What Cancers Qualify for the Zantac Lawsuit? - Zantac, known as a heartburn medicine, has an ingredient that is carcinogenic and associated with a range of cancers. Suppose you have developed cancer after taking Zantac. In that case, it is essential to talk with a lawyer for injuries to determine what types of cancers can be included in this Zantac lawsuit.
What Is Zantac?
Zantac is a well-known heartburn medicine that is typically used to treat the symptoms of stomach acid and ulcers. Pfizer, a well-known pharmaceutical manufacturer, launched Zantac in 1981. In 2002 it was announced that the Federal Drug Administration (FDA) approved the generic version of ranitidine, which was advertised under the name Zantac. From 2002 on, it’s been estimated that millions have used Zantac as prescription or over-the-counter (OTC) varieties. The prescription strength is usually prescribed to prevent and treat ulcers in the stomach, intestines, and stomach; however, OTC products that are lower in doses are typically utilized to treat heartburn, constipation, and GERD, which is a widespread digestive disorder that affects the gastrointestinal tract.
Zantac Contains NDMA
What is NDMA? The N-nitroso dimethylamine (NDMA) is a likely human carcinogen, confirming the link between Zantac and cancer. NDMA has been associated with numerous gastrointestinal cancers like bladder, stomach, and cancers of the esophagus, pancreas, liver, and colon. NDMA is considered particularly harmful for consumption by humans because it is broken down in normal digestion into tiny particles quickly taken up by organs in internal. NDMA is also believed to break down more quickly when kept in excessively hot or humid environments over extended periods in storage facilities, on shelves in stores, or in medicine for consumers’ cabinets.
In 2019, FDA tests revealed alarming levels of NDMA found in Zantac and other ranitidine-based products. While FDA tests showed low levels of NDMA found in certain Zantac products, higher levels were detected in the ranitidine product (the generic versions in Zantac). The concentrations of cancer-causing chemicals in certain ranitidine products were determined to be 3,000 times higher than levels considered secure by the FDA. Tests also revealed that ranitidine products with older manufactured dates had more levels of NDMA and confirmed the FDA’s concerns over NDMA breaking down more quickly in the long-term storage of these drugs.
In the year 2016 in 2016, the FDA issued a series of warnings to the public regarding the possible risks posed by exposure to NDMA. In 2017 the FDA announced that it would require all makers of prescription medicines that contain NDMA to provide warning labels about the possible health hazards associated with long-term usage. On the 1st of April 2020, the FDA made public their findings regarding unacceptable levels of NDMA in ranitidine-based products and urged the pharmaceutical industry to recall the products. Since then, over 12 major pharmaceutical companies have been forced to have Zantac recalls removed from shelves in major retailers and pharmacies nationwide.
Zantac Side Effects
In the past decade, there has been a plethora of cases reported by doctors as well as consumers, and injury lawyers about serious side effects that are associated with Zantac. Commonly, serious Zantac adverse consequences reported include the following:
- Intestinal bleeding
- Breast cancer
- Prostate cancer
- Stomach cancer
- Kidney failure
- Thyroid problems
The most severe Zantac adverse reactions could be categorized under which cancers are eligible for the Zantac lawsuit. For those who suffer from severe signs and symptoms resulting from taking Zantac and have a severe reaction, it is essential to consult a lawyer for injuries who can answer any questions regarding the Zantac injury lawsuit. You can also receive compensation for cancer-related ailments or injuries.
Zantac’s less serious side effects could include nausea, constipation, vomiting, diarrhea, nausea, loss of appetite, stomach pain, headache, and insomnia. In the long run, side effects could include anemia, poor liver function, vertigo or dizziness, and meningitis.
In addition, a few people who took Zantac experienced a severe allergic reaction called angioedema. This type of reaction can cause extreme swelling of the lips, face, and throat, as well as tongue and airways, resulting in the sensation of wheezing, pain, difficulties swallowing, and breathing issues.
Determining Who Qualifies for the Zantac Lawsuit
After the FDA issued recalls of Zantac and ranitidine-based products in 2020, many Zantac lawsuits have been filed. The FDA has determined that Zantac causes cancer, but not all cancer patients are eligible to be able to file the Zantac suit for injuries. Specific criteria determine which cancers are eligible for a Zantac lawsuit.
The majority of plaintiffs who file Zantac lawsuits are people who contracted cancer following the use of ranitidine-based products. There are a lot of plaintiffs, and the number is growing. There are various class-action lawsuits, including those who took ranitidine but haven’t been sick or had any significant adverse negative effects. Plaintiffs who are suing aim to get reimbursement for the price of their prescriptions as well as an equitable remedy, such as medical monitoring.
Filing a Zantac Lawsuit
To file a Zantac-related suit for cancer, you must comply with guidelines on what cancers qualify to be included in the Zantac lawsuit. The following conditions must be met.
- It would help if you got an official cancer diagnosis from a licensed doctor.
- You need to prove that you are taking Zantac (prescription or other records from your physician or pharmacist)
- You must demonstrate a direct link between cancer diagnosis and using Zantac.
- It would be best if you had been taking Zantac for an extended period (usually at least one year and more)
Many lawsuits filed to remedy product-related injuries, illnesses, and even deaths are brought against drug makers or pharmaceutical corporations. It’s not easy to give an average settlement amount in these cases; however, If you look at the results of a Zantac lawsuit with similar lawsuits in mass tort cases involving cancer, the settlement amount could likely be up to $500,000. In cases of wrongful deaths, and instances that involve untested or potentially dangerous drugs and drugs, the settlement could be more. This is particularly relevant for cases in which it is discovered that the FDA has linked these medications to carcinogenic substances and has issued a recall of the drugs.
If a Zantac lawsuit is made, patients who have cancer have to file the suit within the Zantac time limit. In Illinois, the statute of limitations is two years from when the incident occurred. If you get cancer following taking Zantac, it is essential to have a medical diagnosis and proof of a direct relationship to Zantac are crucial for obtaining the success of your lawsuit.
You can contact The Justice Now Lawsuit Experts to get personal Case Evaluation for Free. So, If you think you have major health issues such as Parkinson’s disease or cancer. Feel free to contact us and we are glad to analyse your case and help you get the proper compensation you deserve.
