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IF YOU OR A LOVED ONE SUFFERED AFTER TAKING ZANTAC®, YOU MAY BE ENTITLED TO FINANCIAL COMPENSATION!

IF YOU OR A LOVED ONE SUFFERED AFTER TAKING ZANTAC®, YOU MAY BE ENTITLED TO FINANCIAL COMPENSATION!

• STOMACH CANCER
• BREAST CANCER
• SMALL INTESTINE CANCER
• BLADDER CANCER
• KIDNEY CANCER
• PANCREATIC CANCER
• AND MUCH MORE

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Zantac Lawsuit

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How it works

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Fill Out The Form

Answer a few basic questions in our free online evaluation to see if you qualify

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review your case

Get in contact with an attorney for a free consultation to discuss your options

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file your claim

We will prepare and file your claim on your behalf at no cost to you.

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YOU OR A LOVED ONE MAY BE ELIGIBLE FOR compensation

For decades, Zantac® (ranitidine) was used to treat the symptoms of heartburn and acid reflux disease. While Sanofi®, Zantac's® manufacturer, stated that the drug was safe, recent evidence suggests that NDMA (a cancer-causing carcinogen) is released after patients take Zantac®. Independent laboratories have come forward to confirm that each 150mg Zantac® dose may produce between 2.4 million and 3.2 million nanograms of NDMA, over 3,000x more than the limit set forth by the FDA.

Now, innocent victims of Sanofi's® negligence are coming forward to seek compensation against the pharmaceutical giant. Finding out if you are eligible to file a claim against Zantac's® manufacturer is 100% free.

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zantac® and cancer

as thousands of Americans suffer from cancer development, many are questioning whether their use of zantac® is to blame, especially those suffering from breast cancer and non-Hodgkin's lymphoma.

it is widely speculated that zantac's® manufacturer, sanofi®, was aware that their drug created a cancer-causing carcinogen once it was consumed, yet failed to warn the public of this imminent danger.

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zantac® in the news

January 2020

after months of testing, the FDA requested that all retailers and pharmacies stop the sale of zantac® and generic forms of ranitidine (the active ingredient inside zantac®). 

January 2020

a team of researchers found that levels of ndma, a known carcinogen, can increase in zantac® during storage, especially if the drug is exposed to high heat. this can even occur when the drug remains inside its packaging.

november 2019

multiple generic forms of zantac® sold over-the-counter were recalled from pharmacy shelves across America as more concern grows about the link between the drug and cancer.

September 2019

the FDA releases a statement warning patients and healthcare workers that a chemical impurity in Zantac® and its generic forms may lead to cancer.

2001

the fda requires zantac® to make the first of multiple revisions to the drug's label.

1995

sanofi®, zantac's® manufacturer, wins an approval that will allow them to sell zantac® as an over-the-counter medication.

1995

zantac® becomes the world's best selling drug, with over $1 billion in sales worldwide.

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