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FDA Pulls Zantac Off Shelves Over Cancer Connection

The FDA found Zantac to contain high levels of the probable human carcinogen Nitrosodimethylamine (NDMA)

The makers of Zantac have been aware of the chemical for years, but failed to disclose this to consumers – instead prioritizing profit over safety

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FDA Pulls Zantac Off Shelves Over Cancer Connection

Recently the FDA found unacceptable amounts of Nitrosodimethylamine (NDMA) in Zantac. NDMA is considered a probable human carcinogen by both the World Health Organization (WHO), and the U.S. Environmental Protection Agency (EPA).

The FDA permits a daily intake of 96 nanograms of NDMA, but testing revealed each tablet contained over 3,000,000 nanograms. That’s 3,000 times greater than the FDA’s intake limit.

NDMA is a chemical that is traditionally used in rocket fuel, and is used to purposely infect lab animals with cancer for research purposes.

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As seen on:

Zantac at Fault

Zantac was released in 1983 and hit $1billion in sales by just 1986. In 1988 it was praised as the “single-largest-selling prescription drug, ever” by their CEO.  

However, studies suggest the makers of Zantac were aware of high levels of NDMA as far back as 1981, but failed to warn consumers, doctors, or government regulators of the chemical. Instead, they chose to gain profit rather than keep their consumers safe.

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If you developed cancer after using Zantac

Currently these are the forms of cancer associated with the use of Zantac:

01.

Bladder Cancer

02.

Colorectal Cancer

03.

 Ovarian Cancer

04.

Pancreatic Cancer

05.

Esophageal Cancer

06.

Stomach Cancer

07.

Intestinal Cancer

08.

Testicular Cancer

09.

Kidney Cancer

10.

Uterine Cancer

If you or a loved one have used Zantac and have cancer

contact us today to see if you’re eligible to receive significant compensation.

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