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

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

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

  • Trouble swallowing
  • Chest pain
  • Weight loss
  • Hoarseness
  • Chronic cough
  • Vomiting
  • Bleeding into the esophagus

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What Zantac® (aka ranitidine®) consumers should be aware about its link to esophageal cancer?

Taking Zantac® increases the risk of developing esophageal cancer due to detected levels of a probable human carcinogen in ranitidine® medications.

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 esophageal cancer diagnosis and a connection between the esophageal 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 esophageal cancer.
    • Demonstrate an esophageal cancer diagnosis. The main injury claimed in Zantac® and ranitidine® lawsuits is esophageal cancer–with potential claimants having to have a diagnosis of esophageal 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 a history of taking Zantac® and have been diagnosed with esophageal cancer can file a legal claim against ranitidine® manufacturers.

Billions in profits made on unsafe Medication

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

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

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

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

Shield Legal Network believes that esophageal 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 Esophageal Cancer in the News

2020

According to a recently filed product liability lawsuit, the side effects of Zantac® caused a Virginia woman to develop esophageal cancer, due to carcinogenic chemicals produced by the recalled heartburn drug.

2019

Zantac users who have developed cancer are filing lawsuits against the drug’s manufacturers on several counts including Negligence, Strict Liability - Design Defect, and Strict Liability - Failure to warn.

2016

Donald Boland of Florida was diagnosed with esophageal cancer after taking Zantac three times a day since 2002.

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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.