Zantac Recall Cancer Support

01/11/2021

13/10/2021

30/09/2021

26/04/2021

Lots of people like you are discovering that they have been injured after taking Zantac ranitidine.

Through the breadth of these claims, we may know more soon about what kinds of cancer this drug exposes you to as well as what kind of payout you might expect after NDMA overdosing.

If you have been diagnosed with cancer, contact us to talk about your legal options. Our law firm can help you or your loved one and investigate if Zantac causes cancer.

Learn about the updated cancers associated with Zantac and randitidine use. Updated by 2021 by experienced attorneys. See if you qaulify.

21/09/2020

The Zantac recall affects about 15 million Americans who take the prescription strength drug and millions more who take over-the-counter versions, according to a report by Wired.

The FDA announced recalls for brand-name and generic Zantac because of contamination with NDMA, a cancer-causing chemical.

14/09/2020

What is Zantac? What is the legal recourse for people who developed cancer from Zantac? What are the recent developments in the Zantac lawsuits?

If you have similar questions in mind, below are some clarifications to help you out.

What Are The New Developments On The Zantac Lawsuit Cases May 20, 2020 Since its release in the market, people have taken Zantac whenever they experienced heartburn. Deemed safe, accessible, and readily available, Zantac became a first-line remedy for people. Over the years, millions of people switc...

01/09/2020

Since September 2019, there've been a steady trickle of announced recalls of popular heartburn medications after an impurity that can cause cancer was discovered in them.

You can find below the lot numbers of the voluntary recalls by date and manufacturer (or packager).

Heartburn? Better check the list for recalled Zantac and other heartburn medications.

25/08/2020

Although most drugmakers had already pulled the heartburn products months ago, the agency told consumers they should throw out any over-the-counter medications they still had.

People who take prescription forms of the drug should speak with their doctors about other options before stopping treatment.

Although most drugmakers had already pulled the heartburn products months ago, the agency told consumers they should throw out any over-the-counter medications they still had.

10/08/2020

: The Zantac lawsuits that are in federal court are now part of multi-district litigation against Sanofi and Boehringer Ingelheim.

As of the current writing, there are 291 cases that are a part of the multi-district litigation. In addition to the cases in federal court, there are also cases that have been filed in state courts throughout the country.

We anticipate that this number will rise sharply in the future given the sheer number of people who have taken Zantac over the years.

If you or a loved one have been diagnosed with cancer, you may be able to file a Zantac cancer lawsuit.

If you have long-term Zantac use, look here for information on litigation related to current lawsuits and case filings. Updated information.

13/04/2020

We are here to provide you with the latest information on recalls and pending litigation involving monetary damages.

FDA determined that the impurity (NDMA) in some ranitidine products increases over time when stored at higher than room temperatures and may result in consumer exposure to unacceptable levels of this impurity.

If you or a loved one has taken Zantac or ranitidine, and developed stomach or bladder cancer, contact us at (888) 424-5757.

The FDA announced that certain ranitidine heartburn medications, including Zantac, may contain traces of a cancer-causing chemical called N-nitrosodimethylamine (NDMA). As of now, the FDA isn't recommending people stop taking ranitidine, but those who’d like to switch medications should talk to th...

10/04/2020

The real issue with Zantac cancer lawsuits involves a chemical known as NDMA. Scientists are exploring the real impact of NDMA on health and what amounts and levels exposure to NDMA may cause cancer.

What we do know is that NDMA at elevated levels is a known carcinogen.

We are reviewing Zantac cancer cases from across the U.S. and have a team of nurses and physicians who are here to assist you with your case. We invite you to discuss your experience and your legal options with us at no cost or obligation.

Zantac Cancer Lawsuits :: What You Need to Know https://www.rosenfeldinjurylawyers.com/zantac-cancer-lawsuits.html I’m Jonathan Rosenfeld and I’m a drug reca...

07/04/2020

On April 1, 2020, the FDA requested manufacturers to withdraw all prescription and over-the-counter ranitidine drugs (Zantac, others) from the market immediately, due to the presence of a contaminant known as N-Nitrosodimethylamine (NDMA).

The FDA has not yet released the results of its testing of the heartburn medication ranitidine. The testing method used by the online pharmacy that originally alerted the FDA may have affected their results.

15/01/2020

Harvard Health suggests that people habitually taking Zantac or other forms of ranitidine to treat heartburn, acid-reflux or ulcers talk to their doctors about finding alternative treatments.

The FDA is warning consumers that Zantac may contain a cancer causing impurity

16/12/2019

We are here to provide you with the latest information on recalls and pending litigation involving monetary damages.

If you are currently taking Zantac you should speak to your doctor right away.

If you have taken the drug and developed a digestive or other type of cancer, you should consider taking immediate legal action against the drugmakers who manufactured, marketed, and sold the defective drug.

Time is of the essence, because there are statutes of limitations that apply to filing personal injury claims at both the federal and state levels.

We invite you to discuss your experience and your legal options with us at no cost or obligation.

09/12/2019

Though some over-the-counter ranitidine, sold as store brands in addition to Zantac, tested as “reasonably safe for human ingestion” of FDA standards for NDMA content, several prescription strength versions used to treat ulcers and reflux came in with unsafe numbers.

Amneal Pharmaceuticals and Golden State Medical Supply recalled prescription strength ranitidine, known as Zantac in brand name form, for having more of carcinogen NDMA than the FDA considers safe.

21/11/2019

Since the FDA announcement, lawsuits have already begun to be filed around the U.S. against the makers of Zantac and related products, including Sanofi.

Whenever there is a flurry of new litigation brought against specific defendants in different states, those early cases are often consolidated in a single state in what is known as multidistrict litigation (MDL), where they can all be heard in the same federal court before the same judge.

This is different from a class-action lawsuit and is done for efficiency in the pretrial hearing and motion process. While several class-actions have been brought over Zantac, it is too early to predict whether there will be an MDL.

The litigation is still in its early stages and there have been no settlements or verdicts related to Zantac injuries announced yet.

If you or a loved one has taken Zantac or ranitidine and developed stomach or bladder cancer, contact the defective drug injury attorneys at Rosenfeld Injury Lawyers at (888) 424-5757 to schedule a free consultation

20/11/2019

You should get in touch with your doctor for an evaluation if you experience any strange symptoms that concern you.

Anything like unintentional weight loss, bloody or tarry stools (which may indicate intestinal bleeding), symptoms of anemia like fatigue and weakness, or new abdominal pain out of proportion to what you experience on a regular basis is worth bringing up with a doctor.

If you have any additional cancer risk factors (like a history of smoking) and are really worried, it can be smart to talk to your doctor about your health as well. The same goes if you decide to switch treatment and your heartburn persists or worsens.

An epidemiologist explains.

12/11/2019

While many Americans take over-the-counter (OTC) for relief of heartburn and indigestion, prescription-strength ranitidine is sometimes used by physicians to treat and prevent ulcers in patients.

Although the initially reported that NDMA levels in the contaminated ranitidine were barely any higher than the supposedly safe amounts found in common foods, it later declared the levels to be “unacceptably high.”

However, the agency is not currently recommending that patients stop taking ranitidine products immediately, but urging patients to speak to their doctors about alternative prescription and OTC medications for their conditions.

It’s important to note that to date, brand-name (manufactured by Sanofi) was voluntarily recalled on October 18, 2019, as was the null generic version - ranitidine.