For those who haven’t been paying attention — either in life generally or to new reporting on Tylenol regarding the potential dangers of acetaminophen — it’s time to snap to. Because I’m sure I’m not the only one reading the new report about children dying from Tylenol overdoses to feel like I’ve been a bit out of the loop on acetaminophen. And in this scenario, confusion can lead to accidental overdoses. [More]
At the intersection of bad marketing, inept regulation, and unwitting consumers, you’ll find the graves of young children, just some of the infants who, according to a new report from ProPublica, have become ill over the decades because Johnson & Johnson and other makers of acetaminophen-based painkillers insisted on selling two youth-targeted varieties of the drug while the FDA did what it does best — nothing. [More]
Johnson & Johnson has revealed a new bottle cap design for Tylenol products sold in the U.S. which will warn consumers in bright red lettering that the medication contains acetaminophen. The labels will alert users to the potentially fatal risks of taking too much Tylenol, which is an unusual step for a company to make. [More]
Because no weekend can get started without news of a possible scary drug interaction, the FDA has issued a consumer alert warning that, in extremely rare cases, use of the popular over-the-counter painkiller acetaminophen (used in Tylenol and many others) can cause “rare but serious skin reactions,” including three serious skin diseases with symptoms like rash, blisters and widespread damage to the surface of skin. Yuck. [More]
Over-the-counter painkillers seem harmless enough, but like any drug, they can cause plenty of pain of their own if overused. According to a study, popping too much acetaminophen over an extended period of time could cause liver failure and possibly lead to death. [More]
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]
19-year old Eva Uhlin has regrown her face, chest, arms, back and stomach. A rare reaction to a couple pills of pain reliever acetaminophen, the main ingredient in Tylenol, caused her to develop Toxic Epidermal Necrolysis, and large parts of her skin turned black and fell off. [More]
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.
“Non-prescription pain relievers used by millions of U.S. consumers need stronger health warnings regarding liver or stomach risk, the Food and Drug Administration said Tuesday.” The drugs in questions are acetaminophen (Tylenol), and NSAIDs like ibuprofen (Advil, Motrin). In particular acetaminophen is associated with liver problems.