How Do You Qualify For Zantac Lawsuit

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Our Experts Can Help You With Zantac Lawsuit

The maker of Zantac (ranitidine) is facing a product liability lawsuit because the drug contains itrosodimethylamine (NDMA), a drug classified by the U.S. Food and Drug Administration (FDA) as a Chemical substance known as probable carcinogens by the World Health Organisation and the Environmental Protection Agency.

The Food and Drug Administration (FDA) has issued a warning that Zantac and its generic form ranitidine may cause cancer in some users. In the Zantac cases, ranitidine is a lousy drug because it contains ingredients that can form NDMA.

If you have been taking Zantac or its generic ranitidine and have developed any of the potentially related cancers, you should speak to a Zantac attorney immediately.

Call our team to hire a Zantac Cancer Lawyer today at +1 (307) 828 1476 for a free consultation.

Side-effects of Zantac

The Zantac lawsuit is filed against the manufacturers of Zantac and ranitidine by people who developed cancer from NDMA, a probable carcinogen.

Millions of people have been using Zantac for years without knowing the risks they are facing, and some users now have cancer caused by the drug. This has led to thousands of lawsuits against Zantac from people who regularly used the drug and were subsequently diagnosed with cancer.

People who have taken Zantac and filed lawsuits have reported many cases of cancer associated with the drug and NDMA. Lawyers are handling ranitidine and Zantac compensation claim list stomach, liver, and bladder cancer among the top injuries associated with NDMA contamination.

Cancer-associated with usage of Zantac

● Bladder cancer

● Prostate cancer.

● Kidney cancer

● Liver cancer.

● Stomach cancer.

● Breast cancer.

If you have one of these cancers, you must speak with an experienced Zantac attorney who can help you.

Speak with Lawyer4Help USA & determine if your cancer is a good fit to get you the compensation.

Conditions to qualify for Zantac Lawsuit:

According to Zantac’s lawyers, people must meet three conditions to qualify for a lawsuit potentially-

● proven use of Zantac

● a diagnosis of cancer

● a link between the diagnosis and Zantac 

At a minimum, people wishing to take part in the Zantac lawsuit must have taken Zantac regularly in the past and contracted a form of cancer associated with NDMA. 

Meeting these criteria makes a platform to file a lawsuit against Zantac. Keep in mind that a link between Zantac use and your cancer must be reasonably demonstrated to increase your chances of a settlement. 

Suppose you have been taking prescribed Zantac (ranitidine) for an extended period and have not been diagnosed with cancer. In that case, you can still file a Zantac class-action lawsuit to get reimbursed for the money you spent on stomach burn medication. 

Those joining the Zantac cause don’t need to prove they were directly affected by the drug, just that they bought it without being warned of any possible cancer risks. Anyone who has used Zantac and subsequently develops a severe illness can sue.

Types of Zantac Lawsuits 

There are mainly two legal actions one can take for the harm that Zantac had caused to you or your loved one’s. 

● Class Action

Thousands have joined Zantac for personal injury, wrongful death and class-action lawsuits seeking damages from drug makers that failed to detect and disclose the carcinogenic effects of drugs. 

Thousands in the U.S. have joined a lawsuit against drugmaker Zantac for failing to warn and protect consumers from the drug’s cancer-causing effects. 

● Individual lawsuit

Suppose you believe you or a family member or loved one is suffering from NDMA related cancer due to Zantac (whether or not prescribed by a doctor or over the counter). In that case, you should contact a personal injury attorney in the USA who handles Zantac MDL cases.

Compensation and result for Zantac lawsuit 

After taking ranitidine-based Zantac, people diagnosed with cancer can sue for compensation, which includes lost wages, medical bills, and pain and suffering. 

In addition to the FDA, drug agencies worldwide have also begun recalling a popular heartburn drug. 

On September 20, 2019, the Italian Medicines Agency announced that all versions of Zantac containing the active ingredient manufactured by Saraca Laboratories Ltd. in India would be withdrawn. The Italian government has also banned other Zantac products by testing if different versions are infected.

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