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Have you or a loved one used Zantac and as a result developed brain cancer, stomach cancer, bladder cancer, pancreatic cancer, or any other illnesses or injuries?
Those who took ranitidine-containing medications and later developed the disease filed claims in the wake of ranitidine and Zantac side effects recalls linked to cancer. N-Nitrosodimethylamine (NDMA), a potential human carcinogen, was found in ranitidine, the main ingredient in Zantac, according to FDA research.
The FDA issued a directive requiring all manufacturers to cease selling ranitidine-based Zantac in the US as of April 2020 due to the potential for NDMA contamination to increase over time. The FDA is unaware exactly how long Zantac has contained NDMA, which is a substance whose concentration rises with a drug’s shelf life. New famotidine-based drug Zantac 360 from Sanofi is not affected by the lawsuits or recalls.
Concerns about the connection between Zantac and cancer stem from a potential relationship between ranitidine and its ability to produce NDMA. Some 1980s study hypothesised a link between the drug and NDMA synthesis.
In 1983, two Italian medical researchers identified a possible link between ranitidine, the chemical name for Zantac, and the carcinogen NDMA. Dimethylamine, a component of Zantac, reacts with the letter “N” in frequently ingested foods to produce nitrosamines, nitrites, and nitrates. Zantac is always administered with food, but some early researchers advised against doing so.
According to several experts, none of the individuals who received a cancer diagnosis after using Zantac had a family history of the condition or a genetic predisposition to it. Instead, health care providers told the patients that illness was caused by their environment, which might have included NDMA exposure.
The following malignancies may result from taking Zantac:
The most common malignancy associated with Zantac is bladder cancer. If you took Zantac between January 2000 and the present and later developed one of the aforementioned cancers, be careful to see a lawyer to determine if you are qualified to file a claim.
A person must fulfil a number of prerequisites, including having used Zantac with documentation and having been given a cancer diagnosis, in order to be eligible for legal action. Since generic ranitidine is no longer covered by this policy, lawsuits can only be filed on behalf of brand-name Zantac patients.
The best person to evaluate a claim is a lawyer, who may also help build a stronger case by gathering medical documents and supporting evidence.
Other illnesses besides cancer may also be brought up in court. Make sure to inform your attorney of any new medical conditions.
You and your family might have to deal with rising medical expenditures, lost income, and poor health if you used Zantac and developed cancer. With the aid of potential settlement from a Zantac case, you might be able to cover past, present, and future medical costs.
Receive settlement for:
The anticipated average settlement or Zantac Settlement Amount in the Ranitidine Lawsuit cannot be calculated at this time. However, Sanofi-Aventis, Boehringer Ingelheim, Pfizer, and GlaxoSmithKline stock analysts and shareholders are forecasting settlement amounts from this acid reflux medication and factoring those future anticipated payouts and verdicts into the defendants’ stock prices.
Plaintiffs’ Zantac attorneys should explain this since victims want to know what the potential settlement rewards in the Zantac lawsuits would be.
This article will look at the probable settlement sums for a Zantac lawsuit in light of comparisons to earlier mass tort settlements concerning cancer.
If you think you might be able to make a Zantac cancer claim, speak with a lawyer straight soon. The filing period might be coming to an end shortly for many. The statute of limitations may be an unreasonable and tight deadline. Maintain your right to settlement by working with the top Zantac lawsuit attorney at Masstort Counsel. To contact us, dial (888) 202-1350.