Tulsa Zantac Lawyers
Warriors and Friends in Your Fight Against Negligent Drug Manufacturers
In September of 2019, an independent online pharmacy discovered a disturbing truth about Zantac. According to the Valisure Citizen Petition on Ranitidine, Zantac and its generic versions (ranitidine) contain “extremely high levels of N-Nitrososdimethylamine (NDMA).”
For context, NDMA is a probable human carcinogen, which means it is a substance that can cause cancer in human beings. Exposure to NDMA through Zantac and other ranitidine products has already led consumers to develop a variety of digestive tract cancers.
Zantac is a brand-named drug produced by Sanofi. It relies on the active ingredient, ranitidine, to relieve and prevent heartburn. Ranitidine is an H2 (histamine-2) blocker and prescription-level doses can also treat and prevent ulcers in the stomach and intestines.
Introduced in 1986, Zantac quickly garnered popularity and became one of the best-selling drugs in history. By 1988, it had become the first medication to surpass $1 billion in annual sales. Consumers and prescribers alike chose Zantac because they assumed it was safe.
Unfortunately, recent guidance from the U.S. Food and Drug Administration (FDA) proves this is not the case. On April 1, 2020, the FDA asked Sanofi and all ranitidine manufacturers to withdraw their products from the market immediately and encouraged consumers to stop taking pills, tablets, and liquids.
If you have Zantac or other ranitidine medications at home, follow FDA instructions to safely dispose of them and do not buy more.
To discuss any concerns you have with an attorney, please call us at (918) 347-6456.
What Is NDMA?
N-Nitrosodimethylamine or NDMA is an environmental contaminant found in our water, grilled meats, dairy, vegetables, and other food products. In small doses, it is relatively harmless, but daily exposure exceeding 0.096 micrograms or 0.32 parts per million (ppm) can lead to an increased risk of cancer.
FDA testing revealed that some ranitidine products contained up to 0.86 micrograms of NDMA per tablet or oral dose and up to 2.85 ppm.
One or two doses every once in a while is unlikely to cause harm, but if you have taken Zantac regularly for 1 year or more or weekly for at least 6 months, please contact our Tulsa Zantac attorneys ASAP.
Filing a Lawsuit
Zantac cancer lawsuits are already underway in Oklahoma and other states. On January 3, 2020, a New Jersey woman filed a complaint alleging once a day Zantac use led to her esophageal cancer. In Florida, another woman sued drugmakers Sanofi, Pfizer, Boehringer Ingelheim, and GlaxoSmithKline because their ranitidine products allegedly caused her colon cancer.
Lawsuits are popping up all over the United States for related ailments, such as:
- Rectal cancer
- Stomach cancer
- Bladder cancer
- Liver cancer
- Kidney cancer
- And other diseases
Due to the growing number of suits filed in federal court, the U.S. Judicial Panel on Multidistrict Litigation is considering a class action to consolidate claims.
If you are interested in joining a class-action lawsuit in Oklahoma, our firm can help.
Why Choose Richardson Richardson Boudreaux, PLLC?
At our firm, we do whatever it takes to achieve the best results for our clients. To date, we have obtained more than $500 million on our clients’ behalf, and our past success defines our continued success.
Further, our attorneys have been seeking justice for the injured and bereaved since 1984. We have plenty of experience handling dangerous drug cases and toxic torts. Our legal team understands the gravity of a cancer diagnosis and wants to help ensure you receive the appropriate compensation.
For the warriors and friends you need for your legal battle, please contact the Richardson Richardson Boudreaux, PLLC team at (918) 347-6456 today. You can also request a free consultation online.
We look forward to putting our skills and extensive resources to work for you!