Zantac Recall Over Potential Cancer Connection - Stewart Law Offices
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FDA Pulls Zantac Off Shelves for Possible Cancer Link

The U.S. Food and Drug Administration (FDA) has ordered for the popular heartburn medication ranitidine (brand name Zantac) to be taken off the market immediately. The decision was made due to the discovery that ranitidine drugs may contain dangerous levels of N-Nitrosodimethlyamine (NDMA), a probable human carcinogen.

The recall affects both prescription and over-the-counter (OTC) ranitidine medications. Hundreds of Zantac lawsuits are already pending throughout the United States, alleging that the drugmakers failed to warn the public of the dangers of NDMA and that their inaction led to diagnoses of cancer in some consumers.

If you or a family member took Zantac or a generic ranitidine product, you may have a case for compensation. The experienced personal injury attorneys at Stewart Law Offices can evaluate your case in a free consultation.

With five locations in South Carolina and North Carolina, our lawyers can meet with you wherever you are most comfortable.

Call or contact us today to schedule a free consultation.

What Makes Zantac Dangerous?

According to a press release, the FDA’s decision was based on testing that showed NDMA levels in some ranitidine medications increased to unacceptable levels over time, particularly when stored at higher than room temperatures. However, increases in NDMA levels were also observed when the drugs were stored at normal temperatures as well.

NDMA has been linked to primary cancers of the:

  • Stomach
  • Bladder
  • Small intestine
  • Colon/rectum
  • Esophagus
  • Liver

On a lesser level, NDMA has possible associations with:

  • Early-onset prostate cancer
  • Pancreatic cancer
  • Non-Hodgkin’s lymphoma
  • Multiple myeloma

No one should have to live with a life-threatening disease caused by someone else’s negligence — particularly a pharmaceutical company’s, whose main job is to make drugs to improve public health.

Can I Sue for Damages?

Zantac lawsuits are already underway. To determine if you have a case, you will need to meet with a knowledgeable attorney with experience handling defective drug claims.

Several steps must be taken to decide if you may be entitled to compensation:

  • Did you take Zantac or ranitidine? This can be established through medical records,
    prescription receipts, or statements from a doctor, even if you only took the OTC
    version of the drug.
  • How long did you take the drug? If you only took the medication for a short period, it
    will be more difficult to prove a connection between Zantac use and your cancer
    diagnosis.
  • Do you have cancer? Proof of diagnosis can be confirmed through medical records.
  • Did Zantac cause your cancer? Here is the trickiest part of your case. Your attorney will
    need to provide compelling evidence to show that your Zantac use and cancer diagnosis
    are closely connected. For example, if you took Zantac for three years for acid reflux,
    you will likely have a stronger case than someone who used it for six months. There is
    also a latency period (the time between exposure to a cancer-causing substance and the
    development of the disease) to consider. If you took Zantac for six months and were
    diagnosed with cancer a month later, it will be more difficult to convince a judge or jury
    that ranitidine caused the disease.

Compensation in dangerous drug cases can help cover medical costs, lost income, lost earning potential, pain and suffering, and other losses stemming from the diagnosis. This money can be vitally important to keep families afloat during a cancer battle.

Diagnosed with Cancer After Taking Zantac? Learn Your Legal Rights Now

For more information about Zantac lawsuits, call or contact Stewart Law Offices today. Our North Carolina and South Carolina injury lawyers are standing by to help.