What is Zantac?
Zantac, also known as ranitidine hydrochloride, is a class medication that helps reduce the amount of acid produced by the stomach. These drugs are formally known as H2 blockers or histamine H2-receptor antagonists. These blocker helps to treat common digestive issues like acid reflux, heartburn, duodenal ulcers, and gastric ulcers. On the market, it is available with and without a prescription. The dosage varies, but some patients can take 150mg to 300 mg per day. Zantac 360 was recently relaunched with a new name and a different ingredient (famotidine). Famotidine and ranitidine are H2 blockers that treat heartburn, acid reflux, and other stomach problems equally well.
How does it work
Zantac, as we all know, is an acid-blocking medication. This blocker helps to reduce stomach acid production. Ranitidine, the active ingredient, works by inhibiting a chemical known as histamine. The drug can begin working within just 30 minutes. It can lower the frequency and consequence of heartburn by controlling acid production for 12 hours. Having Overdoes can lead to severe effects, such as difficulty in breathing.
What are the issues with Zantac?
Every day, millions of people suffer from heartburn and stomach indigestion. For years, they relied on antacid medications to provide much-needed relief. Unfortunately, the latest evidence has shown that such medication regularly may result in increased health problems. Recent research has linked Zantac to developing several types of cancer in people who regularly use the product.
Zantac and its generic ranitidine have been linked to cancer. N-Nitrosodimethylmine was discovered in several batches of Zantac. The Environmental Protection Agency (EPA) states that NDMA is a carcinogen that has caused tumours in people exposed to it in various studies. In humans, high levels of NDMA may cause liver damage, and NDMA exposure may result in the following cancers:
- Liver cancer
- Colon cancer
- Breast cancer
- Stomach cancer
- Lung cancer
- Bladder cancer
- Ovarian cancer
- Kidney cancer
- Esophageal cancer
- Melanoma
- Brain cancer
- Thyroid cancer
- Pancreatic cancer
- Prostate cancer
Many retailers removed prescription and over-the-counter Zantac formulations from their shelves due to the NDMA content. The FDA issued an official recall in April 2020, requesting that all ranitidine manufacturers remove their products from the market for new FDA tests to be conducted. Further investigation revealed that NDMA (N-Nitrosodimethylmine) levels could rise over time if stored at temperatures above room temperature. At this point, it will become dangerous, as the number of carcinogens can reach hazardous levels, causing some individuals to develop life-threatening issues such as cancer and other health problems.
Precautions for Zantac
Ranitidine may cause severe attacks in people with a history of acute porphyria, and people with this disease should not take Zantac in conjunction with ranitidine. Researchers discovered that ranitidine could produce NDMA levels far above the FDA's allowable limits. Before taking Zantac, inform your doctor about all the medications, herbal supplements, and vitamins you use. Drinking alcohol while using the drug may increase the risk of stomach damage. Because ranitidine affects stomach acid, it can either increase or decrease the efficacy of drugs that rely on it to function.
If you experience diarrhea, constipation, or vomiting, you should consult a doctor immediately because most Acid reducer's side effects are mild but affect the body quickly. Some severe side effects, such as skin rashes, liver failure, and cardiac disorders, may occur in rare cases.
What is Zantac Cancer Lawsuit?
Aside from Zantac, you should be aware of Zantac cancer lawsuits. A Zantac lawsuit is a legal claim filed by people who took NDMA-contaminated Zantac and ranitidine and later developed cancer. Since discovering a possible link between Zantac use and cancer, some users have filed lawsuits against several Zantac manufacturers. Those who have filed lawsuits claim that the manufacturers were aware of the dangers of NDMA in the product but failed to warn consumers. They also claimed that the manufacturers may have designed Zantac incorrectly and purposefully refused to test Zantac products for fear of exposure.
Everyone can get support for Filing your Zantac Claim. If you or your loved ones took Zantac and believe it caused cancer, they may be able to receive compensation from the manufacturer. However, the nature of such a claim places the burden of proof squarely on your shoulders. The patient should provide evidence to the courts that their Zantac exposure caused cancer. You may want to consult with an experienced personal injury attorney to help you prove your case. Your attorney would know the best evidence to prove your claim and could fight the manufacturer's corporate lawyers on your behalf.
Closing Thoughts
Science has shown that these tablets can act as a silent killer, contributing to cardiovascular disease, cancer, type 2 diabetes, and other conditions. The fact that it kills three out of every five people worldwide. Even though some ranitidine products are still available in the market, so beware. As consumers, people all believe that the medicine introduced into the market is safe for everyone to consume, but this is not the case. Everyone is putting their own life at risk. The best thing to do if you're taking ranitidine is to consult your doctor about whether treatment is still necessary. In some cases, the benefits are likely to outweigh the risks.
