Tuesday, June 16, 2009

FDA urges consumers to stop using Zicam due to loss of sense of smell

The U.S. Food and Drug Administration advised consumer to stop using three Zicam products marketed over-the-counter as cold remedies because they are associated wtih the loss of sense of smell (anosmia) on June 16th.

The products are:
--Zicam Cold Remedy Nasal Gel
--Zicam Cold Remedy Nasal Swabs
--Zicam Cold Remedy Swabs, Kids Size (a discontinued product)

More than 130 reports of loss of sense of smell associated with the use of these three Zicam products were reported to the FDA. Many people who experienced a loss of smell said the condition occurred with the first dose; others reported a loss of the sense of smell after multiple uses of the products.

“Loss of sense of smell is a serious risk for people who use these products for relief from cold symptoms,” said Janet Woodcock, M.D., director of the FDA’s Center for Drug Evaluation and Research (CDER). “We are concerned that consumers may unknowingly use a product that could cause serious harm, and therefore we are advising them not to use these products for any reason.”

People who have experienced a loss of sense of smell or other problems after use of the affected Zicam products should contact their health care professional. The loss of sense of smell can adversely affect a person’s quality of life, and can limit the ability to detect the smell of gas or smoke or other signs of danger in the environment.

The FDA has issued Matrixx Initiatives, maker of these Zicam products, a warning letter telling it that these products cannot be marketed without FDA approval.

See the FDA website links below for more information on Zicam :
http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm166931.htm


NIH provides information about homeopathy: http://nccam.nih.gov/health/homeopathy/