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Understanding the Zantac Lawsuit: Key Developments and Allegations?

As of April 2020, the U.S. Food and Drug Administration (FDA) mandated the immediate withdrawal of all Zantac brand heartburn medications, both prescription and non-prescription, due to concerns over NDMA contamination. NDMA is a substance recognized for its potential carcinogenic effects. The inaugural lawsuit against Zantac emerged in California in 2019. Within this legal action, plaintiffs level allegations against pharmaceutical companies Sanofi and Boehringer Ingelheim, claiming these entities produced, marketed, and distributed a product allegedly tainted with an industrial chemical known to be carcinogenic, despite being aware or reasonably expected to be aware of such contamination.

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Financial Compensation May Be Available Through a Zantac Lawsuit for Individuals Diagnosed with Any of the Following Types of Cancers:

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

Zantac Injuries & Side Effects

NDMA, recognized for its cancer-causing potential, also acts as a potent hepatotoxin. Exposure to NDMA in the short term can lead to liver damage, evidenced by conditions such as liver fibrosis and scarring. Long-term exposure is linked with an increased risk of developing tumors in organs, including the liver, kidneys, and lungs. The range of symptoms attributed to excessive NDMA exposure is extensive. It includes headaches, fever, and nausea, progressing to more serious conditions such as jaundice, vomiting, abdominal cramps, liver enlargement, and a decline in liver, kidney, and lung function. Dizziness is also a noted symptom.Other adverse effects that have been associated with Zantac include:

Nervous System Disorders

Arrhythmia or Tachycardia (Irregular or Rapid Heartbeat)

Vitamin B-12 Deficiency

Increased Risk of Pneumonia

Skin Rashes and Hair Loss

Low Platelet Levels in the Blood

What Is a Safe Zantac Replacement?

Deciding on a safe Zantac replacement is something you should discuss with your doctor. The FDA recommends the following Zantac alternatives:

  • Prilosec (omeprazole)

    Prilosec (omeprazole) A proton pump inhibitor (PPI) medication commonly used to treat stomach acid-related conditions, including gastroesophageal reflux disease (GERD).

  • Nexium (esomeprazole)

    Nexium (esomeprazole) A proton pump inhibitor (PPI) that reduces stomach acid production and treats GERD, ulcers, and other conditions.

  • Prevacid (lansoprazole)

    Prevacid (lansoprazole) A proton pump inhibitor (PPI) recommended for short-term ulcer and acid reflux treatment.

  • Pepcid (famotidine)

    Pepcid (famotidine) An H2 blocker that treats ulcers, GERD, and conditions that cause excess stomach acid.

  • Tagamet (cimetidine)

    Tagamet (cimetidine) An H2 blocker that reduces acid in the stomach to treat ulcers and acid reflux.

What Is Ranitidine and How Is It Used?

Ranitidine, the key active compound in Zantac, which also exists in generic forms, has been a highly sought-after medication since its introduction in the 1980s. Zantac gained popularity for its effectiveness in alleviating symptoms like upset stomach and heartburn, typically associated with acid indigestion. Available in both over-the-counter and prescription strengths, this medication catered to a wide range of needs. Prescription-strength Zantac and its generic counterparts, ranitidine, were specifically endorsed for treating gastroesophageal acid reflux disease (GERD), a condition known for causing heartburn. Additionally, these medications received approval for the prevention of ulcers in the intestines, further broadening their therapeutic scope.