· Shouse Law Group is a mass tort law firm that represents Zantac victims throughout the United State who took the prescription, over-the-counter, ... There is also a Zantac class action suit out of the Superior Court of Alameda, California under JCCP number 5150 (JCCP is short for Judicial Council Coordination Proceedings). Judge Evelio Grillo ...
 · Our lawyers evaluate expected settlement compensation amount in the Zantac cancer class action. Free Consultation: (800) 553-8082 ... we can give you private and free legal advice and explain your options for seeking compensation for you in a civil lawsuit. Contact a Zantac class action lawyer at 800-553-8082 or fill out this contact form ...
The FDA recalled the drug as of April 2020.Products are allowed to contain only 100 nanograms of NDMA in a daily dose. There are lawsuits against Zantac 150mg pills. A study showed that there was more than 2.5 million nanograms of NDMA in just one of these pills. Some people were told to take two pills every night for up to two months.
According to Zantac lawsuits, if you take a daily maintenance Zantac dosage of 150 mg you are being exposed to 889,000,000 ng. of NDMA a year. The lawsuits also allege that the manufacturers of Zantac knew or had a reason to know that their product, Zantac, exposes the public to unsafe levels of the cancer-causing chemical NDMA.
Based on prior settlements, we think Zantac cases in the highest settlement tiers (plaintiffs with the most types of cancer and longest use history) could get settlement payouts of around $300,000-$400,000. Second-tier cases could see Zantac lawsuit settlement amounts in the $100,000-$175,000 range.
What Proof Do I Need to Produce For a Claim? For those who have had Zantac by prescription, a history of your drug purchases should suffice. Patients who had over-the-counter Zantac recommended by their doctor should be able to prove they have used the drug by producing their medical records.
February 1, 2022 Update: A Zantac lawsuit has been filed in just over 2,000 cases. Tens of thousands of other Zantac claims have been preserved through an agreement with the filing of a Zantac lawsuit with defense lawyers and the MDL judge.
The class action suit against Zantac manufacturers in California is the first to officially schedule a trial date. Superior Court of Alameda Judge Evelio Grillo has set the start date for California Ranitidine Product Cases JCCP 5150 for October 10, 2022.
Proving use of over-the-counter Zantac is a little more difficult, but can be accomplished through receipts, notes in your medical records or even basic corroborating evidence or statements from the people you live with that support the fact that you regularly took Zantac.
Zantac Cancer Lawsuits in 2021 – It's Not Too Late to File.
Popular heartburn medication returns to market with new name - Zantac 360°™ - and new active ingredient. In April 2021, Sanofi Consumer Healthcare released a new, over-the counter (OTC) medication called Zantac 360°.
What Types of Cancer Does Zantac Cause? Zantac and other ranitidine products contaminated with NDMA, a probable human carcinogen, may be linked to many types of cancer, including bladder cancer, colon cancer and prostate cancer.
The ranitidine lawsuits are not part of a class action. Instead, these are individual lawsuits of the victim against the drugmaker. Many of the claims will join into a multidistrict litigation (MDL). This will expedite the litigation and settlement process.
Prilosec is a brand name for the generic drug omeprazole. It works by blocking the pumps in your stomach that produce acid. Zantac is a brand name for a different generic drug, ranitidine. Zantac blocks a chemical in your body called histamine that activates the acid pumps.
Famotidine and ranitidine are both in the same class of medications, H2 blockers, and work equally well to treat heartburn, acid reflux, and other stomach conditions. Famotidine does not have the same cancer risk as ranitidine, making the new Zantac 360 a safer option.
In terms of case criteria, our firm is accepting cases where the person took Zantac - or a combination of Zantac and ranitidine - for at least once...
Two claims victims can sue drug manufacturers for are 1) The drug had a defective design; and 2) The drug's labeling failed to warn about its risks.
According to online pharmacy Valisure, ranitidine's inherent instability causes a chemical reaction that produces high levels of NDMA in the digest...
Individual lawsuits. But every Zantac lawsuit will eventually be joined into an MDL -- short for multi-district litigation. MDLs are a way for cour...
On April 1, 2020, the FDA requested that all Zantac- and ranitidine manufacturers withdraw the drug. This follows a warning the FDA issued on Septe...
here were no 2021 Zantac lawsuit payouts, and none are expected in 2022 either. Settlement talks typically do not begin until some cases go to tria...
More than 10 manufacturers make prescription Zantac. And more than 20 make OTC Zantac. Manufacturers that have recalled its ranitidine products inc...
Cancer is not the only potential consequence of taking Zantac. There are at least twenty other medical conditions linked to ranitidine use: 1) Live...
Not yet. As of 2022, there is a Zantac lawsuit MDL out of the Southern District of Florida (West Palm Beach). The MDL number is 2924. The judge is...
The Zantac litigation will most likely be resolved with a global settlement of all cases. The Zantac lawsuit payouts will almost certainly be ranke...
Victims want to know when the Zantac suits will settle. A global settlement in the Zantac litigation will probably not happen soon. Big mass tort c...
Our law firm is accepting new Zantac cases for anyone who meets the following basic criteria: You took Zantac (or another ranitidine product) on a...
People taking Zantac might have unknowingly been ingesting incredibly high levels of NDMA into their system daily. Even the lower levels of NDMA fo...
Most legal experts are predicting a mass wave of Zantac lawsuits getting filed over the next few years. There are now 828 Zantac cancer lawsuits...
We do not know. This is the first MDL for Judge Rosenberg, who was appointed to the bench by President Obama in 2014. We do know that the judge mad...
Not much. You would have to fill out a comprehensive information sheet setting out your medical history. From there, for most victims, you pretty m...
Prospective Zantac plaintiffs will include anyone who regularly used Zantac and was diagnosed with cancer. The highest individual payouts in these...
A Zantac lawsuit is a legal claim for financial compensation by plaintiffs who took the heartburn medication and were later diagnosed with cancer . Zantac (and the generic version ranitidine) have been found to contain the carcinogen NDMA. Studies have linked this hepatotoxin to cancer in both animals and humans.
Zantac (and the generic form Ranitidine) have been found to contain NDMA, a powerful carcinogen that causes cancers throughout the body. A Zantac lawsuit is a legal claim for financial compensation by plaintiffs who took the heartburn medication and were later diagnosed with cancer . Zanta c (and the generic version ranitidine) ...
The FDA had found “ unacceptable amounts ” of NDMA in the ingredient ranitidine. Since then, more than a dozen pharmaceutical companies have recalled the drug. Shouse Law Group is a mass tort law firm that represents Zantac victims throughout the United States.
According to online pharmacy Valisure, ranitidine molecules are inherently unstable. When a person ingests a normal dosage of Zantac products, the active ingredient ranitidine hydrochloride converts into the carcinogen NDMA (N-nitrosodimethylamine).
According to online pharmacy Valisure, ranitidine’s inherent instability causes a chemical reaction that produces high levels of NDMA in the digestive tract. This is particularly true when nitrates are present. (Nitrates are found in foods such as bacon, hot dogs, or grilled meats.) The FDA disagrees.
These drugs are also the subject of a large set of lawsuits by cancer victims. NDMA exposure is safe in humans if limited to 96 nanograms per day. 6 But one tablet of the heartburn drug Zantac contains about 2.5 to 3 million nanograms.
On April 1, 2020, the FDA issued in effect a Zantac recall requesting that all name-brand and ranitidine manufacturers withdraw the drug. This follows a warning the FDA issued on September 13, 2019. In the interim, more than a dozen manufacturers have made a voluntary recall of their ranitidine medications:
Prescription-strength Zantac is used for the treatment of very severe heartburn and more serious conditions such as stomach/intestinal ulcers . Zantac was a very popular antacid drug since the 1980s. It was the 50th most prescribed drug with 15 million prescriptions a year.
Given the known potential of NDMA to cause cancer in lab animals, Zantac users may be at significantly increased risk of various types of cancers. NDMA ingestion from the use of Zantac can cause all types of cancer. There are some cancers scientists are more sure certain are linked to NDMA.
The researchers reported that short-term Zantac use increased the bladder cancer risk by 22 percent. Taking the drug for at least three years increased this risk to 43 percent compared to non-users. The researchers found that proton pump inhibitor use, even long-term use, was not associated with bladder cancer.
In September 2019, the U.S. Food and Drug Administration issued a public safety warning about possible cancer risks from Zantac. In the wake of the FDA safety warning, there has been a Zantac recall and ranitidine has been abruptly pulled from shelves across the country. The total number of filed MDL Zantac cancer lawsuits as of April 15, 2021, ...
NDMA is listed as a potent human carcinogen by the World Health Organization (WHO), the International Agency for Research on Cancer (IARC), the U.S. Environmental Protection Agency (EPA), and various other organizations. The CDC points out the risks of NDMA even at low doses.
Zantac ( ranitidine) belongs to a family of drugs called histamine-2 or H2 blockers. Ranitidine and other H2 blockers decrease the amount of acid produced in the stomach. H2 blockers are called "antacids" and the OTC versions are commonly used to treat and prevent heartburn (gastroesophageal reflux disease or GERD).
The pharmaceutical medication Zantac has the potential to cause cancer and other serious side-effects. You deserve justice. If you or someone you love has developed cancer after using the over-the-counter medication Zantac, please call Perenich Law Injury Attorneys as soon as possible.
Zantac is the commercial name for the medication Ranitidine. This medication is prescribed to people who suffer from overproduction of stomach acid, a condition called gastroesophageal reflux disease (GERD). Zantac can also be used to treat other gastrointestinal issues, such as heartburn, indigestion, ulcers, etc.
You may file Zantac personal injury or Zanta c wrongful death lawsuit if you or a member of your family developed cancer after taking Zantac. People who developed cancer are allowed to file a lawsuit to receive the maximum amount of compensation for their injuries.
These include: medical bills, lost wages, pain and suffering, loss of future and past earnings, temporary or permanent disability, and other compensatory damages.
Recent testing revealed that the 150 tablets contain a carcinogenic chemical that is up to 3,000 times greater than the Food and Drug Administration’s daily intake limit.
It’s chemically known as ranitidine hydrochloride and is available over the counter and by prescription. Zantac is used by many people for acid reflux, heartburn, and other gastrointestinal, throat, and stomach issues.
Additionally, for over 40 years, various studies have shown the NDMA is dangerous. Today, ND MA only has one purpose: to induce cancer in laboratory experiments. According to allegations brought forth in various Zantac lawsuits, the manufacturers of Zantac didn’t disclose to the public that Zantac, when ingested, ...
According to allegations brought forth in various Zantac lawsuits, the manufacturers of Zantac didn’t disclose to the public that Zantac, when ingested, produces very high quantities of NDMA.
In the last 40 years, numerous studies have helped make a case that Zantac causes cancer. Some of the cancers that have been associated with Zantac include: Bladder Cancer. Colon and Rectal Cancer. Esophageal Cancer. Intestinal Cancer. Kidney Cancer.
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Online resources like AllLaw are a great way to put together an initial list of candidates you might want to get in touch with when you're looking for an attorney to handle your Zantac or ranitidine lawsuit.
Whether you talk to a lawyer in person or over the phone about your potential Zantac/ranitidine case, here are some topics you might want to touch on.
Chances are a lawyer will handle your Zantac/ranitidine lawsuit on a "contingency fee" basis. This means if your Zantac case settles, or your lawsuit goes all the way to trial and you receive a judgment in your favor, your lawyer will be paid a percentage of what you receive—usually around one-third of the total.
In April 2020, the FDA ordered manufacturers to pull all Zantac and generic ranitidine off the market in the U.S. due to the risk of cancer, including all over-the-counter and prescription-strength products. The FDA warned that NDMA, a cancer-causing chemical impurity, can increase in the pills over time, or when the pills are stored ...
It is possible that class action lawsuits will be filed for everyone who purchased Zatnac or ranitidine medications that were contaminated by NDMA. However, these class actions are not designed to maximize financial compensation for people who were injured or died of severe side effects, such as cancer.
There are over a dozen recalls for over-the-counter Zantac®, generic ranitidine, store-brand heartburn medications, prescription-strength Zantac, and other products that contain ranitidine.
FDA Finds NDMA Carcinogen in Zantac. In September 2019, the FDA issued a Safety Warning for people who take Zantac® heartburn pills and generic ranitidine after a cancer-causing impurity called NDMA was detected in some medications.
In September 2019, the FDA issued a Safety Warning for people who take Zantac® heartburn pills and generic ranitidine after a cancer-causing impurity called NDMA was detected in some medications.
Bloomberg reported that Zantac tested positive for up to 3,000 micrograms of NDMA, which is significantly higher than the FDA limit of less than 1 microgram of NDMA in medicines.
These recalled drugs include Diovan, Valsartan, Irbesartan, and more.
The first Zantac class action lawsuit was filed in the Northern District of California. Four plaintiffs filed a legal complaint against Sanofi and Boehringer Ingelheim. The plaintiffs claimed the two manufacturers failed to warn consumers of the established link between ranitidine and NDMA.
Zantac and ranitidine heartburn medications are no longer available in the U.S. The recall was issued in April 2020. Retailers like Walgreens, CVS and Walmart stopped selling the drug in 2019 citing safety concerns.
Recently, tests identified a cancer-causing substance known as NDMA in the drug. NDMA was also found in ranitidine, the generic form of Zantac. Plaintiffs claim the carcinogen-containing drug caused a variety of cancers. They also allege manufacturers concealed this risk.
From 1982 to 2019, publications repeatedly highlighted ranitidine's carcinogenic potential. Drug makers did not inform consumers of ranitidine's dangers during this time period. Consumers were largely unaware of Zantac's cancer risk until Valisure, an independent pharmacy, raised the alarm.
According to one report, GlaxoSmithKline (GSK) sold $1 billion worth of Zantac as of December 1986. By 1987, Zantac accounted for a third of GSK's sales. Statista reports one form of Zantac accounted for $128.9 million in sales in 2018.
Zantac Manufacturers Should Have Warned Consumers About Cancer Risk. Zantac and ranitidine manufacturers had a responsibility to warn consumers of the drug's cancer-causing potential. However, cancer was never listed as a potential side effect on the Zantac label. Consumers might have chosen a different drug had they known ...
Diagnosed with cancer after taking Zantac? Get help from one of the most experienced lawyers in the country. Mike Papantonio is a Board Certified Trial Lawyer and senior partner at Levin Papantonio. He has received multiple Lawyer of the Year awards and is one of only 60 members of the Trial Lawyer Hall of Fame.