaining on the statin is important. If your risk is low, you and your doctor can consider discontinuing the statin and trying life-style changes instead (exercise, weight loss) to improve your cholesterol.
by Terry Damm BSP. Reviewed by Carmen Bell, BSP and Karen Jensen MSc, BSP
1. PL Detail-Document, Update on Statin Risks. Pharmacist’s Letter/Prescriber’s Letter. April 2012
2. Sattar N, Preiss D, Murray HM, et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials. Lancet 2010;375:735-42.
3. Sabatine MS, Wiviott SD, Morrow DA, et al. High-dose atorvastatin associated with worse glycemic control: a PROVE-IT TIMI 22 substudy. Circulation 2004;110(Suppl I):S834.
4. Rajpathak SN, Kumbhani DJ, Crandall J, et al. Statin therapy and risk of developing type 2 diabetes: a meta-analysis. Diabetes Care 2009;32:1924-9.
5. UpToDate, Statins: Actions, side effects, and administration
6. Jacques Genest MD1, Ruth McPherson, et al. 2009 Canadian Cardiovascular Society/Canadian
guidelines for the diagnosis and treatment of dyslipidemia and prevention of cardiovascular disease in the adult – 2009 recommendations.
• Normal blood pressure can range from 90/60 to 140/90. Lower than 90/60 is considered low blood pressure
• Low blood pressure is only a cause for concern if the person experiences symptoms as well: dizziness, unusual fatigue, weakness, headache, chest-pain or fainting upon quickly rising. A doctor should be seen as soon as possible if these symptoms are present.
We always hear about the dangers and health risks of high blood pressure, but what about blood pressure that is too low?
Normal blood pressure can greatly range depending on a person’s age and activity level—anywhere from 90/60 to 140/90. Blood pressure less than 90/60 is considered ‘hypotension’, the opposite of ‘hypertension’. (2)
Generally, low blood pressure is not a concern unless a person is experiencing some symptoms along with their low blood pressure. This indicates that their blood pressure is too low for their body. Symptoms of low blood pressure include: (1)
• Dizziness, light-headedness
• Fainting upon quickly rising
• Unusual fatigue
• Chest pain
If you experience any of those symptoms, and your blood pressure is lower than normal, you should make an appointment with your doctor as soon as possible. Low blood pressure does not require an emergency room visit, unless symptoms are very severe, such as loss of consciousness or chest pain that does not resolve. (2)
If you have low blood pressure, but feel fine, medical attention is not necessary. You should still mention it to your doctor so he/she can monitor you.
There are many causes of low blood pressure. The most common causes are dehydration and medications, such as diuretics, beta-blockers, and certain types of anti-depressants. (2)
If you are on medications and are concerned about low blood pressure, ask your pharmacist if certain medications could be contributing to your low blood pressure.
1) UpToDate, Mechanisms, causes, and evaluation of orthostatic and postprandial hypotension.
Accessed Dec 2012.
2) MayoClinic, http://www.mayoclinic.com/health/low-blood-pressure/DS00590. Accessed Dec 2012.
Q. I have just started a statin type medication for cholesterol. I have heard that I must now avoid grapefruit products. Is this true?
There are several statins” used to reduce cholesterol. Not all are at risk of interacting with grapefruit. Simvastatin (Zocor and generics brands), lovastatin (Mevacor and generic brands) and atorvastatin (Lipitor and generic brands) are at high risk for interaction which in rare cases can result in severe muscle and kidney damage. When taken at the same time, large amounts of grapefruit juice markedly to very markedly increase lovastatin and simvastatin levels in the body, and moderately increase atorvastatin levels. Smaller amounts of grapefruit juice and separating administration by twelve hours decrease but don’t completely prevent this effect.
The statin medications that don’t interact with grapefruit are pravastatin (Pravachol and generic brands), rosuvastatin (Crestor and generic brands) and fluvastatin (Lescol and generic brands).
What causes the interaction?
Grapefruit contains chemicals (furanocoumarins) which interfere with an enzyme (CYP3A) that breaks down (metabolizes) certain medications in your digestive system. As a result a larger amount of medication is absorbed into your body resulting in a potentially harmful dose. Because the chemicals which cause this effect are natural to grapefruit all forms of the fruit (juice, whole fruit) have the potential to reduce the activity of the enzyme. Seville oranges (often used in marmalades), limes and pomelos also produce this interaction. Sweet oranges such as Navel or Valencia do not contain furanocoumarins and therefore do not produce this interaction.
Usually grapefruit has been consumed every day for 3 to 5 days before an interaction has occurred. Occasionally however, a single serving of grapefruit juice or a whole grapefruit has resulted in an interaction, such as has occurred with the blood pressure lowering medication felodipine. After a single serving of grapefruit the drug concentration of felodipine increased to three times normal. This resulted in dangerously low blood pressure in some people.
Interactions with other medications
Serious adverse events that have been reported due to grapefruit-drug interactions with other medications include heart rhythm problems, heart blockage, kidney failure and blood clots.
The significance of any particular interaction depends on the seriousness of the dose related drug toxicity and the extent to which the drug concentration increases. You may be able to have a grapefruit occasionally or be switched to a medication that has the same benefit to you but does not interact with grapefruit. Check with your pharmacist or phone the Saskatchewan Drug Information Service at 1-800-665-3784 to see if you must avoid grapefruit and its juice with your medication.
Written by: Lisa Hupka, BSP. Reviewed by: Karen Jensen MSc, BSP
1. http://www.pharmacytimes.com/news/ Grapefruit-Can-Dramactically Increase Medication Potency. (accessed Dec.2012 )
2. http://www.mayoclinic.com/health/food-and-nutrition/AN00413 Katherine Zeratsky,R.D.,L.D. Consumer Health. (accesssed Dec.2012)
3. http://www.cmaj.ca/content/early/2012/11/26/cmj.120951 Grapefruit-medication interactions: Forbidden fruit or avoidable consequences? David G.Bailey, George Dresser, and J. Malcolm O. Arnold. November, 26, 2012. (accessed Dec.2012)
4. http://www.medicinescomplete.com/mc/stockley/current/interactions.htm?q=grapefruit&searchButton=Search (accessed Jan. 2013)
5. http://www.canadianhealthcarenetwork.ca/ Grapefruit can interfere with many drugs to cause severe effects or death: study. (accessed Dec.2012)
Avoid drinking any alcohol if you are taking:
• Ketoconazole: Alcohol consumption might cause flushing, headache, and nausea. Avoid alcohol and alcohol-containing drugs for at least 24 to 40 hours after the last dose.
• Metronidazole (Flagyl): Alcohol consumption might cause flushing, headache, and nausea. Avoid alcohol or alcohol-containing drugs while taking metronidazole and for at least 1 day after the last dose.
• Erythromycin (Eryc, Novo-rythro, Erythro-s): These may increase the amount of alcohol absorbed, so be aware that alcohol may have a stronger effect than you are used to.
If your alcohol consumption is greater than the occasional social drink or if you are not certain about taking your medicine correctly you should always check with your pharmacist.
Prepared by Jean Macpherson, BSP, Drug information consultant. Reviewed by Karen Jensen MSc, BSP.
1) Alcohol-related drug interactions. Pharmacist's Letter/Prescriber's Letter 2008;24(1):240106.
2) Lexicomp Online Interactions
3) Stockley’s Drug Interactions , 9th edition. Online version available at http://www.medicinescomplete.com by subscription.
Fever may be associated with unpleasant symptoms such as headache, drowsiness, lack of energy, chills, shaking, aches and pains.(1,2) Non-drug measures to treat fever symptoms include cooling by removing extra clothing or bedding, increasing fluids, and encouraging rest.(2) Acetaminophen or ibuprofen can be used if your child is very uncomfortable. Recommended doses (1,2) are:
• Acetaminophen 10 to 15 mg/kg (2.2 lbs) every 4 to 6 hours as needed (Maximum five doses/24 hrs)
• Ibuprofen 5 to 10 mg/kg (2.2 lbs) every 6 to– 8 hours as needed (Maximum four doses/24 hrs)
If you are unsure about calculating the dose for your child, ask your pharmacist or call the Drug Information Service. Always use the measuring device provided with the product when giving the medicine to your child. Giving doses at regular intervals may provide better symptom relief than occasional doses.(1,2)
There is no evidence that taking acetaminophen and ibuprofen together or alternating between one and the other is any better at reducing symptoms than taking either medicine alone. Mixing acetaminophen and ibuprofen dosing increases the chance of giving too high a dose of either medicine and is not recommended. (3,4)
Contact your doctor if:
• Fever is more than 40.5 deg C
• Child seems very sick
• Child has stiff neck,
• A seizure occurs
• Child is confused or delirious
• Child is crying without stopping
• Fever lasts for longer than 3 days
Prepared by Karen Jensen MSc, BSP
Saskatchewan Drug Information Service
Tel: 306-966-6378 (Saskatoon); 1-800-665-3784 (Saskatchewan)
1. Shevchuk Y. Chapter 9: Fever. In Patient SelfCare, 2nd Ed. CPhA, Ottawa, 2010: pg 80-93.
2. Ward M. Pathophysiology and management of fever in infants and children in UpToDate online. Available at www.uptodate.com by subscription. Updated Oct. 1, 2012. Accessed December, 2012.
3. Purssell E. Systematic review of studies comparing combined treatment with paracetamol and ibuprofen, with either drug alone. Arch Dis Child. 2011 Dec;96(12):1175-9.
4. Kramer L, Richards PA, Thompson A et al. Alternating antipyretics: antipyretic efficacy of acetaminophen versus acetaminophen alternated with ibuprofen in children. Clin Pediatr (Phila). 2008;47(9):907.
Pain control: For children older than 6 months with mild symptoms, ibuprofen or acetaminophen can be given for ear pain. Warmed oils placed in ear canal with a dropper and / or applying heat or cold to the ear may provide temporary relief. There is little evidence that natural or homeopathic remedies are of any benefit. If there is no improvement in symptoms in 48 to 72 hours, contacting the doctor is recommended.(1,2,3)
Decongestants / antihistamines are NOT recommended: Nasal sprays and oral decongestants alone or in combination with an antihistamine have not been shown to be effective in helping symptoms or preventing complications of ear infections.
Antihistamines such as diphenhydramine (Benadryl, generics; Chlortripolon, generics) may actually increase the length of time that fluid remains in the middle ear.(1,3)
Effusion (fluid in middle ear): It is common for fluid to remain in the middle ear for up to 3 months after an ear infection. For most children, this condition will go away without any treatment. This most common symptom is hearing loss. If hearing problems last for longer than 3 month, contact your doctor.(4)
Measures that help prevent childhood ear infections(1, 2):
• Ensuring your child gets a flu shot every year and that all other vaccinations are up to date.
• Children who are breastfed for at least 3 months have fewer ear infections in the first year.
• Avoid having your child exposed to tobacco smoke
• Children who do not go to daycare are less likely to get ear infections.
Prepared by Jean Macpherson BSP and Karen Jensen BSP, MSc. Reviewed by Dr. Yvonne Shevchuk, BSP, Pharm D.
1) Vayalumka, J.V., Infectious Diseases: Acute Otitis Media in Childhood. In: Repchinsky Carol, editor. e-Therapeutics+ [Internet]. Ottawa (ON): Canadian Pharmacists Association; c2012 [updated Oct 2011; cited 2012 Nov. 14]. Available from: http://www.e-therapeutics.ca. Also available in paper copy from the publisher.
2) Treatment of acute otitis media. Pharmacist's Letter/Prescriber's Letter 2009;25(11):251119.
3) Klein J, Pelton S. Otitis media in children: Treatment. UpToDate online database. Updated Nov 29, 2012. Available by subscription at www.uptodate.com. Accessed December 2012.
4) Klein J, Pelton S. Otitis media with effusion (serous otitis media) in children. UpToDate online database. Updated Jan 12, 2012. Available by subscription at www.uptodate.com. Accessed December 2012.
If it is difficult for you to schedule or remember to take thyroid hormone doses on an empty stomach, talk to your pharmacist or doctor. Taking the medicine with a meal is better than missing doses.(5) Another option sometimes used is taking a larger dose once weekly.(6) The most important thing is to be consistent – always take thyroid hormone medicine about the same time each day.(1) This way your dose can be adjusted to ensure that your thyroid levels stay in the normal range.
Prepared by Jean Macpherson, BSP and Karen Jensen, MSc, BSP
1. Canadian Pharmacists’ Letter: PL Detail-Document #281112, Helping patients take levothyroxine. 2012; 28, No. 11.
2. Bach-Huynh T.G., Nayak B., Loh J., et al: Timing of levothyroxine administration affects serum thyrotropin concentration. J Clin Endocrinol Metab 2009;94:3905-3912.
3. Bolk N., Visser T.J., Nijman J., et al: Effects of evening vs morning levothyroxine intake: a randomized double-blind crossover trial. Arch Intern Med 2010;170:1996-2003.
4. Vanderpump M. Pharmacotherapy: hypothyroidism-should levothyroxine be taken at bedtime?. Nat Rev Endocrinol 2011;7:195-196.
5. Zeitler P, Solberg,P. Food and Levothyroxine Administration in Infants and Children. J Pediatr. 2010;157(1):13-14.e1.
6. Grebe SK, Cooke RR, Ford HC, et al. Treatment of hypothyroidism with once weekly thyroxine. J Clin Endocrinol Metab1997;82:870-5.
Q. Is it safe to use permethrin (Nix cream, Kwellada-P lotion) to treat a breastfeeding baby for scabies?
The mother must also be treated for scabies at the same time.(8) Although the use of permethrin by breastfeeding women has not been studied, it is considered the treatment of choice for breastfeeding women.(9,10,11) Because the drug is not well absorbed through the skin, very little ends up in the breast milk and it is recommended for scabies treatment with no interruption in breastfeeding. (9,10) The manufacturer suggests that breastfeeding could be temporarily stopped while the mother is being treated (1) but this can be very inconvenient and is not necessary. Wash the cream off the nipples before nursing and reapply after the baby is finished feeding. (12)
General information about scabies
Scabies is an infestation of the skin by a burrowing mite Sarcoptes scabiei. This infestation results in extreme itchiness in the areas of the skin where the mite burrows. The itching is usually more severe at night and is caused by an allergic-type reaction to the mite, mite waste and mite eggs. Signs of the burrows or tracks are most common in the folds of the skin, between fingers, in armpits, around the waist, along the insides of wrists, inner elbow, on the soles of feet, around breasts and in the groin, although almost any area of the body can be affected. The burrow is a thin, grayish, reddish, or brownish line that is 2 to 15mm long.
Scabies is spread by close physical contact and, less often by sharing clothing or bedding with an infected person. Therefore all members of a household should be treated if one person has symptoms. Dogs, cats and humans are all affected by their own distinct species of mite. Each species of mite prefers one specific type of host and doesn't live long away from that preferred host. So, humans may have a temporary skin reaction from contact with the animal scabies mite, but people are unlikely to develop full-blown scabies from pets.
To reduce the risk of transmission or eliminate reinfestation all contacts of the scabies infested person, even if they have no symptoms, should be treated as well. This includes sexual and close personal or household contacts within the preceding month. Itching can go on for weeks after successful treatment. Continued itching is not necessarily a reason for retreatment. Antihistamines can be used to treat the itching.
Permethrin 5% (Nix, Kwellada-P)
The cream or lotion is applied two times with a week or so between each application. Permethrin is generally considered safe for children and adults of all ages, including women who are pregnant or breastfeeding.
Directions for Use: For External Use Only
1. Discontinue use of other topical medications and cosmetics during treatment.
2. Clean and dry skin.
Note: Do not take a hot bath before treatment.
3. Apply sufficient amounts of Nix dermal cream (30 g tube) or Kwellada-P lotion and thoroughly massage into the whole body, excluding the head and face (except in infants), paying special attention to creases in the skin, hands, and feet, between fingers and toes, underarms and groin as well as under fingernails. Put on clean clothes. Long-sleeved shirts, pants and mittens should be worn by young children to avoid contact with mouth.
4. Leave product on skin for 8 to 14 hours.
5. Wash off by taking a shower or a bath.
6. Change into clean clothes.
7. Scabies will be killed, but itching may persist. This is normal and does not necessarily mean that the treatment has failed.
8. One single application is effective in most cases. If necessary, a second application may be given 7 to 10 days after the first, but only if live mites can be seen or new lesions appear.
9. All clothing, bed linens, and towels used within the 2 days prior to treatment should be machine-washed in hot water and dried on dryer hot cycle for at least 20 minutes, or dry cleaned following treatment. Mattresses which have been used by an infested person should not be used for 48 hours. Toilet seats should be disinfected.
This non-insecticide medication is applied once a day for two to five days. Your doctor may recommend it if your baby has scabies. Crotamiton is considered safe in pregnancy and breastfeeding. It may not be as effective as permethrin.
Directions for Use: For External Use Only
1. Take a bath or shower before using this medication. Remove scaly or crusted skin by rubbing gently. Then dry with a towel.
2. Massage a thin layer of the cream into skin from the chin down to the toes, including skin folds and creases, between the fingers and toes, and on the soles of the feet. Avoid applying crotamiton on the face, eyes, mouth, vagina, and any skin that is inflamed, raw, or oozing. Trim fingernails short and apply the medication under the nails since the mites often live there. You may use a toothbrush to apply the medication under the fingernails. Immediately after use, wrap the toothbrush in paper and throw it away. Do not use the same toothbrush in the mouth because it may lead to poisoning.
3. Apply the medication again after 24 hours.
4. Change clothing, towels, and bed sheets the next morning after each application. Wash all clothing, towels, and bedding that have been used in the 3 days before treatment and after each application in hot water and dry in a hot dryer (or dry-clean) to kill all the mites and prevent them from returning. Items that cannot be washed or dry-cleaned should be removed from contact with the body for at least 72 hours.
5. Take a bath 48 hours after the last application to remove the medication from your skin.
Prepared by Jean Macpherson BSP and Karen Jensen MSc, BSP (SDIS). Reviewed by Dr. Yvonne Shevchuk PharmD, FCSHP (College of Pharmacy & Nutrition).
1. e-CPS [Internet]. Ottawa (ON): Canadian Pharmacists Association; c2012. Nix Dermal Cream [product monograph]. Available from: http://www.e-cps.ca. Also available in paper copy from the publisher.
2. Canadian Paediatric Society [website]. Scabies management. Ottawa, ON: Canadian Paediatric Society; 2009. Available from: http://www.cps.ca/en/documents/position/scabies. Accessed Nov. 2012.
3. Centers for Disease Control and Prevention [website]. Scabies. Suggested guidelines. Atlanta, GA: Centers for Disease Control and Prevention; 2008. Available from: www.cdc.gov/scabies/hcp/index.html. Accessed Nov. 2012.
4. United Kingdom National Guideline on the Management of Scabies infestation (2007). Available at http://www.bashh.org/documents/27/27.pdf. Accessed Nov. 2012.
5. Albakri L, Goldman RD. Permethrin for scabies in children. Can Fam Physician. 2010 Oct;56(10):1005-6.
6. Micromedex. Crotamiton monograph. Available at: http://www.thomsonhc.com/micromedex2/librarian/ND_T/evidencexpert. Accessed October, 2012.
7. Pielop J. Vesiculobullous and pustular lesions in the newborn. UpToDate, Waltham, MA, 2012.
8. Goldstein, BG, Goldstein, AO. Scabies. In: UpToDate, Ofori, AO (Ed), UpToDate, Waltham, MA, 2012.
9. Briggs G, Freeman R, Jason S. Permethrin monograph In: Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk, e-book 9th Edition. Lippincott Williams & Wilkins, 2011
10. Schaefer C, Peters P, MillerRK. Drugs During Pregnancy and Lactation, Second Edition. New York: Academic Press; 2007.
11. National Library of Medicine. Permethrin monograph. In: LactMed electronic database. Available at http://toxnet.nlm.nih.gov/cgi-bin/sis/search/f?./temp/~cZGEDf:1. Accessed November, 2012.
12. Scabies monograph. In: Patient.co.uk. Available at http://www.patient.co.uk/health/scabies. Accessed November 2012.
13. Mayoclinic. Scabies. Available at: http://www.mayoclinic.com/health/scabies/DS00451/DSECTION=treatments-and-drugs. Accessed October, 2012.
All of Saskatchewan’s supply of flu vaccines is currently from Novartis. The vaccines have NOT been recalled, but distribution and administration have been halted until analysis is complete.
1) Reason for the recall
Protein aggregates were identified in one batch of the vaccines which were NOT distributed. No aggregates have been seen in other batches of vaccines released.
A vaccine is made up of components of the virus we are protecting against. The components are different types of proteins. Sometimes, these proteins can come together and clump up, forming these protein aggregates which can be seen by the naked eye.
The protein aggregate seen in the Novartis vaccine are the expected viral proteins, not contaminants.
2) Safety issues
Protein aggregates have been seen in vaccines before. Even if they are administered to you, they do not pose any safety concerns.
Additionally, in standard vaccination procedure, the provider will look at the liquid in the vial both before and after shaking it. If protein aggregates are present after shaking, that vaccine is not administered—so no one should have been given a vaccine containing protein aggregates.
There is some concern administering a vaccine with protein aggregates could more likely trigger an allergic reaction. However, allergic reactions would be immediate. If you have already received your vaccine, there is no reason to worry.
Approximately 2 million doses of the Novartis vaccine have been given globally, with no reported adverse effects.
3) Effectiveness concerns
Available information suggests protein aggregates DO NOT reduce the effectiveness of the vaccine. Re-vaccination is not necessary. Novartis and Health Canada have thoroughly tested the vaccines, and they are as potent and effective as they should be.
4) Summary and More information
Flu vaccinations have been suspended as a precautionary measure—the vaccines have not been recalled. There are no safety issues identified or expected, and also no effectiveness issues requiring re-vaccination. For more technical information, visit this similar article prepared for health-care professionals: _________________
1. Novartis, 10 key facts at a glance - Novartis Influenza Vaccines. http://www.novartis.com/downloads/newsroom/product-related-info-center/10-Key-Facts-at-a-Glance-en.pdf
2. Novartis, Q&As with Jeffry Stoddard, Head Global Medical Affairs. http://www.novartis.com/downloads/newsroom/product-related-info-center/QAs-with-Jeffrey-Stoddard-Head-Global-Medical-Affairs-Novartis_en.pdf
3. Novartis, Information for Doctors and Patients. http://www.novartis.com/newsroom/product-related-info-center/influenza-vaccines-information-center/information-for-doctors.shtml
4. Interview with Dr. Paul Hasselback, Vancouver Island Health Authority:
5. Health Canada notification, http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2012/2012_162-eng.php
6. Interview with Dr. Allison McGeer; Infectious Disease consultant Mount Sinai Hospital, Toronto:
Isopropyl myristate (trade name Resultz) works by dissolving the outer waxy coating of the louse which causes unchecked water loss and death by dehydration. It also enters and blocks the breathing passages of the louse. Direct contact with isopropyl myristate causes rapid total paralysis of lice within minutes. It is important that all of the lice on the head of the affected person are in contact with isopropyl myristate rinse to ensure effectiveness. (1, 3) The solution is left on for 10 minutes and rinsed out with warm water. The hair can then be combed with the lice comb provided. This whole procedure should be repeated in 7 days. (3)
Dimeticone (trade name NYDA) is the most recent product approved to treat head lice. It works by suffocating lice and their nits. After application, the solution flows into the breathing system of the lice, their nymphs, and even lice embryos in their eggs, and then thickens, thereby suffocating them. (1)
The somewhat oily liquid is sprayed on to dry hair, especially the hair near the scalp and behind the ears (as this is where most lice and nits are found), massaged in until hair is completely wet and then left for 30 minutes before combing hair with the comb provided. Dosage varies depending upon thickness and length of hair. It is then left on the hair and scalp for 8 hours and washed out. The whole process should be repeated in 8 to 10 days. (4)
Both of these new treatments are well tolerated and have cure rates of up to 80% to 97% and therefore are good alternatives to the chemical treatments which have been available for much longer. (2) Because of the way these products work, it is hoped that lice will be less likely to become resistant to them.
Household products (e.g., mayonnaise, petroleum jelly, olive oil, margarine, thick hair gel) and natural products (e.g., tea tree oil, aromatherapy) should not be used because there is little evidence to prove that they are effective or safe.(5)
Prepared by Jean Macpherson, BSP, SDIS consultant; reviewed by Karen Jensen, MSc, BSP, SDIS consultant
1. PL Detail-Document, Non-insecticide Lice Treatments. Pharmacist’s Letter/Prescriber’s Letter. April 2012.
2. Dumont Z, Rutherford L. Head lice: Picking out truth from myth Pharmacy Practice 2012;28:18.
3. e-CPS [Internet]. Ottawa (ON): Canadian Pharmacists Association; c2012. Resultz [product monograph]. Available from: http://www.e-cps.ca. Accessed October 2012.
4. eCPS [Internet]. Ottawa (ON): Canadian Pharmacists Association; c2012. Nyda [product monograph]. Available from: http://www.e-cps.ca. Accessed October, 2012.
5. Management of head lice. Pharmacist's Letter/Prescriber's Letter 2008;24(11):241118.
People are first encouraged to try to keep a regular bathroom routine, to increase the amount of exercise they get as well as increase the amount of fiber in the diet (25 grams a day for women and up to 38 grams a day for men). With the increase in fiber they should also increase the amount of liquids they drink to at least 1500ml (6 cups ) a day. (2, 3) If none of these suggestions work, then laxatives are recommended.
There are three main types of nonprescription medications used to treat constipation: bulk- forming, emollient, osmotic and stimulant. In general, they should be tried in the following order:
1. Bulk- forming laxatives: These are the safest laxatives and can be used long-term. They contain bran, psyllium or guar gum (e.g. Metamucil®, Benefibre®). They may take from 1 to 3 days to work and may cause diarrhea, bloating and gas. These should be taken starting with one dose a day and increased gradually to reduce side effects. It is important to drink at least 1 cup (250ml) of water with each dose and to wait at least 2 hours before or after taking other medications as they may interfere with absorption of other drugs.
Emollients: These are also known as stool softeners. They do not have any laxative action, but may help to prevent hard stools from forming. The ingredients in these products are docusate calcium (e.g. Surfak®) or docusate sodium (e.g. Colace®). These products may take 1 to 3 days to start working.
2. Osmotic laxatives: When bulk-forming products do not work adequately the next step is to try an osmotic laxative such as lactulose (e.g.Laxilose). This causes fluid to be drawn in to the bowel to produce soft stools within 24 to 48 hours. Osmotic laxatives can cause cramping and bloating.
Glycerin suppositories are also osmotic laxatives and work within 15 to 30 minutes. These should be used only up to 3 times a week and may cause irritation around the rectum.
Other osmotic laxatives include PEG or polyethylene glycol-containing products (Lax-a-DAY®, Pegalax®, Restoralax®) and magnesium containing products (e.g. Milk of Magnesia®, Citro-Mag®).
3. Stimulant laxatives are the next step if the previous products do not work. These have ingredients which make the muscles of the large intestine contract to move the stool through and cause a bowel moment. (E.g. Dulcolax®, Senokot®) These laxatives usually work within 6 to 12 hours and are recommended to be taken at bedtime to cause a bowel movement in the morning. These may also cause cramping and abdominal pain. Although it was once thought that using these products for a long time would cause dependence or damage to the intestine, they are now considered safe and effective if used only up to 3 times a week. (1, 2, 3)
If none of these measures work there is a new prescription product for women with chronic constipation called Resotran® which may begin working as soon as 2 hours after taking a dose. A return to normal bowel movements should be expected within 4 to 5 days. (1)
Some diseases and conditions or secondary causes of constipation:
- Colorectal cancer and/or any tumors that press on the intestines
- Irritable bowel syndrome
- Cystic fibrosis
- Kidney failure
- Hirschsprung’s disease
- Multiple sclerosis
- Parkinson’s disease
- Spinal cord injury
- Scar tissue formation after surgery
- Narrowing of the bowel (stricture)
- Anal fissures
- Psychiatric or psychological conditions such as depression, dementia, eating disorders, anxiety
Some drugs that may be associated with constipation:
- Narcotic pain killers – for example, codeine, morphine, hydromorphone
- NSAIDS - for example, ibuprofen, naproxen, ASA
- Antacids and/or antidiarrheal agents which contain aluminum, calcium or bismuth
- Iron preparations
- Antidepressants – for example amitriptyline, paroxetine, venlafaxine
- Some antihypertensive drugs used to treat high blood pressure – for example verapamil, diltiazem, amlodipine, nifedipine, clonidine, methyldopa
- Antinauseants – for example dimenhydrinate, scopolamine, ondansetron
- Antihistamines – for example diphenhydramine, hydroxyzine
- Anti-seizure medications – for example, phenytoin, gabapentin, pregabalin
- Antiparkinson drugs – for example amantadine, levodopa, pramipexole
- Antipsychotic drugs –for example olanzapine, quetiapine
- Diuretics (water pills) – hydrochlorothiazide, furosemide
- Some types of chemotherapy – especially with vinca alkaloids
- Antidiarrheal drugs such as loperamide and resins such as cholestyramine
Prepared by Jean Macpherson, SDIS Drug Information Consultant. Reviewed by Karen Jensen and Carmen Bell, SDIS Drug Information Consultants
1) Battistella, Maria. Current and Future Therapies for the Management of Chronic Constipation. Available at http://www.canadianhealthcarenetwork.ca/pharmacists/ Accessed May 18, 2012
2) Patient self-care: helping your patients make therapeutic choices. 2nd edition. Published by Canadian Pharmacists Association, Ottawa ON; 2010
3) Satish SC Rao, Narasimha M Palagummi, Constipation in the older adult. In: UpToDate, Nicholas J Talley(Ed), UpToDate, Waltham, MA, Mar 2012. Accessed online May 2012.
4) Chaun,Hugh Therapeutic Choices, Gastrointestinal Disorders: Constipation in Adults. In: Gray Jean editor. eTherapeutics+[Internet].Ottawa (ON):Canadian Pharmacists Association;c2012[Date Revised: March 2012] Available from: http://www.e-therapeutics.ca. Also available in paper copy from the publisher.
Q. I have been hearing a lot about Raspberry Ketone being used for weight loss. Is it safe and effective?
There is no reliable evidence for the claim that raspberry ketone helps humans to lose weight.4,5 Two studies done on mice showed that raspberry ketone stopped them from gaining weight when they were fed high fat food, but no studies done on humans have been reported.6,7 Raspberries are known to contain high levels of anti-oxidants and one study in humans showed that it does help to lower levels of oxidants that build up during exercise.8 However, there is no proof that this will result in either weight loss or improved health.
Raspberry ketone is likely safe when used in amounts commonly found in food.4 The safety of larger doses of raspberry ketone has not been established. There is 1 to 4 mg of ketone in one kilogram (2.2 pounds) of raspberries.9 The typical dose of 250 mg of raspberry ketone therefore contains approximately the same amount of ketone as 60 or more kilograms of raspberries – a much larger dose than would be consumed in food. There are some reports of people experiencing heart palpitations (rapid, pounding heart beat) and a reduced effect of warfarin, a blood thinner.1
The raspberry ketone used in supplements is not produced from raspberries but instead is synthesized in manufacturing plants.10 No single ingredient raspberry ketone product has been approved by Health Canada.11 Purity and dose consistency of unapproved products cannot be guaranteed.
Anyone who is allergic to raspberries, blackberries, strawberries and roses may have an allergic reaction to raspberry ketone and should avoid products which contain it.5 Pregnant women should not use raspberry ketone in large amounts as it may affect labour and delivery.3,4 Because there is not enough evidence to show that it is safe, women who are breastfeeding should not take raspberry ketone.3,4 Raspberry ketone should also be avoided by people with certain cancers such as breast, uterine and ovarian cancer and by women with endometriosis and uterine fibroids as it may act like the hormone estrogen and worsen these conditions.3
Prepared by Jean Macpherson, SDIS drug information consultant. Reviewed by Dr. Jeff Taylor, College of Pharmacy & Nutrition and Karen Jensen, SDIS drug information consultant.
1. Raspberry Ketone for Weight Loss. Article; Canadian Pharmacist’s Letter; May, 2012; Vol: 19. Accessed May 16, 2012.
2. Ketones –urine. MedlinePlus. http://www.nlm.nih.gov/medlineplus/ency/article/003585.htm. Accessed May 16,2012.
3. Bitter Orange (citrus aurantium) Professional monograph, Natural Standard. Available at www.naturalstandard.com with subscription. Accessed May 16, 2012.
4. Raspberry (RED RASPBERRY) monograph. Natural Medicines Comprehensive Database electronic database. Available online by subscription. Accessed April 3, 2012
5. Raspberry (Rubus idaeus) Professional Monograph, Natural Standard. Available at www.naturalstandard.com with subscription. Accessed April 3, 2012.
6. Park KS. Raspberry ketone increases both lipolysis and fatty acid oxidation in 3T3-L1 adipocytes. Planta Med. 2010 Oct; 76(15):1654-8. Epub 2010 Apr 27. Accessed April 3, 2012.
7. Morimoto C, Satoh Y, Hara M, et al. Anti-obese action of raspberry ketone. Life Sci. 2005 May 27;77(2):194-204. Epub 2005 Feb 25. Accessed April 3, 2012.
8. Morillas-Ruiz J, Zafrilla P, Almar M, et al. The effects of an antioxidant-supplemented beverage on exercise-induced oxidative stress: results from a placebo-controlled double-blind study in cyclists.Eur J Appl Physiol. 2005 Dec;95(5-6):543-9. Epub 2005 Aug 31. Accessed April 3,2012.
9. Beekwilder, J.; Van der Meer, I.; Sibbesen, O.Microbial production of natural raspberry ketone. Biotechnol. J. 2007; 2 (10): 1270–1279. Accessed April 3, 2012.
10. Amercian Council on Science and Health. When is a doctor like a scarecrow? When he doesn’t use his brain. Available at http://www.acsh.org/factsfears/newsid.3547/news_detail.asp. Accessed April 20, 2012.
11. Health Canada. Licensed Natural Health Products Database. Available at http://webprod3.hc-sc.gc.ca/lnhpd-bdpsnh/search-recherche.do?lang=eng. Accessed April 20, 2012.
Probiotics: Products containing Lactobacillus or Saccharomyces may be effective in preventing TD.4 These can be bought without prescription in most Canadian pharmacies.4 The suggested dose is two billion organisms daily starting two days before leaving and continued for the length of the trip.7 Do not use probiotics without consulting your doctor if you have a weak immune system caused by conditions such as AIDS, certain cancers, or are undergoing long term corticosteroid treatment.8
• Drink boiled or bottled water, or use water purifiers
• Wash your hands regularly and thoroughly with water and soap or use an alcohol based hand sanitizer, especially before handling food.
• Eat thick skinned fruit that you can peel yourself, such as oranges and bananas.
• Eat well cooked food while it is hot.1,2
• Ice cubes in drinks
• Any unpeeled fruit
• Unpasteurized milk and dairy products
• Salads & buffets
• Re-heated foods
• Shellfish and large fish
• Food from street vendors
• Swimming in fresh water1,2
Antibiotics: Using antibiotics to prevent TD in healthy adults and children is not recommended. Taking antibiotics unnecessarily can lead to bacterial resistance and also may make people more likely to get other infections or have reactions to the drugs.3,4
Prevention treatment with antibiotics might be considered for travellers who must stay healthy such as business travellers or international athletes or for people with conditions that place them at higher risk for TD. This would include people with AIDS, immunodeficiency, chronic gastrointestinal disease, kidney disease and diabetes.1,2,3,5 These people may benefit from prescription antibiotics which are started on the first day in the area and continued for 1 to 2 weeks after returning home.
Vaccine: An oral vaccine called Dukoral®, which works against a common cause of TD, is sometimes used. It is available without a prescription in Canada and is taken as 2 doses by mouth at least 1 week apart. Protection takes effect 1 week after the last dose and lasts for 3 months.6
Self-treatment of TD:
Studies have shown that self treatment is effective in rapidly improving TD.3,5 Mild to moderate TD (up to 3 bowel movements per day with no blood in stool and no fever) will often get better within 24 hours with nonprescription antidiarrheal medicines such as loperamide (Imodium, generics) and bismuth subsalicylate (Pepto Bismol, generics).4 Imodium and Pepto Bismol should be avoided in severe TD.4 Pepto Bismol contains an ingredient related to aspirin and therefore should not be used by people with bleeding problems or who are taking blood thinners; pregnant or breastfeeding women; and children with flu like symptoms or chickenpox.9
Severe TD (blood in stool and/or fever) should be treated with antibiotics. Your doctor may prescribe an antibiotic for you to take with you. You can use the medicine if you do get TD. Usually, you will get enough of the medicine to last for three days. If you get better before that, you can stop taking the medicine. If you do not have a fever or blood in your stool, you can take loperamide along with your antibiotic.3,4
If you get TD it is important to avoid dehydration. You can buy oral rehydration salts such as Gastrolyte or Pedialyte to take with you. These are also sold without a prescription in most countries. Mix in distilled or boiled water.3
You should see a doctor if any effects continue for more than 2 weeks after returning home.4
Prepared by Jean Macpherson, Drug Information Consultant. Reviewed by Dr. Yvonne Shevchuk, College of Pharmacy & Nutrition, U of S and Karen Jensen, SDIS.
1) International Association for Assistance to Travelers. Available at http://iamat.org/getting_ready_travel_health_basics.cfm . Accessed Apr. 1, 2012.
2) Health Canada. Travel Health. Minimizing your risk. Available at http://www.hc-sc.gc.ca/hl-vs/iyh-vsv/life-vie/travel-voyage-eng.php#mi. Accessed Apr. 1, 2012
3) What You Should Know About Travelers Diarrhea. Canadian Pharmacists Letter; May 2007; Vol: 23.
4) Travellers Diarrhea – Treatment and Prevention. Anti-infective Guidelines for Community-acquired Infections 2010 Edition:p102-103.
5) Steeves A, Ford D. Essential intervention: The pharmacists expanding role in travel medicine. Pharmacy Practice July/August 2010.
6) e-CPS [Internet]. Ottawa (ON): Canadian Pharmacists Association; Dukoral [product monograph]. Available from: http://www.e-cps.ca. Also available in paper copy from the publisher. Accessed Apr. 1, 2012.
7) Hilton E, Kolakowski P, Singer C, et al. Efficacy of Lactobacillus GG as a Diarrheal Preventative in Travelers. J Travel Med 1997;4:41-3.
8) Health Canada. Licensed Natural Health Products Database. Culturelle monograph. Available at http://webprod3.hc-sc.gc.ca/lnhpd-bdpsnh/search-recherche.do?lang=eng. Accessed Apr. 15, 2012
9) C-Health. Pepto-Bismol monograph. Available at http://chealth.canoe.ca/drug_info_details.asp?brand_name_id=5164. Accessed Apr. 15, 2012.
Bedbugs are flat, oval, reddish-brown, wingless insects about 5 to 9 mm in length. They feed on human or animal blood. Females require a blood meal for egg production and nymphs require a blood meal for growth. Males can go for a year or more between feedings. They feed at night and are attracted by carbon dioxide which we exhale. Bites, if evident are usually on arms, shoulders, neck and legs. Presence of bedbugs is determined by the sighting of live or dead bugs, dark, reddish brown fecal or blood spots on bedding and a sweet musty odor given off by the bugs.(1,2,3)
Seven to eight percent of those bitten will have a reaction to the bites. This appears as red bumps often in clusters of three or four. The reaction may be immediate or delayed for 7 to 10 days. The bites can be extremely itchy. Vigorous scratching which breaks the skin can introduce bacteria normally present on the skin into a wound. A secondary infection may occur especially in diabetics or people who have a weak immune system. Bites can be treated with topical steroids such as hydrocortisone cream, antihistamines and/or moisturizing creams. If symptoms do not improve within one to two days or worsen, talk to your pharmacist or doctor.(1,2,3)
As for bedbugs spreading disease the evidence is somewhat limited. Bedbugs are suspected of transmitting infectious agents, but there are no reports of this actually happening.(4) In order to spread a disease the vector (bedbugs) must be able to acquire an infectious agent, maintain it, and then give it to an animal or human. A recent study in an underprivileged area of Vancouver, B.C. found antibiotic-resistant bacteria in some bedbugs but more research is needed to find out if bedbugs can spread these bacteria through their bites.(5)
Taking a few precautions while travelling is a good way to keep them from coming home with you. For information on how to avoid getting bedbugs and how to deal with them if you bring them home, Health Canada has a good website (www.hc-sc.gc.ca/cps-spc/pest/part/protect-proteger/bedbugs-punaises-lit/index-eng.php). Note that professional help is usually needed in order to rid of bedbug infestations.
Provincial and municipal public health officers are responsible for local health issues. They can provide you with the latest information you need if you find you have bedbugs. Local listings for public health officers are available at www.health.gov.sk.ca/public-health-offices .
Prepared by Jean Macpherson, SDIS drug information consultant. Reviewed by Karen Jensen and Carmen Bell, SDIS drug information consultants.
1) Canadian Pharmacist’s Letter May/09 Updated August 2011 Bedbugs – Identification,
2) Elston D, Kells S. Bedbugs. In UpToDate online database. Available at www.uptodate.com by subscription and log-in. Accessed Feb. 2012.
3) Health Canada. Bedbugs. Available at www.hc-sc.gc.ca/cps-spc/pest/part/protect-proteger/bedbugs-punaises-lit/index-eng.php. Accessed Feb. 2012.
4) Delaunay P, Blanc V, Del Giudice, P, et al. Bedbugs and infectious diseases. Clinical Infectious Diseases 2011;52:200 – 210.
5) Lowe CF, Romney MG. Bedbugs as vectors for drug-resistant bacteria. Emerging Infectious Diseases Journal 2011;17 Available at http://wwwnc.cdc.gov/eid/article/17/6/10-1978_article.htm.
In the past there was some theory to suggest that the use of saw palmetto might act to reduce the size of the prostate and thereby be helpful in the treatment of BPH symptoms. It is thought to act similarly as some prescription products, but with a much weaker effect. Past clinical research on saw palmetto is conflicting. This is further muddled by the fact that differences in the strength and purity of products on the market makes it challenging to evaluate3. However, the majority of studies which have reported a positive effect for saw palmetto have been small and poorly designed. Better quality research has failed to find any benefit for saw palmetto for BPH.(4-5) Many experts no longer recommend the use of saw palmetto for BPH.(6-8)
Some patients may still wish to try saw palmetto. In general, it is well-tolerated but there are a few side effects to watch for. Dizziness and stomach related complaints such as nausea, vomiting, constipation, and diarrhea occasionally occur. Choose a product with an NPN number; which indicates the product has been assessed by Health Canada and contains what it claims to contain. Be aware that there may not be any dramatic improvement in symptoms and if any effect is to take place it would take at least 1 to 2 months. If symptoms still continue afterwards then best to consult your physician for prescription therapy.(7)
Answered by Gurpreet Nijjar, BSc, BSP.
Reviewed by Jeff Taylor, PhD, BSP and Karen Jensen MSc, BSP
Posted December, 2011.
1. UpToDate: Medical Treatment of Benign Prostatic Hyperplasia
2. Dynamed: Benign Prostatic Hyperplasia
3. UpToDate: Clinical Use of Saw Palmetto
4. JAMA. 2011 Sep 28;306(12):1344-51. Effect of increasing doses of saw palmetto extract on lower urinary tract symptoms: a randomized trial.
5. Cochrane Review. April 2010. James Tacklind, Roderick MacDonald, Indy Rutks, Timothy J Wilt. Serenoa repens for benign prostatic hyperplasia.
6. NMCD: Natural Medicines in the Treatment of Benign Prostatic Hyperplasia
7. Canadian Pharmacists Letter. Article; Canadian Pharmacists Letter; November 2011; Vol: 27.
8. Journal Watch. Treating Lower Urinary Tract Symptoms with Saw Palmetto. Available from: http://general-medicine.jwatch.org/cgi/content/full/2011/1006/1
Q. I have already had shingles. Does this mean I am immune to future episodes of shingles, or should I still get the vaccine to prevent a recurrence?
The vaccine, called Zostavax®, protects against the herpes zoster virus, which causes chicken pox at first infection. The body never rids itself of the virus and it can show up again decades later as shingles. Up to 10 in every thousand seniors develop shingles every year. Without the vaccination, 10 percent to 14 percent of them will suffer from neuralgia (severe sharp pain along the course of a nerve). The lifetime incidence of herpes zoster is estimated to be about 20% in the general population and maybe as high as 50% among those surviving to 85 years or higher.
Individuals with prior history of herpes zoster were excluded from the Shingles Prevention Study and therefore the National Advisory Committee on Immunization makes no recommendation for Zostavax® immunization of individuals with a past episode of zoster. Nevertheless they don’t have any safety concerns for people who have already been immunized with the shingles vaccine. Persons with recent episodes (within 3 to 5 years) of herpes zoster have a boost in immunity that is as strong or better than that obtained from the zoster vaccine so they may not benefit from the vaccine, although recurrent zoster has been confirmed in some healthy patients soon after a previous episode. Individuals with a more remote history of herpes zoster may benefit because herpes zoster can recur, but there are no studies to show that getting the vaccine after having shingles actually reduces the risk of getting it again.
Zostavax® was initially approved for ages 60 and up...now the Public Health Agency of Canada recommends it for ages 50 and up.
ZOSTAVAX® reduces the lifetime risk of developing zoster compared with no treatment by 10% in the general population.
Answered by Lisa Hupka, Bsp
1. Twersky Jack I, Schmader Kenneth, "Chapter 129. Herpes Zoster" (Chapter). Halter JB, Ouslander JG, Tinetti ME, Studenski S, High, KP, Asthana S: Hazzard’s Geriatric Medicine and Gerontology, 6e: http://www.accessmedicine.com/content.aspx?aID=5138293.
2. http://www.phac-aspc.gc.ca/ccdrw-rmtch/2011/ccdrw-rmtcs0211-eng.php. Canadian Communicable Disease Report. Infectious Diseases News Brief - January 14, 2011
3. Canadian Pharmacist’s Letter; May 2011; Vol: 27
4.10.3949/ccjm.75a.08046 Cleveland Clinic Journal of Medicine. January 2009 vol. 76 1 45-48 Who should receive the shingles vaccine? Aparajita Singh, MD, MPH
5. http://www.merck.ca/assets/en/pdf/products/ZOSTAVAX-PM_E.pdf ( accessed October,2011)
Usually no other treatment is necessary, but if swelling, itching or pain occur and are bothersome treatment with a topical analgesic ( benzocaine, lidocaine etc. ), steroid cream ( hydrocortisone ), counter irritant ( e.g. After Bite®) or skin protectant ( zinc oxide, calamine lotion ) is appropriate. Oral pain medications can be used for pain and oral antihistamines can also relieve itching. In patients who are highly sensitive to insect bites, nonsedating antihistamines taken on a regular basis can reduce the subsequent skin reactions such as itching and swelling from insect bites.
Most wasp stings do not become infected, although this can occur. The stings of yellowjackets are more likely to become infected than those of other species . Yellowjackets tend to scavenge around rotting food and presumably carry bacteria on their exterior.
Infection is suspected when redness, swelling, and pain become dramatically worse three to five days after the sting, when typically symptoms should be disappearing. The presence of fever also suggests infection. Mild symptoms can be treated with a topical antibiotic (e.g. Polysporin® ). If symptoms do not improve within 48 hours, you should see a doctor. An oral antibiotic may be needed.
Some people who are allergic to the wasp venom will have a severe reaction to a wasp bite and symptoms may include chest tightness, difficulty breathing, swelling of the tongue, throat, nose, and lips, dizziness, and/or loss of consciousness. Complications may include shock and heart failure. In these cases emergency medical help should be contacted immediately. People who know that they react severely to an insect bite should carry epinephrine ( EpiPen®, or Twinject®) for emergency self-administration. They can also consider venom immunotherapy to desensitize them.
1. Canadian Pharmacist’s Letter 2008; 24(8):240815.Management of Insect Bites. ( accessed August 31st, 2011 )
2. Medscape Medical News AAAAI, ACAAI Update Stinging Insect Guidelines, Laurie Barclay, MD June 14, 2011 ( accessed August 31,2011 )
3. Theodore Freeman, MD. Bee, yellowjacket, wasp, and other Hymenoptera stings: Reaction types and acute management. UpToDate, Last updated January 2011 ( accessed Sept. 6th,2011 )
Q. Can I use products with DEET to repel mosquitoes, ticks and other insects while I am pregnant?
Exposure to DEET can be limited by wearing long sleeved shirts and leg coverings to avoid biting insects and applying this agent only to exposed skin or clothing. Also use mosquito netting, screens on doors and windows and limit the time spent outdoors between dusk and dawn.
However, the repellent DEET (N,N-diethyl-3-methyl-benzamide, also known as N,N-diethyl-m-toluamide) is acknowledged as the most effective repellent. DEET has been used as a repellent for more than 50 years and is estimated to be applied several hundred million times yearly by North Americans alone. Scientific reviews have concluded that, when used as directed, DEET has an excellent safety record.
DEET can be sprayed on clothes, but can damage certain synthetic clothing such as spandex and rayon. Cotton and wool materials are not affected.
The higher the DEET concentration in the repellent formulation, the longer the duration of protection; this relation reaches a plateau at about 30% to 35%. Products with 10% DEET work for about 3 hours and products with 30% DEET work for 6 hours.
When there is a substantial risk of getting a disease from a mosquito or a large mosquito population, it is appropriate for pregnant women to use the concentration recommended for non-pregnant adults. Otherwise, when the purpose is primarily to avoid nuisance bites a lower concentration of DEET is advisable.
Answered by: Lisa Hupka, BSP
1. www.thomsonhc.com/micromedex2/ Reprotox ( Accessed on July 6, 2011 )
2. Insect Repellents. Canadian Pharmacist’s Letter; July 2010; Vol: 26
3. Christof Schaefer, Paul Peters, Richard K. Miller. Drugs During Pregnancy and Lactation 2nd ed. Elsevier BV; 2007, PG 458-9.
4. Prevention of arthropod and insect bites: Repellents and other measures. UpToDate. ( Accessed on July 6, 2011 )
5. www.cdc.gov/travel/ Travelers’ Health ( Accessed July 6, 2011)
6. The Merck Manual for Health Care Professionals. Malaria. ( Accessed July 6, 2011 )
7. Karen Jensen. Buzz Off - Helping patients select and properly use insect repellents. Pharmacy Practice. June 1, 2011
Concern has arisen over an ingredient in some sunscreens called retinyl palmitate. It is an inactive ingredient, a type of topical vitamin A. In skin it converts readily to retinoids which are associated with a risk of birth defects in people taking oral acne medications containing them. However, the animal studies which showed birth defects used much higher doses than can be absorbed through the skin. Studies on rats have not shown sunscreen to cause malformations.
The American College of Obstetricians and Gynecologists recommends that pregnant women protect their skin from the sun by wearing sunscreen with SPF ( sun protection factor ) of 15 or more.
Sun exposure will darken dark brown areas around the eyes, nose and cheeks called cholasma or “mask of pregnancy” which some women develop ( about 70% ) during pregnancy. Sun screen and wearing a wide brim hat can prevent these areas from getting darker.
Here are other steps that Health Canada recommends you take to protect against UV exposure:
• If possible, avoid being in the sun between 11:00 a.m. and 4:00 p.m.
• Look for shade, stay under a tree, or use an umbrella.
• During outdoor activities, wear sunglasses to protect your eyes. When the UV index is three or higher, you should also wear protective clothing and a large-brimmed hat.
Topical absorption of sunscreen is minimal. Sunscreen is safe and recommended for use during pregnancy.
Answered by: Lisa Hupka, BSP
1. Nohynek GJ, Meuling WJ, Vaes WH, Lawrence RS, Shapiro S, Schulte S, Steiling W, Bausch J, Gerber E, Sasa H, Nau H. Repeated topical treatment, in contrast to single oral doses, with Vitamin A-containing preparations does not affect plasma concentrations of retinol, retinyl esters or retinoic acids in female subjects of child-bearing age. Toxicol Lett. 2006 May 5;163(1):65-76. Epub 2005 Oct 21. PMID: 16243460
2. CBC News. Sunscreen benefits beat risks in pregnancy: MDs. Posted: May25,2011. www.cbc.ca/news/health/story/2011/05/25/sunscreen-pregnancy.html
3. http://www.hc-sc.gc.ca/hl-vs/iyh-vsv/life-vie/sun_soleil-eng.php, accessed June 1, 2011
4. Using Sunscreens, 07/08/2010, Texas Tech University Health Sciences Center, www.infantrisk.com
UVA rays do not cause sunburns, but they do contribute to skin cancer and sun-related skin aging. Sunscreens, which have been around for more than 70 years, used to just protect against UVB rays, which cause sunburns and skin cancer. It is important to choose a product which protects against both UVA and UVB rays.
UVA filtering and blocking ingredients are oxybenzone, avobenzone ( Parsol 1789 ), titanium dioxide, zinc oxide and ecamsule (Mexoryl SX/XL). Helioplex, a patented combination of avobenzone and oxybenzone with stabilizers, provides protection against the full spectrum of UVA and UVB radiation. Ecamsule itself is photostable, but only covers short UVA II wavelengths. The combination with avobenzone ( absorbs the long UVA wavelengths ) and octocrylene also provides coverage against the full spectrum of UVA and UVB radiation.
The almost universal use of the sun protection factor (SPF) has lured many consumers into thinking that a higher SPF means a better sunscreen. Because SPF is mostly an indicator of UVB protection, it is difficult for consumers and physicians to compare the UVA protection afforded by sunscreens.
In many countries, changes in labeling guidelines will make it easier for consumers and physicians to determine the level of UVA protection provided by sunscreens. The FDA has proposed a UVA star rating, with one star representing low UVA protection and four stars representing the highest available UVA protection in an over-the-counter sunscreen product. Although this rule has not yet been finalized, a small number of sunscreens may have a star rating on the label.
The Canadian Cancer Society recommends the following:
• People reduce their exposure to the sun, particularly between 11 a.m. and 4 p.m. when the sun’s rays are the strongest
• Use a broad spectrum sunscreen ( protection from UVA and UVB rays )
• Choose a product that is water resistant with an SPF of at least 30
• Apply sunscreen liberally and frequently ( every 2 hours ), especially after swimming or sweating
An average size adult needs an ounce (2 tablespoonfuls ) of sunscreen for optimal coverage.
Answered by Lisa Hupka,BSP
1. Burnett ME, Wang SQ. Current sunscreen controversies: a critical review.Photodermatol Photoimmunol Photomed. 2011 Apr;27(2):58-67. doi: 10.1111/j.1600-0781.2011.00557.x. PMID: 21392107
2. Update on Sunscreens, R. Bissonnette, MD, FRCPC Posted: 11/10/2008; Skin Therapy Letter. 2008;13(6):5-7, www.medscape.com/viewartcile/5829902
3. Canadian Pharmacist’s Letter 2009; 25(6):250606, Sunscreens: Achieving Optimal Protection
4. Canadian Cancer Society. www.cancer.ca ( accessed May24, 2011 )
Q. I had heard that calcium supplements can increase the risk of having a heart attack. Is this true? I thought calcium was good for a person!
A recent analysis of calcium supplement use and cardiovascular (heart and blood vessel) risk revealed that calcium supplements with or without vitamin D, modestly increase the risk of cardiovascular events, especially heart attacks.
There does not seem to be a dose response relationship between calcium supplements and the risk of cardiovascular events. Thus even doses of less than 500mg/day might be associated with an increased risk of cardiovascular events similar to doses greater than 1000mg/day. The abrupt change in the concentration of calcium in the blood after supplement consumption seems to cause the adverse effect, rather than it being related to the total calcium dose taken.
Further studies are needed to reassess the role of calcium supplements in osteoporosis management. In the meantime a person should try to get their calcium needs met through their diet. If you are at high risk of fractures, consult your doctor before stopping or reducing your daily calcium supplement.
Dairy products such as milk, cheese and yogurt are excellent sources of calcium. Vegetables (broccoli, cabbage, bok choy, figs ) also provide calcium as do fish products containing bones (sardines and canned salmon), lentils, beans, tofu and almonds.
Calcium loss through the urine is increased by the consumption of excess salt and caffeine. Therefore try to keep salt intake to a minimum and increase calcium in your diet if you consume more than 4 cups of coffee per day.
Adults age 19 to 50 need 1000mg of calcium per day and teenagers and older adults need slightly more.
One cup of milk or low fat yogurt provide approximately 300mg of calcium each. Go to http://ods.od.nih.gov/factsheets/calcium/ to find out how much calcium is provided by the food you eat to help you plan to get the required calcium from your diet. If you have any difficulty in determining how to obtain your daily calcium requirement, please feel free to contact us.
Answered by Lisa Hupka,BSP
2. Calcium, Vitamin D, and Risk of Cardiovascular Events: Discussion www.medscape.com/viewaraticel/741974_2
3. Canadian Pharmacist’s Letter 2011; 27(1): 27012
4. Abrahamsen B, Sahota O. BMJ 2011; 342: D2080 – Do Calcium plus Vitamin D Increase Cardiovascular Risk.
Q. My friend is taking pain medication for a chronic condition. Will he become addicted to the medication?
Patients with pain rarely develop abuse or addiction problems. The patient who is not vulnerable to addiction will not experience brain reward when using controlled drugs as prescribed and therefore will not misuse prescribed medications.
The onset of abuse or addiction usually happens before the use of prescribed controlled drug use. Individuals who are at risk of addictive disease usually start their addiction through the use of alcohol, tobacco or marijuana in their late teens or early adulthood. Abuse of prescription drugs tends to complicate pre-existing addiction rather than to cause addiction.
Addiction is entirely different than physical dependence and tolerance. Although these changes presumably occur commonly as addiction develops, neither are necessary for addiction to occur, and equally important, neither means that abuse or addiction is occurring.
Inappropriate fear of addiction on the part of patients (or their caretakers) is a common reason for under-use of prescribed medications. A person should not be denied adequate pain relief because of this fear. For treatment of most types of severe pain strong opioid pain medications are the drugs of choice. Some of the problems of dependence and tolerance can be managed by using long acting formulations and gradually reducing the medication, if it is no longer needed.
Answered by: Lisa Hupka,BSP
1. O’Brien Charles P, "Chapter 23. Drug Addiction and Drug Abuse" (Chapter). Brunton LL, Lazo JS, Parker KL: Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 11e: http://www.accessmedicine.com/content.aspx?aID=941547
2. UpToDate- Prescription Drug Abuse. Desktop19.1
3. The Medical Letter. Drugs for Pain. April1, 2010(Issue 92) p.25
Q. How can I tell if a medication or vitamin product sold on the shelf has gluten in it? I have celiac disease (gluten intolerance ).
Note that avoiding gluten does not have any known health benefits for people who do not have celiac disease. (3)
In the area of pharmaceuticals, potential sources of gluten contamination come primarily from the addition of the excipient (filler), ingredients added to the active drug in order to make a particular dosage form. (1) Having an understanding of the fillers origin or how they are produced can help a person make an educated assessment of the likelihood of gluten contamination. One of the first key words to look for in the inactive ingredients list is starch. Starch can be derived from several sources including corn, potato, tapioca and wheat. If starch is listed by itself a call to the manufacturer is the only way to confirm the source of the starch. A product with cornstarch can be assumed to be gluten free.(1)
Also watch out for the four dex-ingredients derived from starch (dextrans, dextrose, dextrates, dextrins ). Dextrans come from corn and potato starch, dextrose comes from corn. Dextrates and dextrins can come from any starch source so a call to the manufacturer is necessary to find out if the product contains gluten.(1)
A problem faced by the pharmaceutical manufacturers is the uncertainty of the gluten free status of the raw materials obtained from outside sources. A person looking for gluten free products must also be aware that pharmaceutical companies frequently change the inactive ingredients of their products without warning. If a product says “new and improved” or “new formulation” it is a sign to recheck the gluten status of the product.(1)
Currently in Canada a natural health product can be labelled “gluten free” if it contains a maximum limit of 20 ppm gluten. This would be gluten from wheat, including spelt or kamut, but not barley or rye as they are not used in the preparation of medications.(1) This maximum level is based on good manufacturing conditions aimed at achieving the lowest possible levels of gluten resulting from cross-contamination.(4)
Tolerance to gluten varies among individuals with celiac disease and there are limited clinical scientific data on the amount of gluten required to initiate or maintain an immune reaction in celiac disease patients. Therefore, there is no clear agreement on a safe gluten threshold level.(4)
There are proposed changes to the Food and Drug Act to prevent products which contain trace amounts of gluten, confirmed by testing to be < 20 ppm gluten, from making the claim gluten-free.(4)
The product package insert is a good starting place to look for gluten in medications. Enrolling the help of a pharmacist will also be beneficial or call the Saskatchewan Drug Information Service at 1-800-665-3784, in Saskatoon 966-6378, to help you with the search.
Answered by: Lisa Hupka, Bsp
1.Steven Plogsted. Medications and Celiac Disease- Tips From a Pharmacist. The Celiac Diet, Series #5. Practical Gastroenterology. January 2007.
2."Gluten-Free" Foods May Be Contaminated: Study. J Am Diet Assoc 2010;110:937-940. www.medscape.com/viewarticle/725315 (accessed March 8, 2011)
3.Gluten Free Diet. May 2010. AAFP conditions A to Z (2010) Stat!Ref ( accessed March 8, 2011)
4.Notice-Labelling of Natural Health Products Containing Gluten. January 2010. www.hc-sc.gc.ca. ( accessed March 8, 2010)
Q. Am I still protected if I was late getting the 3rd injection of Hepatitis A and B vaccine? I had the first 2 Twinrix injections 10 years ago and then I had the 3rd shot 6 years later. Was this too far apart for protection from Hepatitis A and B? Do I need to do the series again or get a booster vaccination before travelling to areas where Hepatitis A and B are common?
Increasing the interval between the first 2 doses has little effect on the development of immunity or final antibody concentration for the Hepatitis B component of the vaccine. The third dose ensures the maximum level of protection but acts primarily as a booster and appears to provide optimal long-term protection.(1)(3)
The effectiveness of 1 dose of Hepatitis A vaccine ( equivalent to 2 doses of Twinrix) is 94% to 100%. Antibody production is considered to be complete after the first dose, however, the vaccine series should be finished to assure long-term protection.(5)
All available data on single and combined Hepatitis A and Hepatitis B vaccines indicates that there is no support for a Hepatitis A or Hepatitis B booster when a complete primary vaccination course is offered to individuals with a competent immune system.(4) Immune system memory has been demonstrated in a number of studies for both Hepatitis A and Hepatits B, with the implication that protection may persist even when antibodies are no longer measurable.(4)(2)
In summary, the last dose in the series is mainly to ensure long term protection and can be done any time after the first 2 doses as long as there is a minimal spacing of 24 weeks from the first dose in the regular schedule and 1 year from the first dose in the rapid schedule.
Answered by: Lisa Hupka, Bsp, February 2, 2011
1.A Comprehensive Immunization Strategy to Eliminate Transmission of Hepatitis B Virus Infection in the United States. MMWR Dec23,2005/Vol.54 http://www.cdc.gov/mmwr/PDF/rr/rr5416.pdf
2. Canadian Immunization Guide 7th ed. 2006 www.phac-aspc.gc.ca (accessed Feb2,2011)
3.High immunogenicity of delayed third dose of hepatitis B vaccine in travellers. Vaccine. 2007 Apr 30;25(17):3482-4. Epub 2007 Jan 11. PMID: 17306910
4. A review of the long-term protection after hepatitis A and B vaccination. Travel Med Infect Dis. 2007 Mar;5(2):79-84. Epub 2006 Jun 19. PMID: 17298912
5. Immunization Action Coalition Ask the Experts http://www.immunize.org/askexperts/experts_hepa.asp ( accessed Feb2,2011 )
The 2010 to 2011 flu vaccine will protect against an influenza A H3N2 virus, an influenza B virus and the 2009 H1N1 virus that caused so much illness last season.(6)
All ages benefit from getting the influenza vaccine. Exceptions are anyone under six months of age or with severe egg allergies. These groups should not be vaccinated.(2)(4) Also anyone who had a serious allergic reaction to a previous dose of influenza vaccine or who developed Guillain-Barre Syndrome ( a neurological disorder ) within 8 weeks of a previous influenza vaccine should not receive the vaccine.(2)(4)
Health Canada says between 4,000 and 8,000 Canadians mostly seniors; will die from pneumonia related to flu and many others may die from other serious complications of flu.(4) The following groups of people are at higher risk of complications from the influenza virus, such as pneumonia:
People over 65 or older.
Children 6 months to 4 years
People severely obese
People of any age who are residents of nursing homes and other chronic care facilities
Anyone with chronic health conditions
Close contacts of persons who are in the high risk of complications groups above should also get vaccinated.(1)(2) Children younger than 6 months are at high risk of serious flu illness, but are too young to be vaccinated. People who care for them should be vaccinated instead. (6)
Antiviral treatment is available and can reduce the duration and severity of illness for a person infected with the influenza virus. Antiviral treatment of influenza is most effective when administered early in the course of illness, and ideally should be administered within 48 hours of onset of symptoms. Antiviral treatment should be started in people with confirmed or suspected influenza who are at a greater risk for complications.(3)
The signs and symptoms of influenza are fever, headache, fatigue, muscle pain and weakness. These symptoms may be accompanied by cough and sore throat. Some people also experience vomiting and diarrhea.(2)(5)(6)
Seek immediate medical attention for the following symptoms in adults:
Difficulty breathing or shortness of breath
Pain or pressure in the chest or abdomen
Severe or continuous vomiting
Flu-like symptoms that improve but then return with fever and worse cough (6)
Answered by Lisa Hupka,Bsp. Jan24/2011
1.Saskatoon Health Region. Seasonal Influenza Vaccine. www.saskatoonhealthregion.ca (accessed Jan. 24. 2011
2. Public Health Agency of Canada. About Season Influenza www.phac-aspc.gc.ca (accessed Jan24. 2011)
3. Medscape Medical News. ACIP Up Dates Guidelines for use of Antiviral Agents for Influenza. Jan 21, 2011 www.medscape.com/viewarticle/736109
4. CBC News. Fighting The Flu. Jan. 14,2011 www.cbc.ca/health/stsory/2009/01/12/f-flu.html
5. UpToDate- Clinical Manifestations and Diagnosis of Seasonal Influenza in Adults. Last literature review version 18.3 Sept.2010
6. Centers for Disease Control and Prevention. Seasonal Influenza. www.cdc/flu/protect/preventing.htm (accessed Jan. 24.2011)
7. Regina Qu’Appelle Health Region. Telephone Directory for Facilities and Services. www.rqhealth.ca/inside/contact_us/phone.shtml (accessed Jan.24/2011)
It works by reducing the production of chemicals in the body that enable the body to feel pain as well as cooling the body. While acetaminophen may be helpful to reduce pain and/or fever it will not cure any medical condition.
The normal dose of acetaminophen for pain or fever in adults is: orally 325 to 650 mg every 4 to 6 hours or 1000 mg 3 to 4 times/day; do not exceed 4 g/day.
The normal dose of acetaminophen in children for pain or fever is: Children <12 years: orally 10 to 15 mg/kg/dose every 4 to 6 hours as needed; do not exceed 5 doses (2.6 g) in 24 hours or 75mg/kg/day.
Many people do not know that Tylenol is the brand name for acetaminophen and that overdose of this product can cause serious liver damage, especially when combined with other medications that can also cause damage to the liver.
Early symptoms of overdose can include nausea, vomiting, weakness, and profuse sweating. These usually occur after an ingestion of acetaminophen large enough to cause hepatic ( liver ) toxicity. However, since some patients show few or none of these early signs, in cases of suspected acetaminophen over dose, therapy should begin as soon as possible. A delay period of 24 to 36 hours exists between ingestion and the onset of symptoms of hepatic injury. Some other symptoms of toxicity are abdominal pain, confusion, a general feeling of discomfort, yellowing of skin and eyes, coma and in severe cases death.
If you suspect someone has taken too much acetaminophen phone the poison control center at 1-866-454-1212.
A situation which has potential for overdose is the practice of alternating doses of acetaminophen and ibuprofen for treatment-resistant fevers. There is no evidence that this works better than either product used alone at optimal doses. This is not recommended because of the possibility of confusion as to what medication was given, which could lead to overdose.
Another problem with acetaminophen is that it is added to many cough and cold products as well as other combination pain killers and muscle relaxants. These products may not be made by the company that makes Tylenol and therefore these products will have different names. As a result when people take these medications they may not realize the amount of acetaminophen actually being consumed, unless they have carefully read the ingredients.
To avoid this situation always read the ingredients of over the counter medications and prescription medications. Don’t exceed the dose recommended on the package and don’t take 2 products that both contain acetaminophen. If unsure, ask your pharmacist or phone Saskatchewan Drug Information Services at 1-800-665-3784 in Saskatchewan or 966-6378 if in Saskatoon.
2.Compendium of Pharmaceuticals and Specialties Online
3. Canadian Pharmacist’s Letter; July 2006; Vol: 22
Dietary Reference Intakes (DRIs) are recommendations for nutrient intakes based on Estimated Average Requirement (EAR), Recommended Dietary Allowance (RDA), Adequate Intake (AI) and Tolerable Upper Intake Level (UL).
Vitamin D is a nutrient that helps the body use calcium and phosphorous to build and maintain strong bones and teeth. Too little vitamin D can cause calcium and phosphorus levels in the blood to decrease, leading to calcium being pulled out of the bones to help maintain stable blood levels. This can cause rickets in children and osteomalacia (softening of the bones) or osteoporosis (fragile bones) in adults.
However, too much vitamin D can cause too much calcium to be deposited in the body, which can lead to calcification of the kidney and other soft tissues including the heart, lungs and blood vessels.
The IOM finds that the evidence supports a role for vitamin D and calcium in bone health but not in other health conditions.
The IOM expert committee reviewed a number of health outcomes that could potentially be related to calcium and vitamin D, such as cancer, cardiovascular disease, diabetes, and immunity, and found that the evidence was inconsistent and did not demonstrate a cause-and-effect relationship. Consequently, these health outcomes could not be used for the purposes of determining nutrient requirements.
The skin produces vitamin D3 in response to sun exposure. But the American Academy of Dermatology recommends avoiding sunlight and getting vitamin D from food or supplements. The Canadian Dermatology Association offers similar advice
The sun is not strong enough to make vitamin D in the skin in southern Canada from November to February...and for an even longer period at higher latitudes.
Few foods contain much vitamin D. Salmon, canned tuna, and fortified milk (100 IU per cup) are among the best sources. Very few foods naturally have vitamin D. Fortified foods provide most of the vitamin D in our diets.
•Fatty fish such as salmon, tuna, and mackerel are among the best sources.
•Beef liver, cheese, and egg yolks provide small amounts.
•Vitamin D is added to many breakfast cereals and to some brands of orange juice, yogurt, margarine, and soy beverages; check the labels.
New Reference values for daily intake of Vitamin D are:
Birth to 12 months 400 IU
Children 1–13 years 600 IU
Teens 14–18 years 600 IU
Adults 19–70 years 600 IU
Adults 71 years and older 800 IU
Pregnant and breastfeeding women 600 IU
New Reference values for daily intake of Calcium are:
Birth to 6 months 200 mg
Infants 7–12 months 260 mg
Children 1–3 years 700 mg
Children 4-8 years 1,000 mg
Children 9–13 years 1,300 mg
Teens 14–18 years 1,300 mg
Adults 19–50 years 1,000 mg
Adult men 51–70 years 1,000 mg
Adult women 51–70 years 1,200 mg
Adults 71 years and older 1,200 mg
Pregnant and breastfeeding teens 1,300 mg
Pregnant and breastfeeding adults 1,000 mg
Total vitamin D intake should remain below the level of the new UL (upper tolerable limit) to avoid possible adverse effects. The UL is the maximum daily intake unlikely to result in adverse health effects. The new UL is 4,000 IU daily for people from age 9 to age 70, whereas the old UL was 2,000 IU daily.
It is preferable that an individual get their recommended calcium from food sources.
Q. Why can’t my pharmacy supply me with the medication I need? They say it is shorted by the manufacturer.
This supply problem can arise from a variety of different causes including:
• Manufacturing issues
• Shortages in raw materials due to natural disasters and regulatory decisions related to the safety, efficacy or quality of a product
• Reduced inventories carried by pharmacies, wholesalers and manufacturers because of pressure to keep inventories low can result in not enough product on hand to buffer a shortage.
• Lower prices can contribute to a shortage. Recent controls in Ontario and other provinces are reducing profit, which then puts pressure on manufacturers to discontinue unprofitable products.
• Competition in the drug market causes manufacturers to discontinue making a drug if they don’t expect to have a reasonable share of the market due to policies like bulk buying or tendering. Some products coming off patent are not being made generic.
Current shortages are blamed on a shortage of raw materials and compliance issues that led to voluntary recalls of certain drugs and slower production times at manufacturing facilities. This in turn created a backlog of unfilled orders, which is expected to gradually disappear as production steps up. Even then, however, the current market and regulatory trends governing pharmaceutical sales are likely to result in ongoing generic shortages.
Health Canada has no authority to require a manufacturer to bring a product to the Canadian market or to maintain adequate supplies on the market to meet the needs of patients.
Possible actions for Health Canada are:
• Prohibit bulk exports of pharmaceuticals as a proactive move.
• Issue compulsory licences if a patent holder is unable to provide a needed product.
• Develop a list of medically essential drugs (possibly following the list provided by the World Health Organization -- WHO), and monitor and track these.
• Allow parallel importation schemes similar to those used in Europe.
• Provide notification of where products are being manufactured.
The Minister of Health intends to table legislation in Parliament, before it adjourns in December, to establish statutory authority to prohibit the export of prescription and other essential drugs from Canada as necessary to protect human health in the event of an actual or potential shortage.
If the medication you are taking becomes unavailable your pharmacist will work with your doctor to find an appropriate alternative until the shortage is resolved. If a substitute drug or different dosage strength/formulation is being used, your pharmacist will educate you about the change and what to expect.
To ensure that your drug therapy is not interrupted, don’t wait until you are out of your prescription(s) before re-ordering. If there is a shortage your pharmacist may need a few days to arrange for and obtain a suitable alternative.
Q. I heard on the news today that people on bisphosphonates for osteoporosis have been having long bone fractures and some researchers think it is related to the drug. Is this true?
The bisphosphonates available in Canada are: alendronate ( Fosamax ), risedronate ( Actonel ), etidronate/calcium ( Didrocal ) alendronate/vitamin D3 ( Fosavance ) and zoledronic acid ( Aclasta ).
The major problem in osteoporosis is fractures (broken bones). Without proper treatment, patients with osteoporosis are more likely to have fractures, commonly of the hip, spine, wrist and shoulder. The occurrence of a hip fracture is one of the ways that osteoporosis can be diagnosed. These are called typical femoral fractures and occur high up on the femoral bone, very close to the hip joint. These often occur after a fall when the hip breaks from hitting the ground. The hip does not hurt before it breaks. The person may or may not be on osteoporosis medications.
Several case series and multiple individual case reports suggest that some femoral shaft (thigh bone) fractures might occur in patients who have been treated with long-term bisphosphonates. Several unique clinical features are emerging which distinguish these fractures from typical femoral fractures which occur in osteoporosis because of the disease process itself. These features are thigh pain and/or groin pain for several weeks prior to the fracture, complete absence of an injury occurring before the fracture, fractures in both legs in some patients, the fracture occurs lower down from the hip ( closer to the middle of the femur ) and most patients with this type of fracture have been on bisphosphonates for more than 5 years. X-rays, including bone scan and/or MRI, might be warranted in patients who have femoral pain to try to find these atypical fractures at an early stage (stress fracture vs complete fracture).
The supposed mechanism is unknown, and more research is needed to identify distinctive characteristics of these “atypical” fractures. There is no rationale to withhold bisphosphonate therapy from patients with osteoporosis, although continued use of bisphosphonate therapy beyond a treatment period of 3 to 5 years should be re-evaluated annually. Women and men at low risk of fracture should discuss with their doctor if they need to continue with the bisphosphonate beyond 5 years.
For women at high risk for vertebral fractures, the National Osteoporosis Foundation (NOF) recommends continuing alendronate for ten years. Eight year data with risedronate indicated good tolerability and safety.
The risk factors that have been demonstrated to be most predictive of fracture are:
1. low bone mineral density ( BMI )
2. advancing age
3. prior history of fragility fracture
4. chronic glucocorticoid use
5. low body mass index (BMI)
6. parental history of hip fracture
7. cigarette smoking
8. excess alcohol intake
Although this recommendation is based on data from women, such treatment approach is also reasonable for men taking bisphosphonates.
Treatment with bisphosphonates reduces the risk of hip and other non-vertebral fractures by 1000 per 100,000 patient years. If a person has osteoporosis they are at high risk of fracture and much more likely to suffer a typical fracture if not treated, than of ever getting one of these “atypical” femoral fractures while on medication. If you have an increase risk of fracture, the benefits of bisphosphonates far outweigh the risks.
The overall incidence of shaft fractures combined is below 30 per 100,000 person-years, so this type of fracture is much less common than proximal femur (hip) fractures. Furthermore, the unique “atypical” fracture type is a subset of all femoral shaft fractures and accounts for less than 1% of all femoral fractures, making it a rare event.
1. Clinical Orthopaedics and Related Research
DOI: 10.1007/s11999-010-1535-x Femoral Insufficiency Fractures Associated with Prolonged Bisphosphonate Therapy.
Joseph D. Isaacs, Louis Shidiak, Ian A. Harris and Zoltan L. Szomor PMID: 20809164
2. Curr Osteoporos Rep. 2010 Mar;8(1):34-9.
Atypical subtrochanteric and femoral shaft fractures and possible association with
Nieves JW, Cosman F. PMID: 20425089
3. Safety of long-term bisphosphonate therapy. Pharmacist’s Letter/Prescriber’s Letter 2009;25(12):251205.
4. Osteoporosis Canada
5. UpToDate – Osteoporotic fracture risk assessment.
6. Clin Endocrinol Metab. 2010 Apr;95(4):1555-65. Epub 2010 Feb 19.
Long-term use of bisphosphonates in osteoporosis.
Watts NB, Diab DL. PMID: 20173017
Q. My child vomited 30 minutes after I gave him his medication. Should I give him another dose now or wait until the next scheduled dose?
The stomach has a relatively large surface area, but its thick mucous layer and short time in contact with the medication limit absorption. Most absorption occurs in the small intestine. Stomach emptying and therefore drug absorption is affected by many variables. Factors that affect how fast the stomach empties and absorption include the dosage form (liquid versus immediate release versus sustained release tablets), the physical and chemical properties of the drug, and the physiologic characteristics of the person taking the drug. Food, especially fatty food, slows stomach emptying (and rate of drug absorption), explaining why taking some drugs taken on an empty stomach speeds absorption.
You can redose if vomiting occurs within 15 minutes...or if you see the intact drug in the vomit . After an hour, there’s usually no need to redose because the drug is probably already past the stomach. But if vomiting occurs within the 15- to 60-minute window, you must consider the risk versus benefit of repeating the dose.
If the risk of missing a dose outweighs the risk of getting too much of the drug, as with drugs such as HIV meds and birth control pills, then it is important to give another dose if a patient vomits within an hour.
Antibiotics for acute infections, especially with a single dose treatment or short course of therapy, should also be given again if the patient vomits within an hour of administration.
For many drugs it is best to err on the conservative side and not give another dose. This is very important for drugs whose recommended dose is close to the toxic dose (narrow therapeutic window ) and getting a bit more of the drug could result in too much with serious consequences.
Examples of drugs not to redose are digoxin, warfarin, phenobarb, long acting opioids, methotrexate, cyclosporine, theophylline, lidocaine, aminoglycosides and other anticonvulsants.
Always check with a health care professional to be sure of the medication in question.
1. Redosing oral medications after vomiting. Pharmacist’s Letter/Prescriber’s Letter 200;25(9):250909
3. Buxton Iain L, “Chapter 1. Pharmacokinetics and Pharmacodynamics: The Dynamics of Drug Absorption, Distribution, Action, and Eliminatio” (Chapter). Brunton LL, Lazo JS, Parker KL: Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 11e: http://www.accessmedicine.com/content.aspx?aID=935800
The typical incubation period for infection ranges from 2 to 14 days. Once a patient recovers, immunity to West Nile virus is thought to be life-long; if reinfection occurs, it is very rare.
The most common symptoms are fatigue, fever, headache, skin rash, muscle weakness, diarrhea, vomiting, pain in your eyes, not feeling hungry, swollen glands (rarely) and/or difficulty concentrating. The rash typically involves the chest, back and arms, and generally lasts for less than one week. Most people who have the mild form of West Nile virus have a fever for 5 days, a headache for 10 days, and feel tired for more than a month.
More severe infections involving the brain and spinal cord may cause: headache, high fever, stiff neck, disorientation, reduced attention to surroundings, tremors and convulsions, muscle weakness and paralysis and coma. People with these symptoms should seek medical treatment. Medical treatment involves supportive therapy such as intravenous fluids if a person has experienced prolonged nausea, vomiting and diarrhea, pain relievers, ventilator support as required, and treatment for the prevention of secondary infections.
In most cases your doctor won’t test for West Nile virus unless you have symptoms of meningitis or encephalitis. Then your doctor will test your blood for antibodies to the virus. If you have these antibodies in your blood, your doctor will know that you have West Nile
Personal protection during the months of August and September includes staying indoors between dusk and dawn when mosquitoes are most active, wearing protective clothing when outdoors (i.e., long sleeves and pants with socks and shoes), and using mosquito repellents. The most effective mosquito repellent for use on skin is N,N-diethyl-m-toluamide (DEET). See http://www.hc-sc.gc.ca/hl-vs/iyh-vsv/life-vie/insect-eng.php for more information on insect repellents.
Removal of standing water in barrels, buckets, gutters and flowerpots, which can be used as breeding sites, also helps to reduce the mosquito population.
1. UpToDate - Clinical manifestations and diagnosis of West Nile virus infection
2. Canadian Pharmacist Letter 2003; 19(5): 190520
It is available in concentrations ranging from less than 10 percent to more than 75 percent. The effectiveness of DEET plateaus at approximately 30 percent, but higher concentrations provide longer duration of protection. Products with concentrations around 10% are effective against mosquitoes for periods of approximately three hours; a concentration of about 30% percent provides an average of six hours of protection from mosquitoes. Protection is shortened by swimming, washing, rainfall, sweating, and wiping.
For children aged six months to two years, use 10% concentrations applied no more than once daily. Children aged two to 12 can use 10% DEET applied up to three times daily. Adults and children over 12 years of age can use up to 30% concentrations of DEET and reapply if being bitten by mosquitoes, always follow product instructions. Higher concentrations should be reserved for situations in which insect infestation is high, elevated temperatures and humidity may limit evaporation, or time outdoors will exceed three to four hours.
Do not use insect repellents containing DEET on infants under six months of age. Use a mosquito net when the child is outdoors in a crib, playpen or stroller.
Guidelines for using insect repellents:
• Use enough repellent to cover exposed skin or clothing. Don’t apply repellent to skin that is under clothing. Heavy application is not necessary to achieve protection.
• Do not apply repellent to cuts, wounds, or irritated skin.
• After returning indoors, wash treated skin with soap and water. (This may vary depending on the product. Check the label.)
• Do not spray aerosol or pump products in enclosed areas.
• Do not spray aerosol or pump products directly to your face. Spray your hands and then rub them carefully over the face, avoiding eyes and mouth.
• When using repellent on a child, apply it to your own hands and then rub them on your child. Avoid children’s eyes and mouth and use it sparingly around their ears.
• Do not apply repellent to children’s hands. (Children may tend to put their hands in their mouths.)
• Do not allow young children to apply insect repellent to themselves; have an adult do it for them.
Other ways to protect your children against mosquitoes are to have them wear long pants, long sleeved shirts and closed shoes if they are outside when mosquitoes are active. Mosquitoes are most active at dawn and dusk.Wear light-colored clothing, which will help reduce overall attractiveness to mosquitoes.
In comparison trials, DEET is more effective than any other insect repellent. DEET repels mosquitoes for a longer duration than for ticks. When seeking protection against ticks, look for a product that specifies use for ticks.
4.Pediatr.Ann. 2004 Jul;33(7):443-53 “Does Anything Beat DEET” PMID: 15298309
5.UpToDate - Prevention of arthropod and insect bites: Repellents and other measures
Q. I sat on a high backed chair 2 days ago, just after someone with lice sat on it. Should I use the lice shampoo just in case some lice got on me?
The diagnosis of head lice is definite only when crawling lice are seen in the scalp or hair. Detection is difficult since head lice move quickly and most infections involve 10 or fewer lice. Using a fine–toothed nit comb is four times as effective, and twice as fast as visual inspection for the detection of live head lice. The lice are detected by a thorough combing-through of wet hair from the scalp with the fine-tooth detection comb; lice are usually found at the back of the head or behind the ears. Nits are oval, grayish white eggs fixed to the base of hair shafts. Each adult female louse lays 3 to 5 eggs/day, so nits typically vastly outnumber lice and are not a measure of severity of infection. Some people with a lice infestation may not have any symptoms, but the most common symptom people experience is itching of the scalp, neck and ears.
Only persons with live crawling lice should be treated. Close contacts and household members of someone with lice should be screened for lice. Preventative treatment is unnecessary and may contribute to resistance.
If the diagnosis is positive for lice, all topical lice treatments are available as non-prescription products at pharmacies. The product must be reapplied 7 to 10 days following initial treatment.
2.www.pharmacygateway.ca CE Online CCCEP file # 671-1207 “Head Lice Treatment: Is it time for a paradigm shift?” by Penny Miller, B.Sc.(Pharm.), M.A. March 2008
Bottles of sunscreen shouldn’t last very long if they are being used correctly. To achieve the labelled SPF value a person should apply 2 tablespoons of sunscreen for the full body. The following body parts should have ½ teaspoon each: the face and neck, each arm and shoulder, front of torso, and back of torso. Plus, one teaspoon should be applied to each leg/top of foot. Sunscreen sprays should be sprayed on and rubbed in to ensure uniform coverage.
Apply sunscreen at least 15 to 30 minutes prior to sun exposure and reapply every 2 hours even on cloudy days and after swimming, heavy sweating and towelling off.
For maximum protection from sunburn, skin wrinkling, skin aging and cancer causing UV radiation from the sun use an SPF of at least 15 ( some organizations recommend nothing less than 30 ) on exposed skin every day. You may need a higher SPF if you are fair skinned or plan to be in the sun for a prolonged period or if you anticipate intense sun exposure (eg, while at the beach or skiing ). Snow reflects up to 80 per cent of the sun’s rays, giving you a double dose of radiation when involved in winter sports. Also, use a sunscreen that protects against UVA and UVB radiation.
Other measures that can be used to protect yourself from the sun are to avoid the sun between 10am and 4pm, wear protective clothing like a wide brimmed hat, sunglasses and long sleeves. Protect your lips with lip balm containing an SPF of 30 or higher and re-apply frequently.
1. Sunscreens: achieving optimal protection. Pharmacist’s Letter/Prescriber’s Letter 2009;25(6):250606
2. UpToDate- Patient Information: Sunburn Prevention
The American Diabetes Association recommends the use of aspirin (75 mg to 162 mg per day) as a primary prevention strategy in patients with diabetes who are at increased cardiovascular risk. The Canadian Diabetes Association released their Clinical Practice Guidelines for the Prevention and Management of Diabetes in Canada in September 2008. The recommendation states that use of daily aspirin (81 mg to 325 mg) should be based on clinical judgement.
The use of enteric-coated aspirin is not recommended for reducing the risk of gastrointestinal bleeding or dyspepsia. People at high risk of gastrointestinal bleeding or those with dyspepsia caused by antiplatelet treatment should consider measures to protect the stomach ( for example a proton pump inhibitor ). Aspirin should be taken after food to reduce the risk of gastrointestinal adverse effects. A person should seek medical advice if they experience wheezing or dyspepsia symptoms with low dose aspirin.
Although the optimal dose of aspirin is uncertain, there is no compelling evidence that any specific dose is more effective than another, and fewer gastrointestinal side effects and bleeding occur with lower doses (≤ 325 mg a day). We recommend a dose of 50 to 100 mg daily when using aspirin for the secondary prevention of stroke.
2. Canadian Pharmacist’s Letter
4. UpToDate – Antiplatelet Therapy for Secondary Prevention of Stroke
immunity within 10 days with just one dose.
- people who have had a previous anaphylactic ( severe allergic reaction ) to any element of the vaccine , or people with a hypersensitivity to eggs ( eg. hives, swelling of the mouth and /or throat, breathing difficulty )
- people experiencing a high fever
- people who have previously experienced Guillan-Barre Syndrome within 8 weeks of receiving a seasonal flu vaccine
- the H1N1 flu vaccine is not approved for children under 6 month
People on immunosuppressive medications (e.g. high dose prednisone, cancer chemotherapy, anti-rejection drugs, etc.) may not mount a full immune response after being vaccinated, but vaccination is especially important for these people because
their weakened immune system makes them more susceptible to contracting the H1N1 virus.
Getting the H1N1 flu vaccine is the best way for you to protect yourself
and others from getting infected.
Other common symptoms are sore throat, nasal discharge, fatigue, muscle and joint pains, headache and decreased appetite. Sometimes the person may have vomiting, diarrhea and nausea. Is the pandemic H1N1 2009 virus known to be circulating in your
community? You can check at www.phac-aspc.gc.ca/fluwatch/index-eng.php. Indications that you have a severe case and should seek medical help are shortness of breath, chest pain, dizziness, confusion and/or a high fever lasting longer than 3 days.
Q. If I want to stop taking my sleeping pills can I stop all of a sudden or should I go off of them gradually?
After tapering the medication plan to stop the medication at a low-stress time, e.g., a weekend. Two nights before the planned withdrawal, the patient should shorten the sleep time (while staying on the medication) by 20 minutes. This modest degree of sleep deprivation will promote physiological sleepiness, which should counterbalance any sleep disruption associated with withdrawal. This shortened sleep period should be maintained for one week.
To achieve a good sleep it is important to follow these guidelines referred to as sleep hygiene
1. Keep a regular sleep wake schedule, 7 days per week.
2. Restrict the sleep period to the average sleep time you have obtained each night over the preceding week.
3. Avoid sleeping in, extensive periods of horizontal rest or daytime napping; these activities usually affect the subsequent night of sleep.
4. Get regular exercise every day- about 40 minutes of an activity with sufficient intensity to cause sweating. If evening exercise prevents sleep, schedule the exercise earlier in the day.
5. Avoid caffeine, nicotine, alcohol and other recreational drugs, all of which disturb sleep. If you must smoke do not do so after 7:00 p.m.
6. Plan a quiet period before lights out; a warm bath may be helpful.
7. Avoid large meals late in the evening; a light carbohydrate snack (e.g., crackers and warm milk) before bedtime can be helpful.
8. Turn the clock face away and always use the alarm. Looking at the clock time on awakening can cause emotional arousal (performance anxiety or anger) that prevents return to sleep.
9. As much as possible, keep the bedroom dark and soundproofed. If you live in a noisy area, consider ear plugs.
10. Use the bedroom only for sleep and intimacy; using the bed as a reading place, office or media centre conditions you to be alert in a place that should be associated with quiet and sleep. If you awaken during the night and are wide awake, get up, leave the bedroom and do something quiet until you feel drowsy-tired, then return to bed.
Note: Pharmacologic (or any) interventions will be less effective if these guidelines are not followed. In mild cases of insomnia, sleep hygiene guidelines, practised consistently and together, may be sufficient to reinstate a normal sleep pattern.
2. N. Engl J. Med.2005;353(26):2827
Zostavax reduces the risk of reactivation of the varicella zoster virus, the same one that causes chicken pox. The shingles vaccine contains about 14 times the amount of weakened chicken pox virus than the vaccine for children. This amount is needed to obtain a protective response in the aging immune system of older adults. Anyone who has had chicken pox is at risk of developing shingles. It most commonly occurs in people over 60 and the risk increases as people age. The virus that has been dormant in the nerve cells, once reactivated, travels from the nerves and follows a path out to the skin. The nerves along the path become inflamed and therefore shingles can be painful. Pain that lasts for months after the rash has healed is called post herpetic neuralgia.
The vaccine is safe and common side effects include: headache, pain, swelling, and itching at the injection site. A small group of recipients also got a rash at the injection site.
A single dose of shingles vaccine is indicated for adults 60 years of age and older to prevent the development of shingles.
Q. Can I take my birth control pill continuously? In other words can I skip the 7 days of inactive sugar pills and start taking another pack instead? Im going on a trip and I want to avoid my period.
Guilbert E, Boroditsky R, Black A, Kives S, Leboeuf M, Mirosh M, Senikas V, Wagner MS, Weir E, York-Lowry J, Reid R, Trussell J; Society of Obstetricians and Gynaecologists of Canada. Canadian Consensus Guideline on Continuous and Extended Hormaonal Contraception, 2007. J Obstet Gynaecol Can. 2007 Jul;29(7 Suppl 2):S1-32.
Stockley's Drug Interactions 8th Edition
Only use forearm testing before a meal, an insulin dose, or physical exercise, or 2 hours after a meal, an insulin dose, or exercise.
When blood sugar is changing rapidly, for instance, within 2 hours after a meal, an insulin dose or physical exercise, a forearm blood sample will not show this change as quickly as a fingertip sample.
When blood sugar is falling, testing with a fingertip may identify a hypoglycaemic (low blood sugar) level sooner than a test with a forearm sample.
You should use fingertip testing whenever you have a concern about hypoglycemia (insulin reactions), such as when you drive a car, particularly if you suffer from hypoglycemic unawareness (lack of symptoms to indicate an insulin reaction), since forearm testing may fail to detect hypoglycemia. If the results from the forearm do not match how you feel (high or low), test from the fingertip and use those results.
If you want to use an alternate site because of fingertip pain, please see these tips regarding fingertip pain:
Here are some tips on alternate site blood sugar testing.
For best results from alternate site
testing, individuals should be trained in
proper technique, as follows:
1. The selected alternate site should be
relatively free of hair and cleaned with
soap and warm water.
2. Rub the area vigorously for 5 seconds.
3. The correct end cap to the lancing
device must be used. This is a clear
end cap to allow the user to see the
blood drop form.
4. Press the clear end cap firmly against
the skin for 1 to 2 seconds to help pool
5. Release the lancing mechanism and
leave the end cap pressed firmly
against the skin until the blood drop
forms. If necessary, pressure against
the skin may be released slightly and
reapplied to help the blood drop form.
6. Take the strip to the drop allowing the
capillary action to draw in the sample.
7. Make note in a logbook of which alternate
site has been used.
However, a recent analysis of the existing evidence indicates otherwise. Currently cinnamon has not been found effective in people with type 1 or type 2 diabetes in improving fasting blood glucose, hemoglobin A1C, or lipid levels. Further research is required regarding the use of cinnamon in preventing diabetes in high risk individuals or those with pre-diabetes.
Currently a study is being conducted in Toronto to assess the impact cinnamon has on fasting blood glucose, insulin, glycosylated hemoglobin (HA1C), triglyceride, total cholesterol, HDL cholesterol and LDL cholesterol levels in people with type 2 diabetes. The results of this study will be able to provide more conclusive evidence regarding the use of cinnamon in type 2 diabetics.
Natural Medicines Comprehensive Database 2008: Cassia Cinnamon
Baker WL. Gutierrez-Williams G. White CM. Kluger J. Coleman CI. Effect of cinnamon on glucose control and lipid parameters. [Journal Article. Meta-Analysis] Diabetes Care. 31(1):41-3, 2008 Jan.
Q. I would like to give my infant Tylenol drops for fever caused by recent immunizations but I am worried given that some Tylenol products have been recalled?
Black Cohosh is an herbal product that may also be tried although there is conflicting evidence about how effective it might be. Some trials show that it is no more effective than placebo pills (1) and others show it is more effective than estrogen or placebo (1). That being said, Black Cohosh is relatively safe, with the most common adverse effect being stomach upset (1). There is some concern of liver toxicity and safety beyond six months is not established (1) therefore liver function tests should be monitored periodically. Jaundice, unusual fatigue and dark urine are symptoms of liver toxicity and should they occur should be reported to your doctor (3).
The North American Menopause Society recommends lifestyle modifications with or without non-prescription therapy (including Black Cohosh) for women who need relief of mild menopausal symptoms such as hot flashes (1).
1. Menopause, Vol. 11, 16 No. 1, 2004
2. eTherapeutics April 2007 Menopause
3. Canadian Pharmacist's Letter 2004 (7):200714
Q. I am taking homeopathic products and was wondering if it will interact with my medications?
1. Am J Pharm Educ. 2007 February 15; 71 (1): 07
2. Br J Clin Pharmacol 2007 Sep 15
Q. My baby is crying, screaming and turning red in the face when she "poops". I think she is constipated, what can I give her?
1. Up to Date 2007: Constipation in Children: Etiology and Diagnosis
2. Paul Hyman, M.D. Accessed Aug 28, 2007. " Childhood Defecation Disorders: Constipation and Soiling." http://www2.kumc.edu/kupedigi/Defecation.htm
3. J Pediatr Gastroenterol Nutr. 1999 Nov;29(5):612-26.
Q. I am having difficulties coming off my SSRI antidepressant. Is this normal? What can be done?
The cause of discontinuation symptoms is not completely understood but is thought to result from a temporary deficiency of serotonin in the brain and a temporary deficiency (down-regulation) of serotonin receptors. It may take a couple of weeks for the serotonin and receptors to normalize and discontinuation symptoms to disappear.
Given the proposed mechanism of discontinuation symptoms it is best to reduce the dose of an antidepressant slowly over time rather than to quit taking them outright. There is no clear cut or "best" way to taper an antidepressant. With the exception of Prozac (fluoxetine) most newer antidepressants should be discontinued over several weeks with dose adjustments every 7 days. If withdrawal symptoms occur during tapering, the drug can be restarted and tapered more slowly. Another option is to substitute the drug with Prozac(fluoxetine) which, because of it's long half life, has a "built-in" tapering effect.
1. American Family Physician Volume 74, Number 3.
Q. A friend heard on Canada AM that Fosamax should be discontinued. Is this true? I've had no problems with it. I heard that Fosamax can cause jaw and heart problems and I should stop taking it, is this true?
Fosamax has also been in the news recently with links to irregular heart beats (arrythmias). Two papers published in the New England Journal of medicine showed an increase in serious arrythmias in those taking Reclast, a once yearly injectable bisphosphonate, and the oral form of Fosamax. Again the risk of Fosamax causing serious arrhythmias appears to be very small and may not be significant. In one trial the risk of serious arrhythmia was 1.5% in those taking Fosamax compared to 1% for those not taking fosamax. At this point the risk seems higher with Reclast. As with osteonecrosis of the jaw, most of the time, the benefits of Fosamax therapy outweigh the very small risk of serious arrhythmias.