Zantac is a heartburn drug that has recently been pulled from the market in 2022 due to mounting lawsuits claiming the drug causes cancer. 1 Zantac, chemically known as ranitidine, first raised concern in 2018. 1
In 2020, Zantac was pulled from the market due to is linked to unacceptable levels of N-nitrosodimethylamine (NDMA), a probable carcinogen. 2 & 4
Zantac and genetic ranitidine were used by millions of Americans prior to the recall. 4
More than 2,000 lawsuits have been filed in federal courts in Florida alone and the first federal court trials are scheduled for some time next year, in 2023. 1 & 2
If you or a loved one have suffered injuries such as cancer, and even death, please take the time to read this article and determine if you are a candidate for the ongoing Zantac lawsuits.
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Injuries and Side EffectsSettlementsPast LawsuitsCurrent LawsuitsEligibilityScientific StudiesFrequently Asked QuestionsLawsuits claim that there is an impurity called N-nitrosodimethylamine (NDMA), a probable carcinogen, that has directly resulted in the plaintiffs' cancer diagnosis.1
GSK and Sanofi, former drug manufacturers of ranitidine, claim there is no scientific evidence to indicate that Zantac, or its generic version of ranitidine, causes cancer. 2
Zantac makers however claim that the NDMA levels found in the medicine are close to the common found in grilled, smoked, packaged, and frozen meats and fish. 1 & 2
Yet studies have shown that Zantac and the generic medicine Remitine breaks down into NDMA, a known carcinogenic. 5
Recent studies have even found that certain diets and the storage conditions of ranitidine in high temperatures can cause the pill to become even more dangerous with extremely dangerous levels of NDMA. 5
Although the first Zantac case has to be voluntarily dismissed from courts, generic drugmakers agreed to pay a combined settlement of $500,000 to Bayer, the plaintiff alleging the medication caused his esophageal cancer. 2 & 4
The plaintiffs' attorneys maintain "Ultimately, the overwhelming body of science supports the fact that (Zantac) degrades into NDMA, a chemical recognized by the FDA as a Class 1 genotoxic carcinogen, and causes cancer." 2
Studies have shown that Zantac and the generic medicine Remitine breaks down into NDMA, a known carcinogenic
The first Zantac lawsuit over cancer that was to go before a jury was dismissed after a settlement agreement was reached with the plaintiff and generic drug makers. 4
Have you or a loved one been diagnosed with Bladder cancer/Esophageal cancer/Gastric cancer/Liver cancer/Pancreatic cancer after using Zantac?
Take the time to see if you qualify.
As of August 2022, trials are expected to begin in California and federal court in early 2023. 4
Generic drugmakers agreed to pay a combined settlement of $500,000 for the first Zantac case to be settled out of court
Millions of America have taken Zantac and the generic version ranitidine for heartburn and acid reflux treatment.
Zantac injury lawsuits claim manufacturers of the drug knew of the NDMA contamination in their products and that these products resulted in their various cancer diagnoses. 4 & 5
Currently, all litigation is in the initial stages and trials should be going to court within the upcoming year. 9
If you are a loved one who was diagnosed with mesothelioma or ovarian cancer due to the usage of J&J talc powder, please have your case reviewed by a legal professional.
Have you or a loved one been diagnosed with Bladder cancer/Esophageal cancer/Gastric cancer/Liver cancer/Pancreatic cancer after using Zantac?
Take the time to see if you qualify.
The FDA found that safe daily NDMA exposure is 96 nanograms (ng), yet independent pharmacies have found more than 3 million ng in each Zantac pill. 4
Studies have shown that Zantac and the generic medicine Remitine breaks down into NDMA, a known carcinogenic
Have you developed cancer within 20 years of the last time taking Zantac?
Medical records and proof of a Zantac prescription will need to be provided for the lawsuit.
Have you been diagnosed with cancer at age 89 or younger?
Many potential clients have been diagnosed with cancer at the age of 89 or younger.
Have you taken Zantac at least once a week for one year before being diagnosed with cancer?
Evidence to confirm the timeframe of Zantac usage and later cancer diagnosis is needed. Past lawsuits have seen individuals seeking compensation after a cancer diagnosis following the use of Zantac for at least one year. 9
Do you have evidence such as a Zantac prescription? (i.e. medical records or receipts for over-the-counter purchases)
Proof of a Zantac prescription will need to be provided for the lawsuit.
How Does Zantac Contribute to Cancer?
Who is Eligible to File a Lawsuit?
What is the Status of Zantac Lawsuits?
Has There Been a Zantac Settlement?
Case reviews are provided for free unless you are awarded compensation for your Zantac Lawsuit.
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Injuries and Side EffectsSettlementsPast LawsuitsCurrent LawsuitsEligibilityScientific StudiesFrequently Asked QuestionsImplicated Products
Zantac manufactured by Sanofi, GSK, Bayer AG, Boehringer Ingelheim GmbH, Dr. Reddy’s Laboratories Ltd, and Dr. Reddy’s Laboratotes, Inc.
Carcinogen
N-nitrosodimethylamine (NDMA)
Related Injuries
Bladder cancer; Esophageal cancer; Gastric cancer; Liver cancer; Pancreatic cancer
Top Settlement/Jury Verdict
$500,000 (settlement out of court)
Defendants
Pfizer and GlaxoSmithKline; Sanofi US Services Inc.; Sanofi-Aventis U.S. LLC; Chattem; Inc.; Boehringer Ingelheim