Is Zantac bad for your liver health?
Even though drugs have different effects on different individuals, research reveals that Zantac can be extremely harmful to the liver for the majority of individuals. This can lead to acute liver injury, liver toxicity, and even liver cancer.
Ranitidine, also known as Zantac, is an over-the-counter medication that was originally launched in the United States in 1983. Zantac was a regularly recommended medication for patients with heartburn, acid indigestion, and gastrointestinal reflux. esophageal (GERD or acid reflux).
The drug Zantac was recently found to produce toxic amounts of NDMA, a chemical associated with cancers and liver disease. For this reason, people who have suffered liver damage after taking Zantac can sue the manufacturers of the drug for compensation.
Rosenfeld’s personal injury attorneys represent injured people who may be qualified to file a claim against the makers of Zantac after being injured by a reputable over-the-counter or prescription drug.
What is the procedure of the Zantac trial?
The process begins when the plaintiff or victim files a lawsuit against the trademark in court (defendant). The respondent will then respond to your complaint by filing a response. The plaintiff and defendant will review the medical records and other data listed in the case, along with the defendant’s response, during the discovery phase. You will be asked to show certain documents during this step, and you will be questioned. The process ends with pre-trial motions to determine whether evidence can be presented in court, followed by the trial. The method is the same as for any other legal action, but the time required to complete each step varies.
For a free lawsuit consultation, contact our law firm
When you or a loved one has been diagnosed with liver cancer after taking Zantac, you may be eligible for financial compensation from the drug manufacturer through a lawsuit against Zantac.
As a result of the Zantac cases, we have received an increasing number of queries and requests for assistance. We will also be happy to help you obtain compensation for your problems.
What is NDMA?
Zantac was found to contain N-nitrosodimethylamine, a proven B2 carcinogen (a carcinogen called NDMA) as discovered by research. For ages, the Environmental Protection Agency (EPA) and the Agency for Toxic Substances and Disease Registry have designated NDMA as a carcinogenic toxin. It does not dissolve in the human body or even in the environment, as concluded after performing several important types of research. According to the World Health Organization, exposure to this carcinogen accumulates over time, leading to liver damage and other adverse health effects.
In the United States, Zantac is currently not available for purchase. Initially, producers of ranitidine-containing pharmaceuticals like Appco Pharma LLC, Northwind Pharmaceutical, and Sanofi Pharmaceutical voluntarily recalled their products. The Federal Drug Administration (FDA) legally banned Zantac and any other drugs containing ranitidine in April 2020, citing mounting evidence of NDMA toxicity and the link between NDMA and Zantac.
Is it possible that Zantac causes liver disease or cancer?
Zantac (ranitidine) was among the most commonly prescribed medications in the United States, with approximately 15 million prescriptions written each year to treat gastric disorders.
The United States Food and Drug Administration issued an advisory in September 2019 warning of the dangerous levels of NDMA present in Zantac. Constant exposure to this substance has been linked to many health problems, including liver disease, kidney failure, and cancer.
Around this time there is no way to know how likely you are to have liver damage after taking Zantac. There is, however, some evidence that the NDMA present in Zantac may increase the risk of developing liver problems.
The liver is one of the most vital organs responsible for processing toxins in the body. There is evidence that when NDMA comes into contact with the liver, it stimulates the release of inflammatory cytokines, which in turn cause liver inflammation and scarring. Exposure of the liver to high levels of NDMA also causes serious liver disease such as enlarged/swollen liver, reduced liver function, and liver cancer.
Liver disease caused by Zantac can further lead to health problems such as jaundice, bloody vomiting, kidney failure, swelling of limbs and stomach, uncontrollable itchy skin, weight loss, confusion mental and liver failure.
Treatment for liver disease can be very expensive and if the disease gets worse, it can also lead to complete disruption of normal life, job loss and other consequential health issues.
If you or a loved one took Zantac regularly for a medical condition and had major liver problems, you may be eligible to join a class action lawsuit against the Zantac drug makers.