Drugmakers may be recalling the heartburn med Zantac around the world, but the FDA wants consumers to stop worrying. Higher-than-recommended levels of a possible carcinogen in the pills are no more dangerous than a grilled ribeye, the agency said Monday.
Testing of recalled lots of branded and generic Zantac showed levels of a contaminant known as N-Nitrosodimethylamine (NDMA) that were as much as nine times greater than the FDA’s recommended limit
––but the agency pooh-pooh’d the health risk in a release.
Janet Woodcock, director of the FDA’s Center for Drug Evaluation and Research, said despite NDMA levels that were at times significantly above the acceptable limits, the amount of the compound found in the drugs was comparable to levels found in “grilled or smoked meats.” Moreover, the FDA concluded that consuming Zantac didn’t cause NDMA to form in the stomachs of patients, as had been previously posited.
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“We understand the concern we’ve been hearing from parents and pediatricians, and we’ll continue to investigate,” Woodcock said.
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