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It became particularly useful for the treatment of gastroesophageal reflux disease (GERD). When someone has GERD, they experience acid reflux that can damage the tissue of the esophagus.

Public service announcements, physician education, celebrity media tours, and consumer-awareness bulletins were used by the pharmaceutical company to skyrocket its medication to success. Pfizer gained FDA approval to sell over-the-counter versions of Zantac in the United States. This event led to a deal with Sanofi SA, the company that currently sells Zantac in the United States. Valisure alerted the FDA about the concerning amount of NDMA it found in ranitidine products. The discovery caused the agency to alert the American public but take no official action.

The FDA cited a lack of research existing to issue a recall. Just days after news about NDMA impurities broke, Novartis AG stopped distributing its generic versions of Zantac.

On the same day, Canada requested all ranitidine producers to stop distributing their products. By the end of September, major American retailers such as CVS, Walgreens, and Rite Aid had pulled their ranitidine products from shelves.

While it did not initiate a recall, it advised companies to stop selling the drug. At this point, many countries had banned the sales of ranitidine products.

The FDA cited the need for more testing to explain its slow response when compared to other nations. By the end of October, many Zantac and ranitidine producers stopped distributing their products or recalled them.

Finally, after months of testing, the FDA released an official request for all Zantac and ranitidine products to stop being sold in the United States. It also informed those that took the medication to stop doing so and find an alternate drug. It also found that their NDMA level could increase the longer they are kept on a shelf, even at normal room temperatures.

This means that some ranitidine products could become increasingly carcinogenic the longer they are on store shelves. Our attorneys are ready to fight for losses associated with your cancer including medical bills, lost wages, and pain and suffering.

September 2019Valisure alerted the FDA about the concerning amount of NDMA it found in ranitidine products. April 2020Finally, after months of testing, the FDA released an official request for all Zantac and ranitidine products to stop being sold in the United States.

Categories Injury, Product Liability Suggested Posts Common Dangerous Vehicle Defects Does FDA Approval Mean a Product Is Safe. Why Is Roundup Still Being Sold. Last Name: Please enter your last name.

Email: This isn't a valid email address. Phone: This isn't a valid phone number. Please enter your phone number. Yes, I am a potential new client. No, I am a current, existing client. Are You a New Client. Please make a selection. Tell Us About What Happened: Please enter a message. These listings are not a guarantee or prediction of the outcome of any other claims. It follows concern in several countries over the presence of impurities in Zantac and other ranitidine products.

Canada and France have already announced Zantac recalls. The US and the European Union are investigating. Health authorities say there is no immediate risk, but patients have been advised to consult a doctor who can prescribe alternatives to ranitidine.

On 13 September, both the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) published their decisions to review the presence of N-nitrosodimethylamine (NDMA) in medicines containing the drug ranitidine.

NDMA is classified as a probable human carcinogen (a substance that could cause cancer) on the basis of animal studies. NDMA is found in water and foods, including meats, dairy products, and vegetables, but is not expected to cause harm when ingested in very low levels, EMA says. Ranitidine products are used to reduce the production of stomach acid in patients with conditions such as heartburn and stomach ulcers.

CVS's announcement on Saturday said it was suspending the sale of Zantac and CVS Health brand ranitidine products "out of an abundance of caution". Walgreens, Walmart and Rite Aid in the US had earlier taken a similar decision.

Canada and France have removed the drugs from pharmacy shelves. A number of other countries have followed suit. Bangladesh on Sunday issued a temporary ban on the import, production and sale of ranitidine while it investigates the links to cancer.

Sandoz, owned by Novartis, told the BBC it was recalling "several batches of its ranitidine-containing medicines". The recalls were "under way or pending" in Australia, Austria, Belgium, Canada, Croatia, the Czech Republic, Denmark, Finland, Germany, Hungary, North Macedonia, Portugal, Slovakia, Slovenia, Sweden, Switzerland and the US. Apotex also said it was recalling ranitidine tablets in the US. The BBC has approached GlaxoSmithKline - original makers of Zantac.

The company is reported to have stopped distributing its generic version of the drug and recalled its products from India and Hong Kong. Health regulators are urging people taking ranitidine not to discontinue it immediately. The FDA said, however, that those taking it by prescription should contact health professionals about alternatives. And those buying it over the counter could consider other options. French authorities also emphasised there was no "acute risk" and patients should not stop the medication or return it to pharmacies.

Heartburn 'could be sign of cancer'US Haiti envoy quits over 'inhumane' deportationsDaniel Foote says US policy on Haiti is "flawed" and sending migrants back is "counterproductive".

What is the fear about. They are available over-the-counter and on prescription. Who has recalled the products so far. Drug makers are also recalling products containing NDMA. What should patients do. Related TopicsCanadaCancerFranceUnited StatesPrescription drugsMore on this storyHeartburn 'could be sign of cancer'Published26 January 2015Top StoriesUS Haiti envoy quits over 'inhumane' deportationsDaniel Foote says US policy on Haiti is "flawed" and sending migrants back is "counterproductive".

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The medication is known as Zantac and is sold over the counter and by prescription. According to the FDA, Zantac contains 26,000 times more of that impurity than the FDA allows. What Is The Cancer-Causing Ingredient In Zantac.


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