Who Can Join The Zantac Class Action Lawsuit? - Zanes Law in Fayetteville, North Carolina

Published Oct 13, 21
4 min read

Zantac Lawsuit Update July 2021 - Console And Associates in Fort Collins, Colorado



Depending on the strength of the reaction, the outcome may be NDMA. During digestion, Zantac will naturally come into contact with water inside the user, triggering the NDMA-forming process. Jet engine fuel Industrial-grade lubricants Gasoline refining processes Cigarette smoke This information is available to the public and certainly should have been known by Big Pharma while making Zantac.

The alternative is that they were grossly negligent in its manufacturing process and never realized that ranitidine could cause the formation of NDMA. In either circumstance, the negligence may be enough to hold the companies liable for wrongdoing and damages suffered by Zantac users. What Can NDMA & Zantac Cause? The harm caused by prolonged Zantac use may be varied.

Zantac Lawsuit Update July 2021 - Console And Associates in Fort Collins, ColoradoZantac Cancer Lawsuits - Morgan & Morgan Law Firm in Fort Collins, Colorado

It is, however, known to be destructive to the liver, kidneys, and lungs due to repeated exposure. Bladder Cancer Breast Cancer Colorectal Cancer Esophageal Cancer Kidney (Renal) Cancer Liver Cancer Lung Cancer Pancreatic Cancer Prostate Cancer Stomach Cancer It is also believed that NDMA can cause irregularities in the blood.

Zantac Lawsuit Class Action - Oppenheim Law in Fort Collins, ColoradoZantac Lawyers - Rutter Mills in Fort Collins, Colorado

Can You Sue Zantac’s Manufacturers? Have you been diagnosed with one of the aforementioned cancers after using Zantac regularly and as prescribed? You might have an opportunity to bring a lawsuit against Sanofi and Boehringer with the assistance of our dangerous drug lawyers in Michigan. Medical expenses, including future treatments Lost, missing, or reduced wages due to illness Pain and suffering Lessened enjoyment of life As a consumer, you deserve to be able to trust the products you use, especially when they can be purchased off-the-shelf or over-the-counter.

South Florida Court Dismisses Civil Rico Claim In Zantac Case in Fort Collins, Colorado

Start your fight with the guidance and representation of our highly experienced lawyers from Goodman Acker, P.C.

Home » New Class-Action Lawsuit Filed Against Zantac Manufacturers Because of Potential Cancer Risk On September 26, 2019, five plaintiffs jointly filed a class-action lawsuit against Sanofi-Aventis LLC, makers of the stomach-acid medication, Zantac (ranitidine). They’ve also named as defendants Boehringer Ingelheim Pharmaceuticals, Inc., which owned the U.S. rights to Zantac and manufactured and distributed the drug from October 2006 to January 2017, after which Sanofi acquired the rights.

The Environmental Protection Agency (EPA) has classified NDMA as a probable human carcinogen. FDA Warns of Potential Contamination with Zantac and Generic Ranitidine In September 2019, manufacturer Sandoz initiated a recall of ranitidine capsules (generic Zantac) after testing discovering NDMA in batches of the drug. The FDA notified healthcare providers and the public of the recall on September 24, 2019, stating a nitrosamine impurity had been discovered in the recalled medicine.

Ranitidine and Zantac are available as over-the-counter and prescription drugs. They are histamine-2 blockers, which work by decreasing the amount of acid in the stomach. They are used to treat conditions like heartburn, acid indigestion, sour stomach, ulcers, and gastroesophageal reflux disease (GERD). Patients were advised to follow the recall instructions provided by Sandoz, as well as those provided by Apotex Corp., which initiated its own ranitidine recall on September 25, 2019.

Zantac® Lawsuit? - Indiana - Ken Nunn Law Office in Fort Collins, Colorado

Independent Testing Shows High Levels of NDMA in Zantac Valisure, an online pharmacy that stakes its reputation on testing the drugs it sells, submitted a citizen petition to the FDA in June 2019 requesting that the agency take action after Valisure detected levels of dimethylformamide (DMF) in blood pressure drugs.

Valisure noted that since pharmaceutical manufacturing switched to the use of DMF as a solvent, nitrosamine impurities started showing up in heart disease drugs like valsartan. Valisure reported that it found high levels of NDMA in all lots of ranitidine tested, across multiple manufacturers of ranitidine products. Valisure submitted another citizen petition to the FDA, noting that the ranitidine molecule itself contains both a nitrite and a dimethylamine (DMA), which are known to combine to form NDMA.

Valisure’s testing of Zantac detected 2,511,459 ng of NDMA per 150 mg tablet of Zantac. In a follow-up test of Zantac in conditions simulating the human stomach, the quantity of NDMA was as high as 304,500 ng per tablet. The plaintiffs in the class-action lawsuit allege that the defendant Zantac manufacturers knew or had reason to know that Zantac exposed users to unsafe levels of NDMA, since numerous scientific studies indicated it did, yet they failed to disclose the risk and continued to sell the product to the public.

Facts You Need To Know Regarding Zantac Lawsuit in Fort Collins, ColoradoEverything You Should Know About The Zantac Class Action ... in Fort Collins, Colorado

Zantac Lawyer Have you or a loved one taken Zantac? Zantac may cause cancer and those who have taken Zantac or ranitidine may be at risk. If you or a loved one have suffered from cancer potentially due to Zantac (ranitidine), you may be entitled to compensation. For a FREE, no-obligation consultation with an experienced Zantac lawyer, please call There are no attorney fees unless we recover compensation for you.

Navigation

Home