
The Dangers of Prescription Painkillers
FDA: discontinue high-dose acetaminophen
The FDA is asking health professionals to discontinue prescribing acetaminophen products that contain over 325 mg per dose. A recent FDA statement reports that there is no data proving that doses over this amount provide any benefit to negate the increased risk. Acetaminophen is often found in prescription drugs taken as pain relievers and is often found in conjunction with other active ingredients.
Acetaminophen can be harmful to the liver in large doses. It has been known to cause ...
continue reading...Johnson & Johnson Announces New Warnings For Extra Strength Tylenol
Risks of Liver Damage and Death Form Basis for Concern
Johnson & Johnson has announced that, beginning in October, bottles of Extra Strength Tylenol sold in the U.S. will be accompanied by new warnings and instructions. The warning will make it explicitly clear that the drug contains acetaminophen, a pain-relieving ingredient that is the nation’s leading cause of sudden liver failure. According to data from the Centers for Disease Control and Prevention and the Food and Drug ...
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Users of Aspirin Replaced With Acetaminophen at Risk for Serious Liver Failure

Tylenol/Acetaminophen MDL Formed to Address Liver Injury Lawsuits

When creating the MDL, the Panel noted ...
continue reading...FDA: Acetaminophen Increases Risk of Stevens-Johnson Syndrome

According to the FDA, SJS and TEN are extremely rare but can be deadly. These conditions can cause blisters, serious rashes, reddening of the skin and the detachment of the upper surface of ...
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