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

Consumers encouraged to seek out legal case evaluations for conditions such as…

  • Bladder Cancer
  • Esophageal Cancer
  • Liver Cancer
  • Pancreatic Cancer
  • Stomach-Gastric Cancer

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Here are the alleged dangers of Zantac® (aka ranitidine®) that may cause cancers

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 linked to several types of lifelong cancers, including:

  • Bladder cancer. A disease in which malignant (cancer) cells show signs and symptoms  such as blood in the urine and pain during urination.
  • Esophageal cancer. A cancer that can cause difficulty swallowing, chest pain, and heartburn–tricking victims into taking more to reduce the symptoms.
  • Liver cancer. Patients diagnosed with liver cancer after taking Zantac® (aka ranitidine®) typically complain of abdominal pain and swelling, plus general loss of energy.
  • Pancreatic cancer. A particularly deadly form of cancer–with common symptoms that include itchy skin, yellowing of the eyes, and abdominal pain
  • Stomach cancer. Also known as gastric cancer, this type of cancer forms over the course of many years–with a five-year survival rate for diagnosed individuals being 70%.

Not only that, but Zantac® should also not be taken with certain foods (or with any foods at all based on some studies) due to its potential to create carcinogenic chemicals in the body.

Zantac® and Vitamin C:

  • Some studies showed that adding Vitamin C to the Zantac® formula might reduce its carcinogenic effects
  • Glaxo Holdings Ltd® not only failed to add Vitamin C, they failed to warn consumers of the carcinogenic potential of the drug

Wired reveals that a 2020 study showed the Food and Drug Administration announced voluntary recalls of prescription forms of ranitidine® by two generic drug companies–Appco Pharma® and Northwind Pharmaceuticals®–bringing the total number of ranitidine® recalls to 14 in the past five months.

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

Billions in profits made on unsafe Medication

Zantac® Facts in the News

2021

Very Well Health reveals that since 1983, the FDA Adverse Event Reporting System (FAERS) has received a total of 73,240 cases with a negative effect of Zantac®.

This includes:

  • 55,891 serious cases
  • 4,926 deaths
  • 66% of cases were linked to cancer

2018

18,739,686 people in the United States were prescribed Zantac®–1,094 cases involving Zantac® were reported to the FDA in the same year.

2016

According to USA Today, a Stanford University research study indicated that urine samples of 10 people who took a 150-milligram tablet of Zantac® and found NDMA (a known carcinogen) levels far greater than the FDA's daily limits.

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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.