Zantac (Ranitidine) Cancer Settlement
vs. Sanofi, GSK, Boehringer Ingelheim, Pfizer
Manufacturers of Zantac heartburn medication face claims that the drug contained NDMA, a probable human carcinogen, and failed to warn consumers about cancer risks.
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Individuals who regularly took Zantac (ranitidine) and were later diagnosed with cancer, particularly bladder, stomach, liver, esophageal, or pancreatic cancer.
- Must have used Zantac/ranitidine regularly (at least once per week for a year or more)
- Must have been diagnosed with a qualifying cancer after using the product
- Qualifying cancers include: bladder, stomach, liver, esophageal, pancreatic, colorectal
- No age restriction on claims
Proof Requirements
Required documentation:
- Medical records confirming cancer diagnosis
- Evidence of Zantac/ranitidine use (pharmacy records, declarations)
- Treatment records
Settlement Details
Zantac (ranitidine), one of the world's best-selling heartburn medications, was pulled from the market in 2020 after testing revealed it contained unacceptable levels of N-Nitrosodimethylamine (NDMA), a probable carcinogen. Users who developed certain cancers after taking Zantac may be eligible for compensation.
Individual settlement negotiations are ongoing with payouts expected to vary significantly based on cancer type, duration of use, and other factors.
Case Information
| Case Number | 9:20-md-02924-RLR |
| Court | U.S. District Court, Southern District of Florida |
| Settlement Administrator | MDL Settlement Administrator |
| Status | open |
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