GSK Agrees to Pay $2.2B in Zantac Lawsuit Settlement Resolving 93% of State Court Cases

Published:

October 14, 2024

  • Defective Products
gsk zantac lawsuit settlement

GSK settles to avoid further litigation, maintains no admission of wrongdoing

In a landmark settlement, pharmaceutical giant GlaxoSmithKline (GSK) has agreed to pay $2.2 billion to settle approximately 80,000 Zantac lawsuits.

 

The lawsuits allege that Zantac, a popular heartburn drug, contained a probable carcinogen called N-Nitrosodimethylamine (NDMA), putting consumers at risk for several types of cancer. 

 

The settlement is significant in the ongoing litigation surrounding Zantac and ranitidine-based products.
 

 

How the Heartburn Drug May Cause Cancer 

At the heart of the Zantac lawsuits is the connection between ranitidine, the active ingredient in Zantac, and the formation of NDMA. 

 

Research has shown that ranitidine can break down over time or when exposed to high temperatures, leading to the creation of NDMA, a substance classified as a probable human carcinogen by the World Health Organization.

 

Studies have linked NDMA exposure to an increased risk of several types of cancer, including:

  • Stomach cancer
  • Liver cancer
  • Bladder cancer
  • Pancreatic cancer
  • Esophageal cancer

 

Plaintiffs in the Zantac lawsuits allege that long-term use of the medication led to the development of these and other cancers. 

 

They argue that GSK and other manufacturers failed to test their products properly, ignored warning signs, and did not provide adequate warnings to consumers and healthcare providers.

 

Timeline of the Zantac Controversy

The Zantac lawsuits have been a major legal battleground since 2019 when the U.S. Food and Drug Administration (FDA) issued a warning about the potential presence of NDMA in ranitidine medications. 

 

Since then, Zantac litigation has been building for several years, with key events including:

  • June 2019: Online pharmacy Valisure detects NDMA in ranitidine samples and petitions the FDA to investigate.
  • September 2019: FDA confirms the presence of NDMA in some ranitidine products and launches an investigation.
  • October 2019: Several manufacturers, including GSK, voluntarily recall Zantac and generic ranitidine products.
  • April 2020: FDA requests to remove all ranitidine products from the market due to concerns about NDMA contamination.
  • June 2020: Zantac MDL (multidistrict litigation) is formed in the Southern District of Florida to consolidate federal lawsuits.
  • February 2022: First bellwether trials in the Zantac MDL are scheduled to begin.
  • October 2024: GSK announces a $2.2 billion settlement to resolve most Zantac lawsuits.

 

The settlement comes after extensive litigation, including consolidated proceedings in federal and state courts. The resolution of these cases marks a significant milestone for plaintiffs seeking compensation for their injuries.

 

Breaking Down the GSK Zantac Lawsuit Settlement

Under the settlement terms, GSK will pay up to $2.2 billion to resolve approximately 80,000 Zantac lawsuits pending in U.S. state courts.

 

Structured payout

The courts will structure the settlement to allow GSK to spread out the payments over several years, reducing the immediate financial impact on the company.

 

Federal claims excluded

The settlement resolves about 93% of the state court cases currently pending against GSK but does not cover all Zantac lawsuits. Some federal cases and claims against other manufacturers remain ongoing. GSK has also agreed to pay an additional $70 million to settle a related whistleblower lawsuit filed by a Connecticut laboratory.

 

GSK admits no wrongdoing

The manufacturer maintains that there is "no consistent or reliable evidence" that Zantac increases the risk of cancer and affirms it based its decision to settle on a desire to "avoid further litigation costs and uncertainty," allowing the company to focus on the long-term interest of the company.

 

The Future of Zantac Litigation

While the GSK settlement is a significant development, it does not mark the end of the Zantac litigation. 

 

Similar cases 

Other manufacturers, such as Pfizer, Sanofi, and Boehringer Ingelheim, also face lawsuits alleging that their ranitidine products caused cancer.

Some of these companies have already reached settlements, while others continue to defend against the claims in court.

 

Federal cases pending

In addition to the state court cases covered by the GSK settlement, thousands of federal Zantac lawsuits are still pending in the MDL. These cases are progressing through the legal system, with bellwether trials scheduled to begin in the coming months. 

Early trial outcomes will help shape the future of the litigation and may influence potential settlements by other manufacturers.

Frequently Asked Questions

The Zantac lawsuit alleges that the popular heartburn medication, which contains the active ingredient ranitidine, can break down into a probable carcinogen called NDMA. Plaintiffs claim that Zantac manufacturers, including GSK, failed to warn consumers about the potential cancer risk associated with the drug.

GSK has agreed to pay $2.2 billion to settle approximately 80,000 Zantac lawsuits pending in U.S. state courts. The settlement resolves about 93% of the state court cases against GSK.

Specific eligibility criteria are still being determined, but generally, claimants will need to provide evidence of Zantac use, a cancer diagnosis potentially linked to NDMA exposure, and a timeline connecting their drug use to their diagnosis. An experienced attorney can help determine if you qualify.

Studies have linked NDMA exposure to an increased risk of several cancers, including stomach, liver, bladder, pancreatic, and esophageal cancer. If you developed one of these cancers after taking Zantac, you might have a valid legal claim.

Add Comment