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Why Zantac® is off store shelves
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.
Those that took Zantac® and developed cancer are encouraged to come forward and receive a 100% free legal case review.
Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Zantac® or any government agency.
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