People who developed cancer after taking ranitidine-based ZANTAC® filed lawsuits following its recall due to potential cancer risks.
The FDA told all manufacturers to stop selling ZANTAC® made with Ranitidine in the United States in April 2020 because NDMA contamination can increase over time. The longer the drug sits on the shelf, the greater the amount of NDMA in the drug and the FDA doesn’t know how long NDMA has been in ZANTAC®.
The main claim in ZANTAC® lawsuits was that defendants failed to warn the public adequately that ZANTAC® active ingredient, ranitidine, is unstable and can form NDMA in the stomach, which in turn leads to an increased risk of cancer. Plaintiffs demand to be compensated for injuries and pain and suffering.
If you or a loved one experienced adverse side effects or complications related to a ZANTAC® usage, you deserve justice. Complete the form TODAY to make sure you have the best chance to get the compensation you deserve.
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