DID ZANTAC CAUSE YOUR CANCER?
YOU MAY BE ENTITLED TO COMPENSATION

The FDA has requested removal of all Ranitidine products (Zantac) from the market, as it may cause cancer and
other serious injuries!

See If You Or A Loved One Qualify For Potential Compensation

Where you or a loved one diagnosed with cancer after taking Zantac?

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HAVE YOU TAKEN ZANTAC AND SUFFERED FROM?…

Bladder Cancer
Breast Cancer
Colon Cancer
Esophageal Cancer
Kidney Cancer
Liver Cancer
Melanoma
Ovarian Cancer
Prostate Cancer
Stomach Cancer

IT’S TIME FOR THESE COMPANIES TO TAKE RESPONSIBILITY

The International Agency for Research on Cancer (IARC) and the World Health Organization have stated that NDMA is “probably carcinogenic to humans.” Due to the toxic nature of NDMA, the FDA advises people not to consume more than 96 nanograms of NDMA a day. Previous testing found that there are more than 3,000,000 ng in one

Zantac pill. Zantac’s manufacturers, including Sanofi, had the obligation to warn users of the drug’s possibly harmful side effects, but waited until after the FDA conducted research and released advisories about Zantac’s health risks. Hold companies like Sanofi accountable for marketing a product that contains a cancer-causing chemical.

The FDA recommends avoiding products with more than 96 nanograms of NDMA per day. Zantac has been shown to have more than…

 

3 MILLIONng
IN EVERY
ZANTAC
PILL!

INJURY REVIEW CAN HELP GET THE COMPENSATION YOU’RE ENTITLED TO TODAY!

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