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As Tylenol Lawsuits Mount, Bernstein Liebhard LLP Comments on New Analysis Questioning Labeling Standards for Over-The-Counter Acetaminophen Products
Date:8/25/2014

New York, New York (PRWEB) August 25, 2014

As Tylenol lawsuits (http://www.tylenollawsuitclaims.com/) continue to mount in federal court, Bernstein Liebhard LLP notes the publication of a new analysis by Consumer Reports that raises questions about the labeling standards for over-the-counter acetaminophen products. Among other things, Consumer Reports found that because federal health regulators seem to be more focused on prescription painkillers, labeling for over-the-counter medications containing acetaminophen is extremely inconsistent. For example, while some manufacturers set maximum daily dosage at 1,000 mg per day, labeling for other products suggests that up to four times as much can be taken safely. *

“Scores of Tylenol lawsuits are currently pending in U.S. courts that allege the acetaminophen contained in these products caused patients to suffer serious liver injuries. Among other things, plaintiffs claim that Tylenol’s labeling did not provide adequate warnings about the association between acetaminophen and liver damage,” says Bernstein Liebhard LLP, a nationwide law firm representing the victims of defective drugs and medical devices. The Firm is offering free legal reviews to consumers who allegedly suffered acetaminophen-induced liver damage resulting in hospitalization, liver transplantation, or death after ingesting a Tylenol product.*

Tylenol Liver Damage Allegations
Court documents indicate that at least 150 Tylenol lawsuits involving liver damage allegations have been filed in a federal multidistrict litigation underway in U.S. District Court, Eastern District of Pennsylvania. Among other things, the claims allege that individuals who used these medication suffered severe liver damage resulting in hospitalization, liver transplantation, or d
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