Injured patients can seek compensation.

Injured patients can seek compensation.

Injured by the heartburn medication Zantac?

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Zantac Lawsuit Claims

UPDATE: FDA Requests Removal of All Ranitidine Products (Zantac) from the Market 

The U.S. Food and Drug Administration (FDA) announced on April 1, 2020, it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine (NDMA) in ranitidine medications (commonly known by the brand name Zantac).

Filing a Zantac lawsuit

A Zantac cancer lawsuit may help victims recover damages for:

• Medical costs

• Lost wages

• Pain and suffering 

• Disability or permanent injury

• Punitive damages

• Wrongful death

People who developed or were diagnosed with cancer after taking Zantac may be eligible for compensation and should seek advice from legal experts.

Zantac Dangers

Zantac was introduced in 1983, as the first member of a new class of medications, known as histamine H2-receptor antagonists (H2 blockers). It has been widely marketed as a safe treatment for heartburn, acid indigestion, sour stomach, gastroesophageal reflux disease (GERD) and other conditions. 

The active ingredient in Zantac is ranitidine which has an inherent molecular structure that may react with itself. This can produce dangerous levels of the chemical N-Nitrosodimethylamine (NDMA) when exposed to high temperatures inside the human body or during transport (such as in a hot car).

For decades, NDMA has been known to increase the risk of cancer in humans. While the drug makers knew or should have known about the link between Zantac and cancer, they failed to adequately research the risk or warn users and the medical community.

Following exposure for only a few months, experts indicate that NDMA may result in the development of cancer from Zantac.

• Bladder

• Breast

• Colorectal

• Esophageal

• Kidney/Renal

• Liver

• Lung

• Pancreatic

• Prostate

• Stomach

Filing a claim is easy

Complete the form

We will contact you within 24 hours

If you qualify, we will connect you with a law firm

Zantac Lawsuit Cancers

Have you been diagnosed with any 

of the following cancers?

Free Consultation | Available 24/7

Zantac Lawsuit Claims

UPDATE: FDA Requests Removal of All Ranitidine Products (Zantac) from the Market 

The U.S. Food and Drug Administration (FDA) announced on April 1, 2020, it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine (NDMA) in ranitidine medications (commonly known by the brand name Zantac). 

Zantac Dangers

Zantac was introduced in 1983, as the first member of a new class of medications, known as histamine H2-receptor antagonists (H2 blockers). It has been widely marketed as a safe treatment for heartburn, acid indigestion, sour stomach, gastroesophageal reflux disease (GERD) and other conditions. 

The active ingredient in Zantac is ranitidine which has an inherent molecular structure that may react with itself. This can produce dangerous levels of the chemical N-Nitrosodimethylamine (NDMA) when exposed to high temperatures inside the human body or during transport (such as in a hot car).

For decades, NDMA has been known to increase the risk of cancer in humans. While the drug makers knew or should have known about the link between Zantac and cancer, they failed to adequately research the risk or warn users and the medical community.

Following exposure for only a few months, experts indicate that NDMA may result in the development of cancer from Zantac.

Filing a claim is easy

Complete the form

We will contact you within 24 hours

If you qualify, we will connect you with a law firm

Injured patients can seek compensation.

Free claim review