FDA issues recall for Zantac after confirming the medication can breakdown to create NDMA a known carcinogen. On April 1st, 2020 the FDA issues the following statement. "The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine (NDMA) in ranitidine medications (commonly kn
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FDA issues recall for Zantac after confirming the medication can breakdown to create NDMA a known carcinogen. On April 1st, 2020 the FDA issues the following statement. "The
Lawsuit Watch. . FDA issues recall for Zantac after confirming the medication can breakdown to create NDMA a known carcinogen. On April 1st, 2020 the FDA issues the following statement. "The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from ...
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FDA finds cancer-causing chemical in heartburn medicine Zantac
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Via America’s Lawyer: 15 million Americans suffer from heartburn and have turned to Zantac as a popular relief aid. But the FDA recalled the drug last year, and a class-action lawsuit against manufacturers is on the horizon. From the Mass Torts Made Perfect conference in Las Vegas, attorney Madeline Pendley joined RT’s Brent Jabbour, filling in for Mike Papantonio, to explain how the makers of Zantac have spent decades sweeping serious cancer risks under the rug. Find out more about Zantac lawsu
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798K views · 970 reactions | Recent studies have raised concern after showing Zantac may react with itself to form a cancer causing compound known as NDMA. | Lawsuit Watch | Facebook
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