Zantac Heartburn Drug May Contain Carcinogen: FDA

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Zantac Heartburn Drug May Contain Carcinogen: FDA
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🚨 CONSUMER ALERT 🚨: The FDA reports that a substance that could cause cancer has been found in some ranitidine heartburn and ulcer medicines, including the brand-name drug Zantac.

Patients who are taking prescription ranitidine and want to stop using it should discuss alternatives with their health care provider, the FDA advised. Those taking over-the-counter ranitidine could switch to other OTC medicines.NDMA is an environmental contaminant found in water and foods, including meats, dairy products and vegetables. It is classified as a probable human carcinogen.

The FDA said it's evaluating whether the low levels of NDMA in ranitidine pose a risk to patients and that it will post that information when it's available. In the meantime, Dr. Janet Woodcock, director of the FDA's Center for Drug Evaluation and Research, said the FDA is working with international regulators and industry partners to find out where the contamination originated."The agency is examining levels of NDMA in ranitidine and evaluating any possible risk to patients," she said in a news release."The FDA will take appropriate measures based on the results of the ongoing investigation.

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