Acetaminophen Drug Injuries Prompt FDA to Issue Dosage Warnings

January 30, 2014

Advancements in the field of medicine has supplied us with the drugs we need to treat a variety of ailments. But some of these medications can have serious side effects when not used properly. The North Carolina Personal Injury Lawyers with HensonFuerst point out the U.S. Food and Drug Administration (FDA) has recently issued a warning regarding drugs containing acetaminophen because of health risks.

The FDA has received numerous reports of Acetaminophen Drug Injuries, including patients who suffered liver damage and dangerous skin reactions. Both of these adverse health events have been directly associated with consuming large doses of the ingredient.

According to an article from CNN News, this discovery has prompted the FDA to call for lower limits on the amount of acetaminophen a patient should consume within each dosage. Officials say doctors should prescribe a patient no more than 325 mg of Acetaminophen per dose. Furthermore, patients should consume no more than 4,000 mg of Acetaminophen per day.

The recommendations only cover prescription medications though, and the FDA says it will address the risk involving over-the-counter drugs at a later time.

The North Carolina drug injury attorneys with HensonFuerst are aware of the devastating effects an Acetaminophen drug injury can have on a victim’s life and encourage anyone who has been harmed by the drug to discuss their legal rights and options with a qualified attorney as soon as possible.

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