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Pharmaceutical Litigation

Serzone®

Serzone
Serzone

Liver Failure Possibly Linked to Serzone®

We are currently evaluating cases involving the potentially harmful effects on the liver caused by the prescription drug Serzone®. Serzone® is a popular anti-depressant medication that is made by Bristol-Myers Squibb Company, Inc. On December 7, 2001, the United States Food and Drug Administration (FDA) informed Bristol-Myers Squibb that it must provide a so-called "black box" warning on its label for Serzone® to advise patients that rare but possibly life-threatening liver failure can occur with use of the drug.

We are currently investigating reports that Bristol-Myers Squibb failed to properly warn users of the known danger that Serzone® could cause life-threatening liver damage or failure.

If you or someone you know has sustained liver failure or liver damage while taking Serzone®, please contact us to discuss your rights, Click Here or call us toll-free at 1-800-305-7552.

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Recall News
DIGITEK RECALL!

The FDA has recalled all Digitek tablets after the discovery of manufacturing defects.  Individuals taking Digitek tablets may suffer from an illness known as Digitalis Toxicity and various other symptoms.  This manufacturing defect may cause serious health problems, and even death.   

Product Recall
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