FDA Considering Banning Certain Painkillers Containing Acetaminophen
December 19, 2011
The Food and Drug Administration (FDA) is considering a ban on the two painkillers, Percocet and Vicodin, because of concerns regarding the amount of acetaminophen in the drugs. According to Health Central, acetaminophen is the leading cause of liver failure in the United States today.
The recommendation came to the agency through an advisory committee that examined the links between the amount of acetaminophen patients take and the occurrence of liver failure in those patients. Based on their findings, researchers are recommending that dosages for acetaminophen be lowered from 1,000 mg to 640 mg per tablet. Also, the current daily limit would be lowered form 4,000 mg to 2,600 mg per day. They are also asking the agency to ban painkillers that combine acetaminophen with other painkillers.
Acetaminophen is widely used in both prescription and over-the-counter (OTC) products to reduce pain and fever. It is also one of the most commonly used drugs in the United States. OTC products containing acetaminophen (e.g., Tylenol) are not affected by this action, but information regarding the potential for liver injury is already required on the label for OTC products containing acetaminophen. The FDA is continuing to evaluate ways to reduce the risk of acetaminophen-related liver injury from OTC products.
The Memphis Drug Injury Lawyers with John Michael Bailey would encourage anyone who is taking a medication containing acetaminophen to examine how much you take per day to ensure you are within safety guidelines. If you are taking more than 2,600 mg per day of acetaminophen, it is recommended that you speak with your doctor immediately.
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