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Did you (or a loved one) take Zantac for at least 6 months?

Was the person who took Zantac diagnosed with any of these cancers?

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Widely Used Heartburn Medication Recalled Due to Cancer Risks

Zantac Recalled by FDA Due to Elevated Levels of Potential Carcinogen Nitrosodimethylamine (NDMA)

Zantac neglected to inform the general population regarding the presence of this compound within their product, prioritizing financial gain over the well-being of consumers.

While the FDA sets a permissible daily intake of 96 nanograms of NDMA, analytical assessments divulged that each tablet harbored an excess of 3,000,000 nanograms. This staggering quantity is an overabundance of 3,000 times the FDA's established intake threshold.

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Kidney cancer emerges due to mutations occurring within the DNA of kidney cells. The exact triggers for these genetic changes remain elusive to medical professionals and researchers.

However, specific well-identified risk factors are recognized. Among medications, Nexium, Prilosec, Pepcid, and Tums fall into the category of high-tolerance drugs. The vast majority of individuals usually experience no negative consequences when taking these medications.

Zantac (ranitidine)

Zantac (ranitidine) is employed for addressing heartburn, acid indigestion, GERD, and gastric ulcers. It pertains to a category of medications known as H2 blockers. A recall was initiated by the FDA following the discovery that Zantac formulated with ranitidine contained the carcinogenic compound NDMA.
The precise catalysts behind these genetic alterations remain uncertain to doctors and researchers. Nevertheless, certain recognized risk factors exist. Nexium, Prilosec, Pepcid.

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