Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
AngioDynamics Port Catheter Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Zantac Cancer Risk Results in DOJ Probe of GlaxoSmithKline and Sanofi SA August 3, 2020 Irvin Jackson Add Your Comments GlaxoSmithKline and Sanofi face a Justice Department probe that is looking into what the drug makers knew about the risk of cancer from Zantac, and when it may have discovered that the main ingredient in the recalled heartburn drug concerns to the carcinogenic chemical byproduct N-nitrosodimenthylamine (NDMA). Zantac (ranitidine) was aggressively marketed for decades as a safe and effective treatment for heartburn, including both prescription and over-the-counter versions of the treatment, which have generated billions in sale. However, after an independent pharmacy discovered late last year that pills contained high levels of NDMA, Zantac recalls have been issued for most versions of the medication. NDMA used to be a chemical byproduct of making rocket fuel in the early 1990s. However, today, its only use is to cause cancer in animals as part of laboratory experiments. ZANTAC LAWSUITS Did you or a loved one take recalled Zantac? Side effects of Zantac may increase the risk of cancer, due to chemical impurities found in the heartburn drug. Learn More SEE IF YOU QUALIFY FOR COMPENSATION ZANTAC LAWSUITS Did you or a loved one take recalled Zantac? Side effects of Zantac may increase the risk of cancer, due to chemical impurities found in the heartburn drug. Learn More SEE IF YOU QUALIFY FOR COMPENSATION In filings to the Securities and Exchange Commission (SEC), Sanofi and GlaxoSmithKline announced they are under investigation by the Department of Justice. “On 18 June 2020, the Group received a Civil Investigative Demand (CID) from the US Department of Justice (DOJ) seeking information related to Zantac pursuant to the False Claims Act,” GlaxoSmithKline wrote in it’s Q3 report to the SEC. “The Group is co-operating with the DOJ to provide this information. Additionally, on 18 June 2020, the New Mexico Attorney General filed a lawsuit against multiple defendants, including GSK, relating to Zantac and other products containing ranitidine.” Reports indicate that the DOJ is investigating whether the companies failed to adequately inform regulators about the potential presence of the known carcinogen in Zantac. While FDA standards have established that maximum human daily exposure to NDMA should be only 96 nanograms, testing by the independent pharmacy Valisure found some 150 mg Zantac pills contained more than 3 million nanograms of NDMA. Exposure to the Zantac ingredient has been linked to reports of breast cancer, kidney cancer, leukemia and other cancers, raising widespread concerns among long-term users of the drug. Valisure is an independent online pharmacy that tests drugs thoroughly before sending them to customers. In September 2019, the pharmacy filed a citizen’s petition with the FDA, calling for Zantac recalls after detecting high levels of N-Nitrosodimethylamine (NDMA) in every batch of Zantac it tested. After determining there was no way to reliably determine which pills were contaminated, the FDA decided all manufacturers must issue Zantac recalls for ranitidine-based drugs on April 1, decades after the drugs were introduced and after millions of Americans were exposed to the chemicals which may have caused the development of breast cancer, testicular cancer, kidney cancer, bladder cancer and other injuries. Hundreds of Zantac lawsuits are now being pursued throughout the United States by former long-term users of the medication who indicate they have developed cancer from the heartburn drug. However, it is widely expected that tens of thousands of claims will eventually be involved in the litigation, given the widespread use of the medication. To deal with the increasing complaints being filed throughout the federal court system, the U.S. Judicial Panel on Multidistrict Litigation recently ordered all Zantac claims be centralized and consolidated in the U.S. District Court for the Southern District of Florida, where the litigation will be overseen by U.S. District Judge Robin L. Rosenberg during coordinated discovery and pretrial proceedings. Tags: Cancer, Drug Recall, GlaxoSmithKline, Heartburn, Heartburn Drug, NDMA, Sanofi, Zantac More Zantac Lawsuit Stories Zantac Cancer Lawsuits Continue To Be Filed More Than 5 Years After Recall June 18, 2025 Jury Hears Zantac Cancer Evidence in Illinois Trial Against Boehringer Ingelheim February 5, 2025 Zantac Bladder Cancer Lawsuit Trial Ends With Hung Jury in California November 22, 2024 0 Comments Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Lawsuit Pre-Settlement Funding and Loans Must Be Disclosed Under Court Order (Posted: today) A U.S. District Judge has ordered women involved in Depo-Provera lawsuits to inform him of any third-party pre-settlement loans they take out, as predatory interest rates may force them to reject settlement offers. 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