FDA Panel Urges Cuts in Acetaminophen Dosage

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Concerns Over Unintentional Overdose Hazards May Change How Drug Is Marketed

By DAN CHILDS
Abc News

An expert panel convened by the U.S. Food and Drug Administration voted today to recommend greater regulation of acetaminophen -- the most commonly used painkiller in the country.

FDA Panel Urges Cuts in Acetaminophen Dosage
An expert panel convened by the U.S. Food and Drug Administration voted today to recommend greater regulation of acetaminophen in response to overdose fears.
(Getty Images)

Specifically, the panel at the Center for Drug Evaluation and Research Joint Meeting of the Drug Safety and Risk Management Advisory Committee, the FDA's Nonprescription Drugs Advisory Committee, and the Anesthetic and Life Support Drugs Advisory Committee has already voted to urge the FDA to switch to prescription status the strongest of the over-the-counter acetaminophen products, which contain a 1,000 mg dose.

The decision affects a variety of popular over the counter products, including the recommended dosage of Extra Strength Tylenol and other Tylenol products. The dosing instructions for Extra Strength Tylenol indicate that adults should take two 500-mg tablets every 4 to 6 hours. Read more...

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