Monday, February 26, 2024

Can Zantac Cause Thyroid Cancer

Why Should I Hire Hach & Rose Llp

What Types of Cancer Have Been Linked to Zantac?

Hach & Rose, LLP is an accomplished product liability firm with over 100 years of combined experience. We fight hard for our clients, and we get results: we have won over $400,000,000 for our clients. At Hach & Rose, LLP, we believe that forming respectful, honest, and compassionate relationships with our clients allows us to achieve the best results possible. Not only do we work tirelessly for you, but we treat you like family. Our clients are consistently satisfied with the work we perform, how we walk them through the process step-by-step, and our responsiveness to any questions along the way.

As a patient who was prescribed Zantac, or family member, you may be unfamiliar with the potential risks of the drug and related ramifications. Rest assured that our attorneys have the resources necessary to thoroughly investigate any dangers related to the drug, medical causation, compliance with FDA regulations, any alleged wrongdoing, and all other factors that could affect your case. Our attorneys are well versed in class action lawsuits and will fight aggressively on your behalf.

We understand that you may be worried that hiring an attorney will be too expensive. At Hach & Rose, LLP, we work on a contingency-fee basis, which means that we take a percentage of your overall settlement or verdict at the end of your case. We charge no bills or fees along the way. If you dont win your case, then you dont owe us any money at all.

Which Generic Zantac Is Recalled

Many of the manufacturers, packagers, distributors, and other parties involved in the production of generic ranitidine products issued voluntary recalls of some or all of these medications or otherwise halted distribution and sales of the prescription and over-the-counter drugs. These companies that have announced recalls include:

  • Sandoz, part of Novartis AG
  • Northwind Pharmaceuticals
  • Appco Pharma LLC

Additionally, Mylan Pharmaceuticals recalled H2 blockers with nizatidine as the active ingredient, after investigations suggested that this medication could contain a similar NDMA impurity.

The FDAs April 2020 request that manufacturers immediately remove all ranitidine products from the U.S. market extends to all manufacturers of generic Zantac and to all lots, batches, dosage amounts and formulations. At this time, all generic forms of Zantac have effectively been removed from the market due to FDAs findings regarding the investigation of NDMA impurities.

Zantac Prescription And Serious Side Effects Statistics

According to the FDA Adverse Event Reporting System , they received a total of 73,240 cases with a negative effect of Zantac since 1983.* This includes:

  • 55,891 serious cases
  • 66 percent of the total cases were linked to cancer

*This number combines cases where the patient had multiple adverse reactions. For example, if a patient reported three different reactions, we counted them just once

In 2018, 18,739,686 people in the United States were prescribed Zantac. The same year, 1,094 cases involving Zantac were reported to the FDA. There were 316 cases that reported that the drug was ineffective. At this time, only two cancer cases were identified.

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What Researchers And Cancer Patients Are Claiming About Ranitidine

Often, cases of drug contamination involve a mistake made somewhere in the process of manufacturing, processing, or packaging the drug or its ingredients. In other instances of NDMA drug contamination in recent years, the contamination can be traced back to a company or facility. Usually, only certain batches of the medication are contaminated.

That isnt the case with Zantac. Instead, it appears that, under certain conditions unfortunately, the ones usually found in the human body or those the drug is exposed to during distribution the active ingredient in Zantac, ranitidine, may create NDMA as a byproduct of chemical reactions that occur as the medication breaks down.

If thats true, the problem would be far larger than a few, or even a few million, lots of Zantac. The danger would exist across all lots of heartburn medications using the active ingredient ranitidine, from all manufacturers, in all forms and dosages, produced in all areas and, quite possibly, over the entire time a span of decades that the drug has been on the market.

How Much Is A Zantac Lawsuit Worth

Zantac Esophageal Cancer  Everything You Need to Know

In Arkansas, you can recover compensation for economic and non-economic damages during a Zantac claim. Economic damages involve financial losses, such as medical expenses, disability accommodations, and lost wages and benefits. On the other hand, non-economic damages refer to the physical and emotional pain and suffering that you endured.

There are several factors that influence the value of your settlement:

  • The severity of your cancer
  • The types of medical care that you need to treat your cancer
  • The length of time you spend away from work
  • Whether the cancer takes away your ability to work

Your Arkansas Zantac lawyer from Estey & Bomberger, LLP can evaluate your product liability claim and help identify all possible paths to compensation. An attorney experienced in dangerous drug lawsuits can then calculate an accurate estimate of your settlement, helping you avoid insufficient offers.

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Free Legal Consultation For Zantac Ranitidine Users With Cancer

If you or a loved one used the heartburn medications Zantac or ranitidine and were diagnosed with breast cancer, thyroid cancer, bladder cancer, prostate cancer, or other types of cancer, you may qualify to file a lawsuit and receive compensation. The first step in taking legal action is to speak with an attorney who can help answer your questions about the process of filing a lawsuit.

For more information about whether you may qualify to file a Zantac or ranitidine lawsuit, contact the lawyers at Hissey, Mulderig & Friend to schedule your free legal consultation. You can reach us by calling toll-free at , or by filling out our free case evaluation form located on the right side of this page.

After we receive your message, one of our staff members will contact you to help you schedule your free attorney consultation.

Questions To Ask The Doctor

  • What treatment do you think is best for me?
  • Whats the goal of this treatment? Do you think it could cure the cancer?
  • Will this treatment affect my ability to have children? Do I need to avoid pregnancy for a while?
  • Will treatment include surgery? If so, who will do the surgery?
  • What will the surgery be like?
  • Will I need other types of treatment, too? Whats the goal of these treatments?
  • What side effects could I have from these treatments?
  • What can I do about side effects that I might have?
  • Is there a clinical trial that might be right for me?
  • What about special vitamins or diets that friends tell me about? How will I know if they are safe?
  • How soon do I need to start treatment?
  • What should I do to be ready for treatment?
  • Is there anything I can do to help the treatment work better?
  • Whats the next step?

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Can I Sue The Makers Of Zantac For Developing Cancer

Cancer patients and their families should speak to a Zantac cancer lawyer right away if they:

  • Regularly used ranitidine, whether over-the-counter or by prescription
  • Took name-brand Zantac or a generic formulation made by any pharmaceutical manufacturer
  • Used any form of ranitidine, including tablets, caplets, and syrups or oral solutions
  • Used any dosage of ranitidine, including 75 mg, 150 mg, 300 mg, and 15 mg/mL liquid formulations

If you took Zantac and developed cancer, you may have the right to pursue a claim for compensation for damages that include the medical expenses you have incurred and the pain and suffering you have been through.

Zantac Attorney In Massachusetts


The U.S. Food and Drug Administration has asked stores to stop selling the heartburn drug Zantac after finding that a cancer-causing contaminant in the product can build up over time and when stored at higher than room temperatures.

The FDA advised individuals who take over-the-counter forms of the drug, also known as ranitidine, to stop taking any tablets or liquid that they have and not buy more. Individuals who take a prescription form of the medication should consult with their physician before discontinuing use, the agency said.

If you or a loved one has been diagnosed with cancer after regular use of Zantac or other ranitidine medications, you could be eligible for compensation.

Zantac Recall Law Firm in Boston

The Jeffrey Glassman Injury Lawyers in Boston has years of experience in dealing with these types of claims and recovering maximum compensation for our clients and their families. Our dangerous medications attorneys arent afraid to take on big drug companies and get you the compensation that you deserve.

Our lawyers are actively investigating Zantac claims and keeping abreast of developments in this rapidly evolving area of litigation. Contact our law office today for a free and confidential consultation. There are no out-of-pocket fees unless we recover money for you.

Jeffrey Glassman Injury Lawyers Can Help You with Your Zantac Cancer Claim

Other research suggests that NDMA causes liver damage as well as numerous types of cancer, including:

  • Testicular cancer

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How Much Money Will I Recover

The amount of compensation you receive will depend on a variety of factors. In general, plaintiffs in product liability lawsuits are eligible to seek compensation for two kinds of damages: economic and non-economic damages. Economic damages are measurable, should be easily verified, and represent a monetary loss. Non-economic damages are subjective and not related to direct monetary losses.

Your economic damages are the expenses you incurred as a result of your cancer. These are medical bills, including emergency room visits, hospital stays, surgery, cancer treatment, specialist visits, prescriptions, physical therapy, and the cost of transportation to medical appointments. Economic damages also include lost wages if your cancer has made you unable to work, as well as future lost income if your cancer has impacted your ability to work in the future.

Non-economic damages can be harder to quantify but are just as significant. They include non-pecuniary losses, such as pain, suffering, emotional trauma and anguish, loss of enjoyment of life, and loss of consortium . In some states non-economic damages are referred to as pain and suffering. In order to make the case that you deserve compensation for non-economic damages, its a good idea to keep a journal in which y

What These Zantac Studies Cumulatively Show

Bigger picture, the latest studies demonstrates that the medical litigation on the association between ranitidine and Zantac continues to support plaintiffs attorneys theories of liability in the Zantac litigation of the health complications with Zantac.

Ultimately, even before the recall, there was information out there to warn of the ranitidine risk and allow patients to pursue ranitidine alternatives.

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Should I Consider A Lawsuit

People who have been diagnosed or developed cancer after taking Zantac prescription or over-the-counter formulations or other medications containing ranitidine may be eligible for compensation. Eligibility for filing a Zantac lawsuit include those who used Ranitidine regularly for over 60 days and were diagnosed with:

What Do Plaintiffs Lawyers Think About The Expected Settlement Amounts Of Zantac Lawsuits

Should You Take Zantac While Pregnant?

We talk above generally about the expected settlement amounts in the Zantac lawsuits. This is another way of asking the question. What are Zantac lawsuit lawyers thinking?

Our lawyers frequently talk to other attorneys about what they think about what the expected settlement compensation payouts might be in the Zantac lawsuits. There are some mass torts out there that plaintiffs attorneys almost universally believe are slam-dunk cases that will have a very high settlement value.

So what about Zantac? There is no consensus among Zantac lawyers on what the settlement amounts might be in these cases. Some attorneys are very high on these cases. Our law firm believes Zantac compensation will be high in terms of jury payouts and settlement amounts in the Zantac class action.

Other Zantac lawyers are less impressed with what they think these cancer lawsuit settlement amounts will be in these cases. This is true even for some attorneys who are advertising online and on television. One reason why there are so many Zantac lawsuits is that the tolling agreement and short-form complaint make these cases easy and cheap to file. So lawyers who are not gung ho on the viability of these lawsuits are still bringing suits because the effort required to file a claim is so small.

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What About Other Treatments I Hear About

When you have cancer you might hear about other ways to treat the cancer or treat your symptoms. These may not always be standard medical treatments. These treatments may be vitamins, herbs, special diets, and other things. You may wonder about these treatments.

Some of these are known to help, but many have not been tested. Some have been shown not to help. A few have even been found to be harmful. Talk to your doctor about anything youre thinking about using, whether its a vitamin, a diet, or anything else.

Who Do You Sue In A Zantac Cancer Lawsuit

Generally, a Zantac cancer lawsuit argues that the company that made the drug was negligent in producing a dangerous product and failing to warn consumers of the risks. The defendant, or the party you would be suing in your Zantac cancer lawsuit, would be the manufacturer of the medication you took.

If you took prescription Zantac, the manufacturer would be GlaxoSmithKline. Consumers who took OTC Zantac may sue Sanofi, Boehringer Ingelheim, Pfizer, or some combination of these manufacturers, depending on when they took the medication since the rights to make over-the-counter name-brand Zantac have been transferred between these companies since the drug came onto the U.S. market.

Patients and consumers who took generic Zantac would need to pursue a claim against the company that manufactured the generic product they took. If you used more than one generic ranitidine formulation over the years or switched from name-brand Zantac to a generic version, you may have claims against multiple manufacturers.

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When Was Zantac Recalled

Because of the links between ranitidine and unacceptable levels of NDMA, Zantac and other drugs that contained ranitidine were voluntarily recalled in 2019. First pharmacies like CVS, Walmart, and Walgreens pulled the drugs from their shelves, including Zantac as well as their own versions of ranitidine drugs. Later that same year, the manufacturers of Zantac and the other ranitidine-based drugs voluntarily recalled their own products.

As of 2019, the FDA was investigating ranitidine, but had not yet issued any kind of recall or had even advised patients taking Zantac or another version of the drug to stop taking it, issuing only a warning in the meantime. It wasnt until 2020 that the FDA concluded its investigations and found that there was an unacceptable amount of NDMA in ranitidine and issued its own recall.

The Winding Road To Recall

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Valisure first began looking closely at ranitidine after the infant daughter of a company co-founder was prescribed generic ranitidine syrup. As concern grew about the NDMA in ranitidine, Valisure filed the petition on Sept. 9, 2019, asking the FDA to recall the drug. Their request was followed by this chain of events:

  • The FDA issued a safety announcement Sept. 13, 2019, stating that it had learned some ranitidine medicines contain NDMA. In this, it did not call for people to stop taking the drug, but it suggested those taking the prescription form should talk to their doctors if they wanted to discontinue it and those who wished to stop the OTC versions could consider other heartburn medicines.
  • Many manufacturers began voluntary recalls.
  • In November 2019, the FDA compared levels of NDMA in ranitidine to levels that people would expect when eating grilled or smoked meats.
  • On April 1, 2020, the FDA requested removal of all ranitidine products from the market. It noted that the NDMA levels rise over time when the medication is stored at higher than room temperature.

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How Is It Treated

Anaplastic thyroid cancer requires immediate treatment since it spreads quickly. For about half of people who receive a diagnosis, the cancer has already spread to other organs. In these cases, treatments focus on slowing its progression and keeping you as comfortable as possible.

Unlike some other types of thyroid cancer, anaplastic thyroid cancer doesnt respond to radioiodine therapy or thyroid-stimulating hormone suppression with thyroxine.

Your doctor will discuss with you all the available treatment options. They can help you choose one thats best suited for both your condition and personal preferences.

New Studies Confirm Zantac Ranitidine Cancer Risks

Two new studies published by the online pharmacy Valisure have confirmed that patients who use the heartburn drug Zantac and its generic equivalent, ranitidine, face an increased risk of developing cancer. The increased risk is due to a carcinogenic chemical that forms in patients stomachs when Zantac or ranitidine are ingested. Both heartburn medications were recalled in 2019 after Valisure alerted the public that patients who used the drugs were at risk of developing cancer due to their chemical contamination.

Hundreds of lawsuits against the manufacturers of Zantac and ranitidine have already been filed by patients diagnosed with cancer after using these drugs. Experts have predicted that thousands of cases involving the two heartburn drugs could eventually be filed.

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What Is In Zantac That Causes Cancer

NDMA is the main chemical in Zantac that is known to cause cancer in animals and probably in humans.

Zantacs relationship with NDMA is unique. Out of all the drugs that FDA has found to be contaminated with NDMA including valsartan, losartan and metformin ranitidine has been the only medication in which levels of the carcinogen may actually increase over time as the drug sits on the shelf.

FDA has found N-nitrosodimethylamine levels in some ranitidine products increase with time and temperature posing a risk to consumers, and therefore the agency has requested the withdrawal of all ranitidine products from the U.S. market. Source: U.S. Food and Drug Administration

The pharmacy Valisure first brought the problem to the FDAs attention in June 2019, and it filed a citizens petition in September 2019 requesting that the FDA recall all ranitidine products.

The pharmacys research found that ranitidine was unstable and could generate very high levels of NDMA. Ranitidine contains a dimethylamine and a nitrite, chemicals that combine to form NDMA.

Studies performed by Stanford University and other academic groups revealed NDMA levels far above the FDAs current daily acceptable intake limit of 96 ng. In fact, the Stanford study suspected that ranitidine could form millions of ng of NDMA.

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