Due to the rigorous testing and production protocols governing pharmaceutical drugs in the United States, people expect their medications to be safe. Unfortunately, the process does not always ensure consumer safety. Sometimes the discovery of a significant danger comes years after a drug’s release.
This was the case with the popular heartburn medication, Zantac. Recently, authorities discovered that it contains a carcinogen dangerous to a consumer’s health. If you or a family member have taken this heartburn medication, consult a Western Pennsylvania Zantac lawyer to discuss your potential personal injury case. A knowledgeable mass torts attorney could empathize with the health complications you face and fight to hold the drug manufacturer accountable for the harm it caused.
How is Zantac Dangerous?
The heartburn drug, first released in 1983, has been used by millions of Americans in both its over-the-counter strength and prescription formats. In September 2019, the United States Food and Drug Administration (FDA), announced the detection of a compound called N-nitrosodimethylamine (NDMA) in Zantac and other drugs containing the ingredients ranitidine or nizatidine.
NDMA can cause adverse effects on the internal organs. For instance, liver issues such as inflammation, scarring, or fibrosis can occur. Additionally, prolonged exposure may result in a decrease in organ function and an increase in the likelihood of tumor development. Symptoms of overexposure to NDMA may include:
- Stomach cramps or pain
The FDA detected NDMA above the acceptable daily intake levels and launched a campaign to inform the public of this dangerous component. Since the announcement, the FDA is investigating, conducting further testing, and asking drug manufacturers to do the same.
The agency has advised patients in Indiana taking prescription heartburn drugs containing ranitidine or nizatidine to speak with their doctor about other treatment options. It advises those using over-the-counter medications with either ingredient should switch to a non-ranitidine or nizatidine medications. A Western PA lawyer could analyze a Zantac consumer’s symptoms and determine their eligibility for a civil claim.
Since drug manufacturers must detect and disclose the harmful side effects of a medication, when they fail to do so, they can be liable for the resulting losses to consumers. A Western Pennsylvania attorney could facilitate the filing of a Zantac claim and fight for a claimant’s best interests in seeking financial recovery.
Damages are compensation for losses a person has suffered as a result of a drug manufacturers’ wrongdoing. Some of the potential awards an injured person may receive include:
- Past medical expenses incurred as a result of taking the drug
- Expected future medical expenses
- Lost income from time taken off of work due to drug-related injuries
- Expected lost earning capacity
- A variety of physical pain and mental suffering-related damages stemming from injuries, diagnoses, treatment, and life alteration
- Punitive damages, if warranted
Contact an Indiana Zantac Attorney Today
Consumers may have a claim if they took Zantac and now are experiencing severe losses as a result. Although a legal settlement or award cannot take away the harm done by the drug, it can alleviate some of the stress of dealing with the resulting complications.
A Western PA Zantac lawyer could help you build a strong case to hold the negligent pharmaceutical company responsible for your losses. Reach out to a Marcus & Mack lawyer today to schedule a free initial case consultation.