Zantac Lawsuit Attorneys-Law Offices of Kelly R. Reed

Zantac, or ranitidine in its generic form, is a popular over-the-counter (OTC) and prescription acid reducer that was used for many years by millions of people. The drug has been pulled from store shelves—first by manufacturer recalls and then by order of the US Food and Drug Administration (FDA)—because it contains a probable human carcinogen. Tragically, the makers of these drugs might have known about the cancer risks many years ago, potentially concealed evidence, and did not take action to prevent exposure.

If you or a loved one has taken ranitidine or Zantac and developed cancer, you should reach out to the Zantac lawsuit attorneys at the Law Offices of Kelly R. Reed, PLLC as soon as possible to discuss your eligibility to pursue a Zantac settlement or lawsuit to compensate you for your injuries and losses.

Our Zantac Lawsuit Attorneys Answer Your Zantac Lawsuit FAQs

Ranitidine may over time break down to create an organic chemical called N-Nitrosodimethylamine (NDMA). Studies have found that this chemical likely causes cancer and that the amount of the chemical in ranitidine increases in storage and even within the body. To help Zantac and ranitidine users understand these dangers, the Zantac lawsuit attorneys at the Law Offices of Kelly R. Reed have compiled this list of Zantac lawsuit FAQs:

What is Zantac (ranitidine) used to treat?
What level of exposure to ranitidine is dangerous?
What kind of cancer does Zantac cause?
Do I qualify to pursue a Zantac settlement?
What should I do if I developed cancer after taking Zantac?

What is Zantac Used to Treat?

Ranitidine hydrochloride, sold under the brand-name Zantac, has been used since the 1980s to treat heartburn, acid reflux, indigestion, stomach ulcers, and gastroesophageal reflux disease (GERD). The drug works by blocking histamine receptors in the stomach to reduce stomach acid.

Products that contain ranitadine include the following, among others:

Acid Control (containing ranitidine)
Acid Reducer (containing ranitidine);
Antacid (containing ranitidine);
Generic ranitidine products sold under store brand labels, including Walgreens, Walmart, CVS, Target, and Kroger;
Heartburn Relief (containing ranitidine);
Ranitidine Capsules;
Ranitadine Hydrochloride Capsules;
Ranitadine Syrup/Ranitidine Oral Solution;
Ranitadine Tablets;
Zantac 75;
Zantac 150; and
Zantac 150 Cool Mint.

What Level of Exposure to Ranitidine is Dangerous?

The FDA stated in November 2019 that it was “reasonably safe” for humans to consume 0.096 micrograms or 0.32 parts per million (PPM) of NDMA per day. However, studies have found that the amount of NDMA in ranitidine can increase during storage and within the body, so it is nearly impossible to know exactly how much NDMA exposure has occurred for each individual person when taking this product. After further evaluation, the FDA ordered that all ranitidine products be removed from the US market on April 1, 2020.

What Kind of Cancer Does Zantac Cause?

Sadly, the list of conditions potentially caused by Zantac, or ranitidine, is quite long and includes the following types of cancer:

Brain cancer;
Throat or nasal cancer;
Esophageal cancer;
Breast cancer;
Lung cancer;
Kidney (renal) cancer;
Liver cancer;
Pancreatic cancer (non-smokers);
Gastrointestinal cancer:
Stomach cancer;
Intestinal cancer;
Ovarian cancer;
Bladder cancer (non-smokers);
Prostate cancer (under the age of 65);
Testicular cancer;
Acute Lymphoblastic Leukemia; and
Non-Hodgkin Lymphoma.

If you or a loved one has been diagnosed with any of the cancers listed here after taking products containing ranitidine, you should contact the Zantac lawsuit attorneys from the Law Offices of Kelly R. Reed to discuss your eligibility to recover damages through a Zantac settlement.

Do I Qualify to Pursue a Zantac Settlement?

To qualify to file a lawsuit and pursue a Zantac settlement, you or your loved one must meet some specific criteria related to use of the product and the illness you believe resulted from that use:

The person must have used ranitidine for a minimum of one year.
The person must have used the drug at least once a week for a period of at least six months.
The use must have occurred after October 1984.
The diagnosis of injury must have been made between October 1985 and the present and within 20 years of the last dose taken.
The illness must have developed at least 12 months after first use of the drug.

Individuals over the age of 64 who have prostate cancer and those with lung cancer who have a history of smoking may not qualify. Other specific conditions may disqualify patients from pursuing a Zantac settlement through a mass tort claim, including these:

The illness developed as a result of another, non-qualifying injury or illness.
The qualifying cancer diagnosis was made prior to use of ranitidine.
The person was a resident of Michigan during use of the product.

What Should I Do If I Developed Cancer after Taking Zantac?

If you believe you or a loved one developed cancer as a result of using the drug Zantac or its generic form, ranitidine, the Zantac lawsuit attorneys at the Law Offices of Kelly R. Reed, PLLC can evaluate your specific situation, help you determine your eligibility to file a claim, and pursue a Zantac settlement or lawsuit to get compensation for your illness and losses. Reach out today to schedule a free consultation by calling (304) 292-2020 or completing our online contact form.

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Zantac Lawsuit Attorneys

Your Zantac Lawsuit Attorneys at the Law Offices of Kelly R. Reed

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