Zantac is a popular acid reflux medication. Approved by the U.S. Food and Drug Administration (FDA), many patients in the United States have been relying on Zantac as an antacid. However, Zantac use has recently come under fire as a cancer risk. As such, the drug companies behind the product are in the midst of a class-action Zantac lawsuit.

If you or a family member take Zantac and have experienced any number of adverse side effects, here’s what you need to know about the probable human carcinogen, cancer risks it increases, and filing your own lawsuit.

Zantac Background

Zantac has been around since the 1980s. It’s available both as an OTC medication and also as a prescription. Zantac, also known as ranitidine hydrochloride, works to decrease the amount of stomach acid you can produce. It helps to prevent gastroesophageal reflux disease and some patients even take Zantac to aid with allergies as part of their treatment regimen.

For years, there have been studies linking ranitidine medicines like Zantac and some generic equivalents to various types of cancer. The pharmaceutical companies behind the medication allegedly concealed their extensive experience with this personal injury and cancer diagnosis risk from millions.

Zantac Allegations

In 2019, the FDA began investigating the links between the ranitidine product developed by Zantac’s manufacturers (Sanofi and Boehringer Ingelheim) and the cancer claims. When the FDA tested 150 Zantac pills, the organization discovered that something was off. All of the pills contained around 3,000 times more of the active ingredient NDMA (n-nitrosodimethylamine) than the FDA recommends for daily intake. Many Zantac lawsuit attorneys also disagree that there are any safe NDMA levels in the Zantac products.

As a result, many patients have been diagnosed with stomach cancer, bladder cancer, liver damage, raised blood pressure, and other serious injuries. The FDA is also looking into generic ranitidine products for possible links as well. Several patients have taken matters into their own hands and filed a Zantac cancer lawsuit as a result of their diagnoses or even wrongful death caused by both over-the-counter Zantac and prescription Zantac.

Zantac Cancer Lawsuits

The ultimate goal of the Zantac class action lawsuit is to hold the drug manufacturer accountable for hiding the connections between stomach cancer, bladder cancer, and Zantac products. If you took prescription or over-the-counter Zantac or other ranitidine medications, then you should get involved in one of these class action lawsuits or file a Zantac cancer lawsuit of your own.

Whether you’re seeking financial compensation or other damages, having the right legal team can make a world of difference. Many United States Zantac lawyers are working with plaintiffs to help with these lawsuits. Several law firms are even in communication with the FDA to learn more about the serious injuries and risks posed by Zantac products and about the flawed manufacturing process.

If you’re going to file a lawsuit, you’ll want to consult with the right attorneys. You’ll also want to have your medical records on hand to bolster your chance at success. Not only will these show your continued use of Zantac but they can also display any health issues or serious injuries you’ve incurred as a result of taking ranitidine medications. You should come prepared to discuss financial compensation stemming from your Zantac cancer lawsuit and the types of damages you’re seeking.

It’s unfortunate that anyone who has taken Zantac should have to suffer the consequences of these pharmaceutical companies’ actions. As the FDA continues to investigate these claims against Zantac, it’s critical that you consult with a law firm and discuss your case. Help is available to you and, hopefully, justice will be served.