The distribution decision by Sandoz only recently happened, but people are concerned that ranitidine has been on the market for years. Academics have recently focused on potential sources of NDMA, as the levels of NDMA in wastewater are rising. It is classified as a probable carcinogen --a cancer-causing chemical -- according to the Environmental Protection Agency. “Let me be clear since the FDA is not: This is not even close to Valsartan.”“As we allege in our lawsuit, and we intend to prove, there is a fundamental defect with Zantac: when ingested, it forms a potent carcinogen (NDMA) in your body that exceeds FDA permissible intake limits by thousands of times,” he said. Please talk to your doctor if you have concerns about ranitidine.
“The FDA has become a shell of an agency. The leading theory is that enzymes in the body react with ranitidine to create NDMA. During disasters and emergencies – and even during large-scale national security events - the …
Instead, it seems determined to protect the big pharmaceutical companies by perpetuating the secret these companies have kept from the public for nearly 35 years: that when ingested, Zantac (or generic ranitidine) breaks down into a potent carcinogenic substance inside the body.”“We are not going to sit idly by, while the FDA continues to encourage pregnant mothers who suffer from pregnancy-related heartburn and others to keep taking Zantac, while the FDA continues to dither and spread misinformation presumably in an effort to mask its incompetence,” he added.“Even though the FDA first learned in June 2019 about the possibility that a carcinogen was associated with Zantac, it waited nearly three months before it issued its first piece of disinformation concerning Zantac. In their petition which was shown to ABC News, Valisure, which promises customers they will test each lot of medication before distributing it, proposed the idea that the NDMA was the result of the formulation of the ranitidine molecule, which they think may break down when it is digested in the human body creating NDMA. Providing the best medical care in the worst of times. Its job is to protect the public from harmful drugs.
“If the levels of NDMA is that high, have we missed or not seen the cancer?” asked Dr. Jon Ernstoff, a gastroenterologist and an external consultant for Valisure. Sandoz had agreed to recall its ranitidine products worldwide including in the U.S.“When retailers like Walmart, or pharmaceutical companies like Sanofi are left to police themselves, it is clear that the federal agencies in place to protect the public are failing to do their job,” Berman said. Other medications are equally effective." That has not been done yet,” Ernstoff said in response to concerns about ranitidine, NDMA and cancer. Prior results do not guarantee a similar result. “If the levels of NDMA is that high, have we missed or not seen the cancer?” asked Dr. Jon Ernstoff, a gastroenterologist. As
“The FDA’s handling of this serious health concern is only causing confusion.”If you have concerns about any potential adverse health risks associated with Zantac (or generic ranitidine consumption), Hagens Berman recommends that you discuss the allegations in this lawsuit with your physician.Multiple health regulation groups are now investigating levels of the carcingenic chemical N-nitrosodimethylamine (NDMA) in Zantac/Ranitidine.Hagens Berman Sobol Shapiro LLP is a class-action litigation firm that seeks to protect the rights of consumers, workers, whistleblowers, investors and others.
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