Many people Zantac took to treat heartburn, ulcers other stomach issues. Doctors prescribed the drug and customers purchased it over the counter. However, the product was later discovered to have a negative health effect that saw its manufacturers face lawsuits. If you suffered complications after taking this drug, contact our class action lawyers today to find out if you could be eligible to file a Phoenix Zantac lawsuit.
Testing of Zantac tablets showed that the product increased the risk of the user growing cancer. Its manufacturer was aware of this risk and neglected to inform the customers. Their greed, therefore, resulted in the death of many people, with tens of thousands of others developing different health problems. The law gives you the right to find justice for these wrongdoings and maintain the manufacturers of Zantac responsible.
The FDA examined more than a hundred Zantac tablets and found they contained cariogenic compounds. The levels were just two thousand times higher than the FDA recommended daily limit. The primary carcinogenic element in Zantac is called nitrosodimethylamine or NDMA.
What Is Zantac Used For?
Ranitidine is a generic version of Zantac that has been found to influence the digestive tract. It lowers the production of stomach acid. Many health professionals previously prescribed Zantac to help treat gastrointestinal complications such as peptic ulcers, Zollinger-Ellison syndrome, heartburn, intestinal ulcers, stomach ulcers, and stomach upset.
People could also get lower doses of Zantac as over-the-counter medication to treat their heartburn. But, such availability and access to this drug are another reason for the increased instances of health complications related to Zantac.
Zantac was initially sold from the U.S. in 1981, working its way up through the rankings to the 50th place on the list of most prescribed drugs in America.
Has the FDA Issued Warnings Against Zantac?
The first warning from the FDA about Zantac was issued in September 2019 after it had been found that the medication contained carcinogenic compounds called NDMA. The FDA test Zantac assessing for carcinogen levels, which have been found to be between 3,000 and 26,000 times greater than the recommended FDA limits.
Currently, the FDA has restricted the allowed carcinogenic amounts to no longer than 100 nanograms. When the FDA analyzed Zantac, they discovered that its NDMA amount proved to be a shocking 3,000,000 nanograms. The over-the-counter Zantac marketed in 150mg tablets and tablets have 300mg. Moreover, people using the medication need to take a pill before sleeping at night – for 6 to 8 weeks.
Given such ingredient counts in the Zantac, it thus was determined that users of the product had NDMA concentrations in their urine which were greater than average. The testing showed that these individuals have NDMA concentrations that are more than 400 times greater than if they hadn’t taken Zantac. A poll found out that many of the users might have chosen to use another sort of medicine if they had been alerted of the risks of cancer from the use of Zantac.
What Issues Has Research Linked Zantac To?
Researchers tested different Zantac consumers, and their findings indicated a substantial connection between the NDMA in the Zantac medicine and the risk of the users developing cancer. Boehringer Ingelheim and Sanofi, the makers of Zantac, were conscious of the carcinogenic properties within their goods but opted to misinform the people.
Millions of people used the medication to help them cope with different gastrointestinal issues such as duodenal ulcers, heartburn, gastric ulcers, acid reflux, sour stomach, and Barrett’s esophagus not knowing that using Zantac increased the risk of developing cancer.
Sanofi and Boehringer Ingelheim, the makers of Zantac, created well over a billion dollars in sales from selling their product while withholding sensitive information from the customers. Zantac was the first medicinal product to have reached such a listing in earnings.
While it had been promoted as an effective medication for treating several gastrointestinal problems, the use of the drug caused catastrophic injuries for its own consumers. Many people that used the merchandise have resisted Sanofi and Boehringer Ingelheim, seeking compensation for their suffering and pain. The cases they’ve filed against the manufacturer of Zantac cite knowingly deceiving consumers about the risk of using the product put users in harm’s way by withholding pertinent safety advice about Zantac.
What’s the Definitive Link Between Zantac And Cancer?
NDMA is known to harm various organs in the body. NDMA is one of the primary elements in Zantac. It can affect the liver, stomach, lungs, and kidneys along with other organs resulting in various medical conditions, for example:
- Kidney tumors
- Cancer of the stomach
- Lung tumors
- Liver tumors
- Liver scarring
Some data seems to suggest that the NDMA levels in Zantac aren’t high enough to cause the growth of cancer in humans. But that doesn’t imply that NDMA isn’t a carcinogen. Lengthy exposure to NDMA could result in the formation of cancerous growths.
It’s this fact which prompted many health experts to advise against the long-term usage of Zantac. The FDA says that individuals who have digestive complications and desire medications should think about different alternatives and speak with a health practitioner about the best choices available that are safer than Zantac. The market does have medications that don’t have NDMA and still offer the same health benefits as Zantac.
Is There a Recall Issued for Zantac?
Based on its investigations, the FDA requested that manufacturers take all Zantac and Ranitidine off the market in April 2020. Many retailers that had Zantac had already taken the necessary measure of protecting their customers by discontinuing the sale of the product while the FDA’s investigations were ongoing. A number of manufactures also voluntarily recalled ranitidine medicines before the FDA’s request in April.
Have There Been Lawsuits Filed Against the Manufacturers of Zantac?
Thousands of people around the United States were exposed to NDMA following using Zantac and developing health complications. These people banded together to file a number of lawsuits against the merchandise and its manufacturers. Individuals that were diagnosed with cancer after using the medication might qualify to seek reimbursement, more so when the affected areas are the liver, bladder, and stomach. The claims could be for the following damages:
- Medical expenses for issues attributed to the usage of Zantac
- Pain and discomfort
- Loss of income and ability to earn in the future
- Loss of quality of life
- Punitive damages
The class-action lawsuits are a significant help and source of hope for many who have been subjected to NDMA after using Zantac as time passes. Many of the victims get financial settlements that will cater to their different expenses, including medical expenses. The awarded amount might also consist of cash which will cover lost wages.
The class-action lawsuits have also set a precedent that compels drugs and pharmaceuticals companies to stick to strict tagging criteria. Furthermore, they have been the driving force behind new laws which are enacted so that they can shield consumers for exposure to hazardous products.
The cases filed against Zantac or its manufacturers are done the exact same way as a personal injury lawsuit. It’d be best if you learned more about the procedure involved and how they work before you file a lawsuit. The actions that you take from the onset of the process will affect the results. That is why you should consider working with an experienced Phoenix Zantac attorney who will all the legalities related to your situation and compensation case.
Develop a Winning Plan for Your Phoenix Zantac Lawsuit
In case you lost a loved one since they have been taking Zantac, then you need to think about handling the matter as a wrongful death suit. At Class Action Lawyer Coalition, we have accomplished attorneys that will help come up with a solid case and give you the best chance of being fully compensated for your pain, distress, and losses. They will be available to guide you about the steps to take so you avoid making mistakes that can dent your odds of winning the utmost compensation.
We have experienced mass tort attorneys that will take you through different aspects of your situation to help you understand what your choices are and the steps to take. We believe that you play a substantial role in the process as we put together a winning strategy. You can help our attorneys gather the evidence needed, which is essential in setting the total amount of compensation you need to get.
If you or a loved one were harmed by Zantac, you might be eligible to sue the makers of this medication for compensatory and punitive damages. Our experienced lawyers will help ascertain the amount you deserve based on your losses. The figure is attained through a careful process that will make certain you receive whatever you are owed.
When you are to use seeking skilled legal counsel and assistance for your Zantac lawsuit, our team of experienced attorneys will help develop a winning formula for your case. We will schedule a free, non-obligatory consultation to discuss your case. If we take on the case, we will be fully committed to ensuring that you recover the most damages. We will do everything possible to hold the drug manufacturers liable for your pain and discomfort. Contact us today.