Have You Or A Loved One Been Diagnosed With Cancer After Using Zantac®?
HAVE YOU OR A LOVED ONE BEEN DIAGNOSED WITH CANCER AFTER USING ZANTAC®?
• STOMACH CANCER
• BLADDER CANCER
• PANCREATIC CANCER
• LIVER CANCER
• TESTICULAR CANCER
• OTHER CANCERS
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YOU OR A LOVED ONE MAY BE ELIGIBLE FOR A SETTLEMENT
Zantac's® manufacturer, Sanofi®, has issued a recall for its popular heartburn medication after the Food and Drug Administration (FDA) warned that the drug created a cancer-causing carcinogen called NDMA after being consumed by patients.
Multiple follow up studies have confirmed dangerously high levels of NDMA being present. If you or a loved one have taken Zantac® or its generic versions and now suffer from cancer, you may be entitled to compensation.
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Answer a few basic questions in our free online evaluation to see if you qualify
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File Your Claim
We will prepare and file your claim on your behalf at no cost to you
ZANTAC® WAS PRESCRIBED 15 MILLION TIMES PER YEAR. ARE YOU AFFECTED?
The Hidden Dangers Behind Zantac®
Millions of Americans have taken Zantac® (ranitidine) for the treatment of heartburn or acid reflux. However, independent groups have found large traces of NDMA in Zantac® along with its generic versions.
Levels of NDMA found in Zantac® are between 3,000 and 26,000 times higher than the amount deemed safe by the FDA. In response, thousands of pharmacies and local stores have removed Zantac® and its generic versions from their shelves.
Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with ZANTAC®, Sanofi®, a drug manufacturer, or any government agency.
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