Zantac ® Recalled Due To Cancer Link. Those Affected May Be Eligible For Compensation!

Zantac ® Recalled Due To Cancer Link. Those Affected May Be Eligible For Compensation!



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Compensation May Be Available For Those Affected

Millions of Americans have taken Zantac® (ranitidine) to treat the symptoms of heartburn and acid reflux disease. While Sanofi®, Zantac's® manufacturer, stated that the drug was safe, recent evidence suggests that NDMA (a cancer-causing carcinogen) is released after patients take Zantac®.

Independent laboratories have confirmed that each 150mg Zantac® dose may produce between 2.4 million and 3.2 million nanograms of NDMA, over 3,000x more than the limit set forth by the FDA.

Billions in profits made on unsafe Medication

The Dangers Behind Zantac®

Zantac's® manufacturer, Sanofi®, has recalled it's heartburn medication following an FDA (Food and Drug Administration) warning that the medication created a cancer-causing carcinogen known as NDMA after it was consumed. Follow up studies have confirmed dangerous levels of NDMA being present.

Additionally, several manufacturers of the generic versions of Zantac® have also recalled their products due to NDMA contamination. Both generic and name-brand forms of Zantac® have been found to create NDMA as a by-product in the human body.



As thousands of Americans suffer from cancer development, many are questioning the role Zantac® and its generic ranitidine played in their cancer development, especially for breast cancer and non-Hodgkin's lymphoma patients.

It has widely become speculated that the multi-billion dollar pharmaceutical giant Sanofi® (Zantac's® manufacturer) knew that their drug created a cancer-causing carcinogen once ingested, yet failed to warn the public of this danger.


Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with a Zantac®, Sanofi®, Zantac's® generic manufacturers, or any government agency.


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