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.
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.
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.
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.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
Roblox Lawsuit Families are filing Roblox lawsuits after children were targeted by predators for grooming, sextortion, sexual abuse, or exploitation on the platform. Learn who qualifies, what cases allege, and how to file a confidential claim.
Ocaliva Lawsuit Ocaliva lawsuits are being investigated for users who experienced liver failure, cirrhosis progression, transplant, or death after taking the drug, alleging that Intercept Pharmaceuticals failed to warn about the risk of dosing toxicity and accelerated liver damage.
ByHeart Formula Recall Lawsuit Parents are now filing ByHeart recall lawsuits alleging that contaminated infant formula caused botulism and other serious illnesses after the company failed to prevent or warn about dangerous manufacturing lapses.
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.
Roundup Carcingenic Findings Defended by World Health Organization’s IARC February 9, 2018 Irvin Jackson Add Your Comments An international group of widely respected and independent cancer researchers is defending their decision to warn about the carcinogenic risks with Roundup and other glyphosate-based weedkillers, fighting back against recent attacks by Monsanto and regulators some say are in the manufacturer’s pocket, and House Republicans. In a letter (PDF) by Christopher Wild, director of the World Health Organization’s International Agency for Research on Cancer (IARC), the group directly answers and deconstructs recent claims made by Monsanto and its supporters, which attacked the independent cancer groups March 2015 warning about the link between glyphosate and non-Hodgkin’s lymphoma, suggesting unknown nefarious purposes and bad science. The letter was read into the record by U.S. House Representative Suzanne Bonamici of Oregon, during a hearing of the House Science, Space and Technology Committee, where Republicans recently criticized IARC and threatened it’s funding due to the decision to warn people that Roundup and similar weed killers could cause cancer. ROUNDUP LAWSUITS Were you or a loved one exposed to RoundUp? Exposure to RoundUp has been linked to an increased risk of developing Non-Hodgkin’s Lymphoma and other cancers. RoundUp cancer lawsuits are being actively investigated. Learn More SEE IF YOU QUALIFY FOR COMPENSATION ROUNDUP LAWSUITS Were you or a loved one exposed to RoundUp? Exposure to RoundUp has been linked to an increased risk of developing Non-Hodgkin’s Lymphoma and other cancers. RoundUp cancer lawsuits are being actively investigated. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The February 6 hearing was the latest attack on IARC, which has come under barrage by allies of Monsanto after its conclusions regarding Roundup cancer risks. The comments also come after a controversial decision by the U.S. Environmental Protection Agency (EPA), which refuted the IARC’s findings, maintaining that glyphosate does not cause cancer. However, a growing body of independent research and evidence has highlighted close ties between Monsanto and regulators, suggesting that the multinational agrochemical company has exercised undue influence over both U.S. and European regulators and government officials. Monsanto’s own internal records have revealed that the company was the ghostwriter for a number of studies claiming glyphosate was safe, secretly co-writing some safety reviews by regulators, and allegedly suppressing or re-writing safety reviews. In his testimony, House Chair Lamar Smith, of Texas, claimed that Wild was either afraid to show up at the hearing or had no defense for the IARC’s methodologies or actions. Smith failed to mention that Wild had apparently written a response to the Committee’s concerns weeks ago, and addressed claims against the IARC point-by-point. The letter did not come to light until Congresswoman Bonamici had it read into the official record of the hearing. “Since the evaluation of glyphosate by the IARC Monographs Program in March 2015, the Agency has been subject to unprecedented, coordinated efforts to undermine the evaluation, the program and the organization. These efforts have deliberately and repeatedly misrepresented the Agency’s work,” the letter states. “In response to the misrepresentations, the Agency has sought to provide a clear account of its actions, including keeping its governing bodies informed of developments.” The letter notes that many of the Monsanto and GOP arguments questioning the IARC’s findings parroted talking points in articles written by Kate Kelland, a Reuters reporter who critics warn appears to have close ties to Monsanto, and a March 2015 article that was published in Forbes, which later removed that article from their website and ended their relationship with a reporter after discovering that the article had actually been ghostwritten by Monsanto. Wild’s letter targets the arguments point by point, explaining how the IARC did not, and probably could not, have edited parts of the glyphosate Monograph to achieve a particular purpose. The letter notes that a draft copy of the monograph, which appeared to be more favorable to Monsanto, was actually written by Monsanto. Kelland then compared the two drafts and claimed the Monsanto draft was the original and that the IARC had then edited it to make it unfavorable to glyphosate. Wild also noted that IARC staff do not draft or revise the Monograph text, but instead that is done by an the independent, international working group of researchers from various disciplines from across the globe, including even researchers from the EPA. The letter further refutes claims that the IARC specifically left out the findings of a study that indicated that glyphosate did not increase the risk of cancer. Wild noted that the IARC only used published and peer-reviewed studies for their evaluations. The data Monsanto and the GOP claim was purposely kept out of the IARC’s findings, from the Agricultural Health Study (AHS), were only in draft form at the time. The IARC does not use non-peer-reviewed, unpublished, draft data in its reviews, similar to numerous scientific panels and agencies worldwide. The 10-page letter appears to address every scientific question raised about the IARC’s Roundup cancer determination in a point-by-point format, backed up with ample links to publicly available articles and documents. Monsanto’s Influence Revealed By Ongoing Roundup Cancer Litigation The hearing and recent EPA actions have led to further questions raised following the revelation of the “Monsanto Papers” which is the name given to a number of damning internal documents from Monsanto, which were revealed as part of the ongoing U.S. litigation against Monsanto by farmers, landscapers and other individuals who indicate they developed non-Hodgkin’s lymphoma following Roundup exposure. The memos and emails suggest that the company has known that its herbicide might be dangerous for years, put out ghostwritten studies that were falsely portrayed as the work of independent scientists, and unduly influenced regulators in the U.S. and Europe to avoid any indication that Roundup is not safe. The company even went as far as writing some parts of the safety reviews for regulators, and asked them to squash government inquiries that they could not write themselves, some of the documents suggest. Throughout the U.S., several thousand Roundup lawsuits have been filed against Monsanto by farmers, landscapers, agricultural workers and others regularly exposed to Roundup, alleging that they may have avoided a diagnosis of non-Hodgkins lymphoma or other cancer if warnings had been provided by Monsanto. Since October 2016, all federal cases have been consolidated for pretrial proceedings as part of an MDL, or multidistrict litigation, which is centralized before U.S. District Judge Vince Chhabria in the Northern District of California. As part of the coordinated litigation, it is expected that a small group of bellwether trials will be prepared for early trial dates to help gauge how juries may respond to certain evidence and testimony that will be repeated throughout the cases. However, if Monsanto fails to reach Roundup settlements or another resolution for the failure to warn cases, hundreds of individual lawsuits may eventually be remanded back to the federal courts where they were originally filed for an separate trial dates. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Cancer, Congress, Glyphosate, Herbicide, Monsanto, Roundup, Weed Killer More Roundup Lawsuit Stories Roundup Safety Study Retracted Decades After Publication December 8, 2025 Monsanto Roundup Settlement Avoids $2B Payout in Non-Hodgkin’s Lymphoma Lawsuit November 18, 2025 Bayer’s Roundup Lawsuit Payouts Result in Another $1.37B in Reserves August 4, 2025 0 Comments X/TwitterThis field is for validation purposes and should be left unchanged.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 Term Δ MORE TOP STORIES Dupixent Cancer Lawsuit Filed Over Cutaneous T-Cell Lymphoma (CTCL) Diagnosis (Posted: today) An Illinois woman diagnosed with stage IV cutaneous T-cell lymphoma (CTCL) after two years of Dupixent injections has filed a lawsuit against the drug manufacturers. MORE ABOUT: DUPIXENT LAWSUITLawyers Propose Dupixent Lawsuit Be Set for Trial After Dec. 6, 2027 (12/11/2025)Dupixent CTCL Lawsuit Filed Over Diagnosis of Both Mycosis Fungoides and Sezary Syndrome (12/05/2025)Drug Makers Must Respond to Dupixent Lawsuit Over Lymphoma Diagnosis by Jan. 7, 2026 (12/02/2025) Ozempic, Wegovy Vision Loss Lawsuits Sent to Stomach Injury Judge, as Separate MDL (Posted: yesterday) All Ozempic and Wegovy vision loss lawsuits have been consolidated before the same federal judge overseeing related claims alleging stomach paralysis linked to the medications. MORE ABOUT: OZEMPIC LAWSUITOzempic, Mounjaro Side Effects May Increase Risk of Cough: Study (12/03/2025)Sudden Ozempic Blindness Reports Raise Concerns Over NAION Side Effects (11/26/2025)Ozempic, Similar Drugs Linked to Higher Risk of GI Side Effects: Study (11/21/2025) Depo-Provera Meningioma Warning Update Approved by FDA, As Lawsuits Move Forward (Posted: 2 days ago) The FDA has approved an update to the Depo-Provera drug label to include a warning of the risks of meningioma. MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Alleges Depo-Provera Neurological Symptoms Were Result of Meningioma (12/12/2025)Court To Weigh Evidence That Depo-Provera Causes Meningioma Tumors in Mid-2026 (12/08/2025)Depo-Provera Lawsuit MDL Status Hearings Scheduled Throughout 2026 (12/01/2025)
Dupixent Cancer Lawsuit Filed Over Cutaneous T-Cell Lymphoma (CTCL) Diagnosis (Posted: today) An Illinois woman diagnosed with stage IV cutaneous T-cell lymphoma (CTCL) after two years of Dupixent injections has filed a lawsuit against the drug manufacturers. MORE ABOUT: DUPIXENT LAWSUITLawyers Propose Dupixent Lawsuit Be Set for Trial After Dec. 6, 2027 (12/11/2025)Dupixent CTCL Lawsuit Filed Over Diagnosis of Both Mycosis Fungoides and Sezary Syndrome (12/05/2025)Drug Makers Must Respond to Dupixent Lawsuit Over Lymphoma Diagnosis by Jan. 7, 2026 (12/02/2025)
Ozempic, Wegovy Vision Loss Lawsuits Sent to Stomach Injury Judge, as Separate MDL (Posted: yesterday) All Ozempic and Wegovy vision loss lawsuits have been consolidated before the same federal judge overseeing related claims alleging stomach paralysis linked to the medications. MORE ABOUT: OZEMPIC LAWSUITOzempic, Mounjaro Side Effects May Increase Risk of Cough: Study (12/03/2025)Sudden Ozempic Blindness Reports Raise Concerns Over NAION Side Effects (11/26/2025)Ozempic, Similar Drugs Linked to Higher Risk of GI Side Effects: Study (11/21/2025)
Depo-Provera Meningioma Warning Update Approved by FDA, As Lawsuits Move Forward (Posted: 2 days ago) The FDA has approved an update to the Depo-Provera drug label to include a warning of the risks of meningioma. MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Alleges Depo-Provera Neurological Symptoms Were Result of Meningioma (12/12/2025)Court To Weigh Evidence That Depo-Provera Causes Meningioma Tumors in Mid-2026 (12/08/2025)Depo-Provera Lawsuit MDL Status Hearings Scheduled Throughout 2026 (12/01/2025)