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Mesothelioma company. After valisures petition the fda conducted its own testing of ranitidine drugs. Food and drug administration fda of the presence of a cancer causing chemical in certain batches of zantac and its generic ranitidine in 2019. For example several major retailers removed the prescription and over the counter formulas of zantac from their shelves.
The issue of whether ranitidine commonly known as zantac causes levels of the probable carcinogen n nitrosodimethylamine ndma to rise in users bodies has been raised previously by valisure an online pharmacy that originally flagged the potential contamination of ranitidine to the fda. This followed an initial notification provided to the fda in june 2019. In september 2019 valisure filed a citizen petition requesting that the fda recall all ranitidine products in the united states based on their findings.
Be sure to announce it so everybody knows and gets excited. Having a big sale on site celebrity or other event. Valisures discovery sparked waved of changes.
The online analytical pharmacy valisure advised the us. Personal injury mesothelioma cancer mesothelioma cancer. Because valisure tests batches of the drugs it sells the company petitioned the fda to recall ranitidine drugs conduct examinations about their safety and.
More than 3500 people are diagnosed with mesothelioma each year in the u. Valisures lab testing found some zantac formulas contain more than 3000000 ng per tablet.
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