FDA Asks Prescription Drug Companies To Limit Amount Of Acetaminophen

FDA Asks Prescription Drug Companies To Limit Amount Of Acetaminophen

Worried about the possibility of liver damage from over use, the U.S. Food and Drug Administration has asked manufacturers of prescription drugs containing acetaminophen to limit the amount of acetaminophen to no more than 325 mg in each tablet or capsule. [More]

FDA May Take Vicodin And Percocet Off The Market

FDA May Take Vicodin And Percocet Off The Market

Bad news for Dr. Greg House and other, non-fictional chronic pain patients. The FDA advisory panel that met yesterday about the effects of excessive doses of acetaminophen made another recommendation to the FDA—to take popular painkillers Vicodin and Percocet (and their generic versions) off the market because of the effect both drugs can have on the liver when taken for extended periods. The FDA will most likely follow this recommendation.