FDA's MedWatch Safety Alerts: December 2009

FDA's MedWatch Safety Alerts: December 2009

On this page:

-Recall: Tylenol Arthritis Pain Caplet, 100 Count Bottles
-Birth Defects Related to Depakote and Similar Drugs
-Recall: Sexual Enhancement Products from Atlas Operations
-Recall: Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels
-Recall: Thermoflect Products
-Voltaren Gel and Liver Damage
After the Food and Drug Administration (FDA) approves a product and it is on the market, FDA continues to monitor unexpected and undesirable side effects (adverse events) of that product.

Health care professionals and consumers may report side effects, product quality problems, product use errors, or therapeutic failure with the use of medical products to FDA's MedWatch Adverse Event Reporting program either online, by regular mail, by fax, or by phone.

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FDA's MedWatch Safety Alerts: December 2009