Consumers Who Have Used Zantac® And Are Now Suffering From Certain Cancers Are Urged To Request a Free Case Evaluation For Justice and Substantial Compensation

Consumers Who Have Used Zantac® And Are Now Suffering From Certain Cancers Are Urged To Request a Free Case Evaluation For Justice and Substantial Compensation

Some of the bladder cancer symptoms that consumers of Zantac® (aka ranitidine®) consumers should be wary of may include:

  • Blood or blood clots in the urine;
  • Pain or burning sensation during urination;
  • Frequent urination;
  • Feeling the need to urinate many times throughout the night;
  • Feeling the need to urinate, but not being able to pass urine; and,
  • Lower back pain on one side of the body.

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What Zantac® (aka ranitidine®) Consumers Must Know About Its Link to Bladder Cancer?

Due to detected levels of a probable human carcinogen in ranitidine® medications, taking Zantac® may increase the risk of developing bladder cancer.

Zantac® (aka ranitidine®) lawyers stipulate that people must satisfy several conditions to potentially qualify for a lawsuit–these include proven Zantac® (aka ranitidine®) use plus a bladder cancer diagnosis and a connection between the bladder cancer diagnosis and Zantac® (aka ranitidine®) .
Only a Shield Legal Network lawyer can properly evaluate a claim, and they can help gather medical records and evidence to build a case.

    • Brand name Zantac® (aka ranitidine®) use. Potential claimants have to prove they took the brand name Zantac® made with ranitidine®–or proof of prescription–for at least one year before being diagnosed with cancer.
    • Demonstrate a bladder cancer diagnosis. The main injury claimed in Zantac® and ranitidine® lawsuits is cancer–with potential claimants having to have a diagnosis of bladder cancer.
  • Connection Between Cancer Diagnosis and Zantac. Taking higher medication doses can help prove the connection–the length of time someone has used the drug also affects the case.

Those with bladder cancer and a history of taking Zantac® can file a legal claim against ranitidine® manufacturers.

Billions in profits made on unsafe Medication

How does Zantac® (aka ranitidine®) cause bladder cancer?

Glaxo Holdings Ltd® (aka GSK® or GlaxoSmithKline®) created and sold Zantac® beginning in 1983 to reduce excess acid produced in stomach cells.

It was first approved for short-term use only by the Federal Drug Administration (FDA) for its potential to cause cancer if prescribed in long-term use–however, Zantac® began being marketed for long-term maintenance use.

Since over-the-counter Zantac® (aka ranitidine®) contains high levels of the potentially dangerous chemical N-nitrosodimethylamine (NDMA), it has potentially been linked to several types of lifelong cancers–including bladder cancer.

  • The FDA advises the public to not ingest more than 96 nanograms of NDMA daily. 
  • Although food and water can both be contaminated with NDMA, the known levels of the chemical aren’t enough to cause actual harm.
  • One 150mg tablet of ranitidine showed more than 47,000 nanograms of NDMA in urine samples tested.

We believe that these bladder cancer victims should get the compensation and justice they deserve by addressing the makers of Zantac® (aka ranitidine®) in a court of law. 

Zantac® and Bladder Cancer in the News

2021

The FDA told all manufacturers to stop selling Zantac made with ranitidine in the United States in April 2020 because NDMA contamination can increase over time.

2021

New Study Suggests Those Taking Zantac at a Higher Risk for Bladder Cancer

2020

Because of the commonality of facts and claims, all Zantac lawsuits were consolidated into the U.S. District Court for the Southern District of Florida on February 6, 2020.

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Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with a Zantac®, Sanofi®, Zantac's® generic manufacturers, or any government agency.