Zantac Cancer Claim Information


On September 13, 2019 the Food & Drug Administration (FDA) issued a public warning concerning Zantac and other similar ranitidine medicines (generics). The FDA reports that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac®, contain a nitrosamine impurity called nitrosodimethylamine (NDMA).

NDMA (the contaminant identified in Zantac) is classified as a probable human carcinogen which means that it is more likely than not to cause cancer in humans. Recent studies have raised the specter of an association between NDMA and liver toxicity which can lead to the development of liver cancer and other related conditions brought about by an NDMA-induced “insult” to the liver.

Cancers that are linked to NDMA exposure include: Liver Cancer, Colorectal Cancer, Intestinal Cancer, Colon Cancer, Stomach Cancer and Kidney Cancer (Renal Cancer). Other possibly related cancers include: Lung Cancer, Pancreatic Cancer, Ovarian Cancer, Testicular Cancer and Esophageal Cancer. 

BRW Injury Lawyers are investigating these claims. If you or a loved one developed any of the above cancers after using Zantac (or other ranitidine medication) for a few months, you may have a claim. For more information call BRW Injury Lawyers at 251 433-7766 or email BRW:    Please share this important information.

ZANTAC is a registered trademark of Warner-Lambert Company, used under license. In the United States, 75- and 150-mg tablets are available OTC. Zantac OTC is manufactured by Sanofi Consumer Healthcare.

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