Home » Litigation Against Zantac Manufacturers on the Rise Due to Evidence It May Cause Cancer
Attorney Sean T. Keith has been a personal injury lawyer for 30+ years, a nationally recognized Top 100 Trial Lawyer, and top car accident lawyer & motor vehicle accident lawyer in Arkansas.
This article has been written and reviewed for legal accuracy and clarity by the team of writers and attorneys at Keith Law Group and is as accurate as possible. This content should not be taken as legal advice from an attorney. If you would like to learn more about our owner and experienced injury lawyer, Sean T. Keith, you can do so here.
Keith Law Group does everything possible to make sure the information in this article is up to date and accurate. If you need specific legal advice about your case, contact us. This article should not be taken as advice from an attorney.
For the last thirty or forty years, people have come to rely on drugs like Zantac to help them treat all sorts of stomach ailments.
Most people take it to relieve heartburn and acid reflux.
Others use the drug to help with other gastrointestinal discomfort.
And, since the drug is technically an antihistamine, it is also used by people suffering from allergies.
In September of 2019, the FDA started urging pharmacies to take the drug off their shelves.
The drug is available over the counter and can also be prescribed by your physician.
According to the FDA, both versions of the drug are thought to be cancer-causing.
The Environmental Protection Agency and the World Health Organization agree.
The drug contains something called N-nitrosodimethylamine (NDMA).
The average daily intake of this chemical should be very low.
In fact, many experts argue that there are no safe levels of NDMA. The FDA has found that this drug is linked to cancer.
They have also found that this chemical becomes even more dangerous when it is exposed to high temperatures.
This means that, when the drug is stored in warm areas, it becomes very toxic.
If you have used the drug Zantac, either on a short-term or long-term basis, you may need to contact our office, as litigation against Zantac manufacturers is on the rise.
You should call and talk to a skilled injury lawyer in Arkansas right away for guidance.
Typically, when it comes to dangerous drug cases, it is the manufacturer who is named in any legal action.
For the Zantac litigation, the two major defendants are also the two largest manufacturers of the drug.
The main defendants in the class action include Sanofi and Boehringer Ingelheim.
Of course, both companies deny that their drug is unsafe.
They are also the two manufacturers who refused to voluntarily recall the drug back in September of 2019 when it was suggested by the FDA.
Of course, these are not the only companies that produce Zantac.
There are three (3) large drug manufacturing companies that also make the drug.
This includes Apotex, Sandoz, and GlaxoSmithKline.
However, all of these companies performed a voluntary recall when it was first announced that the NDMA levels in Zantac were dangerously high.
Once they chose to recall the drug from pharmacy shelves, two online pharmacies followed suit.
These companies were Vailsure and Emery Pharma.
The current litigation against Zantac manufacturers has been filed mostly against Sanofi and Boehringer Ingelheim.
They did not remove their product from the market until the FDA ordered them to do so on April 1, 2020.
It was at this point that testing revealed that the drug is unsafe, even when it has not been stored at high temperatures.
Even though Zantac has been on the market since the 1980s, it wasn’t until recently that the drug has come under attack.
The pills come in three doses: 75 mg, 150 mg and 300 mg.
The 300 mg tablet is a once per day dose.
The others are taken as needed or several times throughout the day.
The testing was done on the 150 mg tablets.
The FDA found that these tablets contained NDMA levels that were more than 3,000 times the safe daily dose.
The lawsuits against the manufacturers of Zantac allege that, not only is the drug dangerous, but that the defendants were aware of it.
They claim that Sanofi and Boehringer Ingelheim were aware that the chemicals in Zantac were dangerous and hid it.
They argue that the company intentionally hid this information so that they continue to profit from the sale of the drug.
In 2019, a suit against Sanofi and Boehringer Ingelheim resulted in the second largest verdict in the U.S. The case settled for more than $2 billion.
Another case resulted in a judgment of more than $289 million.
Today, not only are there thousands of lawsuits pending, there are now the first batch of cases being filed on behalf of children.
If you or your child have been diagnosed with cancer after taking Zantac, you need help.
You should call and talk to one of our experienced personal injury attorneys in Arkansas sooner rather than later to discuss possible litigation against Zantac manufacturers.
You only have three (3) years to file suit in Arkansas.
Call and schedule your free initial consultation as soon as possible.
And remember – you don’t pay anything until your case settles.