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Zantac Lawsuits

A Zantac lawsuit is a legal claim filed by people who developed cancer after taking Zantac and ranitidine tainted with NDMA. Zantac lawsuits seek compensation from the drug makers for cancers of the bladder, stomach, esophagus, liver, and pancreas that may have been caused by NDMA exposure.

Zantac Lawsuit Facts
FAQs

Bladder, gastric/stomach, esophageal, liver and pancreatic

    Sanofi-Aventis U.S. LLC, Sanofi US Services Inc., Chattem, Inc., Boehringer Ingelheim, Pfizer and GlaxoSmithKline

      Initial stages, no trials scheduled

        Who Is Eligible to File a Lawsuit?
        Cancers that qualify for Zantac lawsuits include:
        • Bladder
        • Gastric/Stomach
        • Esophageal
        • Liver
        • Pancreatic

        People must meet several prerequisites, according to Zantac lawyers, in order to be eligible for a lawsuit: documented Zantac use, a cancer diagnosis, and a link between the disease and Zantac. Lawyers are only considering claims from persons who used the brand-name Zantac, and generic ranitidine is no longer covered.

        Only a lawyer can correctly evaluate a claim, as well as assist in the collection of medical documents and data needed to develop a case.

        Diagnosed with cancer after taking Zantac?
        Free Case Review

        According to Zantac lawyers, several doctors who diagnosed persons with cancer after taking Zantac indicated they had no family history or genetic indications for cancer. Instead, doctors told patients that the illness was due to something in their surroundings, such as NDMA poisoning.

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