Zantac is being recalled in the U.S. and Canada ‘due to possible contamination’

Zantac is being recalled in the U.S. and Canada ‘due to possible contamination’

Zantac is being recalled in the U.S. and Canada after an investigation found small amounts of a probable human carcinogen in versions of Zantac and its generic version, ranitidine. (Photo: Drew Angerer/Getty Images)

statement on Friday, follows a Sept. 13 announcement by the Food and Drug Administration that low levels of NDMA (N-Nitrosodimethylamine) had been found in ranitidine — a stomach acid-blocking medication sold under the name Zantac. “NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests,” noted the agency.’ data-reactid=”23″>The recall, which drugmaker Sanofi called “precautionary” and “voluntary” in a statement on Friday, follows a Sept. 13 announcement by the Food and Drug Administration that low levels of NDMA (N-Nitrosodimethylamine) had been found in ranitidine — a stomach acid-blocking medication sold under the name Zantac. “NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests,” noted the agency.

In the statement, Sanofi said the Zantac recall stems from “possible contamination.” “Due to inconsistencies in preliminary test results of the active ingredient used in the U.S. and Canadian products, Sanofi has made the decision to conduct the voluntary recall in the U.S. and Canada as the investigation continues,” the statement read, adding, “The company is working with health authorities to determine the level and extent of the recall.”

Walgreens, and Rite Aide halting sales of Zantac “out of an abundance of caution.”’ data-reactid=”26″>The recall comes in the wake of CVS, Walmart, Walgreens, and Rite Aide halting sales of Zantac “out of an abundance of caution.”

statement, the FDA didn’t appear concerned by the amounts of NDMA found in the heartburn medications. Janet Woodcock, MD, director of the FDA’s Center for Drug Evaluation and Research, said: “Although NDMA may cause harm in large amounts, the levels the FDA is finding in ranitidine from preliminary tests barely exceed amounts you might expect to find in common foods.”” data-reactid=”27″>However, in last month’s statement, the FDA didn’t appear concerned by the amounts of NDMA found in the heartburn medications. Janet Woodcock, MD, director of the FDA’s Center for Drug Evaluation and Research, said: “Although NDMA may cause harm in large amounts, the levels the FDA is finding in ranitidine from preliminary tests barely exceed amounts you might expect to find in common foods.”

Benyam Muluneh, a clinical pharmacist practitioner at the University of North Carolina’s Eshelman School of Pharmacy, told Yahoo Lifestyle that there are several other options to help manage symptoms and suggested that people first get in touch with their healthcare providers (or local pharmacist) for recommendations.’ data-reactid=”30″>For those who are concerned about taking their heartburn medications, Benyam Muluneh, a clinical pharmacist practitioner at the University of North Carolina’s Eshelman School of Pharmacy, told Yahoo Lifestyle that there are several other options to help manage symptoms and suggested that people first get in touch with their healthcare providers (or local pharmacist) for recommendations.

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