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Ranitidine Recalls Triggered Cancer-Risk Litigation: What You Need to Know

Aug 13, 2024 · ~2 min read

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What Happened with Ranitidine?

Ranitidine, commonly known by the brand name Zantac, was a popular medication used to treat heartburn and acid reflux. However, in 2019, the FDA announced that some ranitidine products contained unacceptable levels of a substance called N-nitrosodimethylamine (NDMA), which is classified as a probable human carcinogen. This led to widespread recalls of Zantac and other ranitidine products across the United States.

Who’s Affected?

Individuals who took ranitidine products, especially over a long period, may be at risk for certain types of cancer. Families of those diagnosed with cancer after using Zantac may also be affected. The cancers most commonly associated with ranitidine use include:

Symptoms and Harms

While many people who took ranitidine may not experience symptoms, it’s essential to be aware of the signs that could indicate a serious health issue. Symptoms to watch for include:

If you or a loved one have experienced these symptoms after taking ranitidine, it’s important to seek medical attention promptly.

Eligible Claim Types

If you have been diagnosed with cancer after using Zantac, you may be eligible to file a claim for compensation. Potential claims include:

Practical Next Steps

If you believe you have been affected by ranitidine, here are some practical steps to take:

1. Collect Medical Records

2. Keep a Symptom Journal

3. Consult with a Healthcare Provider

4. Document Your Financial Losses

Get Help with Your Claim

If you or a loved one has been affected by the recalls of ranitidine products, it’s important to understand your rights. Pursuing.com can help you assess your situation and connect you with experienced attorneys who can guide you through the claims process.

Start your free case check today at Pursuing.com/start to see if you qualify for compensation.

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