Zantac Lawsuit

The FDA has warned that heartburn medication Zantac (ranitidine) may be contaminated with NDMA (N-nitrosodimethylamine), an industrial chemical, known to be carcinogenic. People who were who were diagnosed with Bladder, Kidney, Breast, Testicular, Thyroid, or Prostate Cancer after taking Zantac or store brand formulations of ranitidine may be filing Zantac (ranitidine) cancer lawsuits.

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Zantac (Ranitidine) Cancer Lawsuit

The U.S. Food and Drug Administration, along with European health agencies have warned that popular heartburn medication Zantac, and store-brand or other generic formulations of ranitidine, may contain a probable carcinogen, N-nitrosodimethylamine (NDMA).

People who developed cancer after taking prescription or over-the-counter Zantac or ranitidine may be filing lawsuits against drug manufacturer, Sanofi-Aventis or other manufacturers Lawsuits may be seeking compensation for medical costs and other damages due to cancer caused by NDMA. People of loved ones of those who were diagnosed with Bladder, Kidney, Breast, Testicular, Thyroid, or Prostate Cancer and took Zantac (ranitidine), CVS or Rite Aid Acid Controller, Walgreens’ Wal-Zan, other store brand Acid Reducer, Heartburn Relief, Acid Controller or generic forms of ranitidine for at least 60 days should seek legal advice.

Zantac / Ranitidine Recalled

Drug maker Sanofi-Aventis has recalled all its Zantac (ranitidine) medications due to concerns over potential carcinogen NDMA (N-nitrosodimethylamine), an industrial chemical which has been found in some products containing ranitidine. In addition, generic manufacturers of ranitidine medications including Apotex, GlaxoSmithKline and Sandoz and other generic manufacturers, have recalled and stopped selling their products in the U.S. and around the world.

Big box and chain pharmacies including Walgreens, Rite Aid, CVS, Target and Walmart, along with other stores have also removed all store-brand ranitidine products from their shelves until further notice. The FDA has stated that ranitidine has been permanently discontinued in the U.S. and has advised that people should discuss medication changes with their health care providers but has noted that other treatments for heartburn and GI ailments are widely available.

Zantac Cancer Lawsuit Overview

Zantac cancer lawsuit

The U.S. Food and Drug Administration has warned that heartburn medication Zantac and generic or store brand products containing ranitidine, may contain a known carcinogen, NDMA (N-nitrosodimethylamine). NDMA is an industrial chemical often found in petroleum-based products such as gasoline, diesel fuel and industrial lubricants.

Zantac’s manufacturer, Sanofi-Aventis has voluntarily recalled its Zantac medications and some drugstores and pharmacies including national chain and big-box stores like CVS, Walmart, Walgreens and others have pulled Zantac and store brand or generic ranitidine products off of their shelves over concerns about unacceptable levels of the carcinogenic compound.

People who developed cancer after taking Zantac (ranitidine) may be filing lawsuits against Zantac’s manufacturer, Sanofi-Aventis or other manufacturers.

People who may be eligible for compensation include those who took Zantac prescription or over-the-counter medication or other generics or store brands of ranitidine, regularly for at least 60 days and were diagnosed with:

  • Bladder cancer
  • Testicular cancer
  • Pediatric Testicular cancer
  • Kidney cancer
  • Prostate cancer
  • Breast cancer
  • Thyroid Cancer

If cancer diagnosis occurred more than 6 months after Zantac (ranitidine) use was stopped, it must have been taken for more than 1 year on a regular basis.

Zantac / Ranitidine FDA Warning

The U.S. Food and Drug Administration, along with European health agencies have warned that popular heartburn medication Zantac, and store-brand or other generic formulations of ranitidine, may contain a probable carcinogen, N-nitrosodimethylamine (NDMA).

According to the U.S. Environmental Protection Agency (EPA), NDMA is an environmental contaminant that is sometimes found in water and foods. Itis an organic compound used as a chemical stabilizer in gasoline, diesel fuel, rocket fuel and other petroleum-based products.

NDMA is also a byproduct of manufacturing of pesticides and other chemicals and is classified as a potential carcinogen. Zantac and other ranitidine heartburn products have been tested to contain NDMA levels that are 3,000 to 26,000 times higher than legally allowed by the FDA.

Previous NDMA Contamination of Drugs Separate from Zantac Concerns

Within the last year, NDMA contamination has been found in other medications including a number of the Angiotensin II Receptor Blockers (ARBs) group of medications used to treat high blood pressure.

Diovan and products containing ARB medication valsartan have been recalled or pulled from the U.S. market after multiple lots of the active ingredient have been shown to be contaminated with NDMA and other chemicals. All of the valsartan products appear to have been made with active pharmaceutical ingredient (API) that originated in China or India chemical manufacturing plants.

This type of contamination does not appear to be the cause of Zantac’s problems which may have originated in the drug itself which may be unstable under certain conditions. Some experts have postulated that the problem may have existed since the 1980s but is only now being recognized.

Zantac / Ranitidine Recalled

Zantac is manufactured by Sanofi-Aventis, while other formulations of ranitidine are made by generic divisions of companies such as Novartis-AG’s Sandoz unit, Apotex and GlaxoSmithKline or companies which manufacture medications for retailers such as CVS, Walmart, Walgreens and others. Sanofi has voluntarily recalled its Zantac products and other manufacturers have also issued voluntary recalls or stopped sales of generic formulations of ranitidine due to carcinogenic concerns.. Sales in the U.S., Canada, Hong Kong, Pakistan, Taiwan, India and countries in the European Union have all halted sales and the FDA has stated that product removal is permanent.

Manufacturers have been asked to examine each step of manufacturing including synthesis, formulation and storage to determine whether certain conditions may be contributing to NDMA formation. The FDA is also in the process of studying how the medication interacts with stomach-type fluids in the laboratory and has undertaken the task of conducting human studies to determine what human factors may be involved.

The FDA did not initially mandate a national recall, but has recently announced that all ranitidine products have been permanently removed from the U.S. market and will no longer be sold in the U.S. in addition to manufacturers issuing recalls, multiple stores have also pulled products from their shelves. Retailers including CVS, Walmart and Walgreens, along with others selling various generic formulations have permanently discontinued sales.

Concerns over Zantac and generic ranitidine may reach back to the 1980s but testing methods during that period may have been much less accurate and less clear. The FDA has also asked manufacturers to quickly respond with voluntary recalls if other medications appear to have the same NDMA issues, including another anti-ulcer medication nizatidine, active ingredient in Axid.

Experts have advised that patients discuss changes to their medications with a health care professional as a number of antacid alternatives are available.

Zantac Cancer – NDMA Exposure

Health experts have indicated that short term cancer risk of high NDMA levels in Zantac or ranitidine medications may be low but longer-term exposure is not well defined. In industrial use, NDMA has been clearly shown to be a potential carcinogen.

Cancers that may be related to NDMA exposure include:

  • Bladder cancer
  • Testicular
  • Kidney cancer
  • Breast cancer
  • Prostate cancer

Zantac / Ranitidine Legal Information

People or loved ones of those who have been diagnosed with cancer after taking Zantac (ranitidine) may be eligible for compensation.

People who took Zantac or other forms of ranitidine regularly for more than 60 days and were diagnosed with cancer including:

  • Bladder cancer
  • Testicular
  • Kidney cancer
  • Breast cancer
  • Prostate cancer

People who were diagnosed with one of these cancers more than 6 months after discontinuing ranitidine use but had taken prescription or brand name Zantac or certain generic or store brands of ranitidine, for more than 1 year on a regular basis.

Damages awarded in past drug injury cases have included:

  • Medical costs
  • Lost wages
  • Pain and suffering
  • Disability
  • Punitive damages
  • Wrongful death

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