Pediatric Testicular Cancer Patient Alert
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Pediatric Testicular Cancer Patient Alert
Certain Medications Linked to Pediatric Testicular Cancer
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YOU OR A LOVED ONE MAY BE ELIGIBLE FOR A SETTLEMENT
Earlier this year, the Food and Drug Administration (FDA) released a statement stating that Zantac® (ranitidine) contains a chemical impurity known as NDMA. This impurity has been classified as a "probable human carcinogen" by the World Health Organization.
If you or a loved one took Zantac® (ranitidine) while pregnant and have a son with testicular cancer, you may be entitled to compensation.
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MILLIONS IN CORPORATE PROFITS BASED ON A DANGEROUS DRUG
The Hidden Dangers Behind Zantac®
For decades, Zantac® and its generic versions were prescribed by physicians to pregnant women who suffered from pregnancy-related heartburn. However, recent research has found that Zantac® contains dangerously high levels of NDMA, up to 3,000x more than the safe limit.
Prior to the FDA announcement, over a million Zantac® prescriptions were being issued each and every year. Now, thousands of patients are taking Zantac's® parent company, Sanofi®, to court in order to seek justice for themselves and their loved ones.
Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Zantac®, Sanofi®, or any government agency.
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