Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
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.
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.
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.
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.
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.
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.
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.
At Least 8 Lawsuits Over Oxbryta Filed Against Pfizer, Global Blood Therapeutics Lawsuits have been brought in California state court and federal court, claiming the recalled sickle cell disease drug caused serious health complications for former users. March 14, 2025 Irvin Jackson Add Your Comments In response to a federal judge’s request for information about the number of Oxbryta lawsuits filed over the recalled sickle cell disease drug, lawyers have submitted a report indicating that there are two complaints pending in the federal court system, and at least another six brought in California state court, each raising similar allegations that former users suffered severe side effects and injuries. Oxbryta (voxelotor) was introduced by Global Blood Therapeutics in 2019, as the first medication to treat the root cause of sickle cell disease, which it was supposed to do by improving hemoglobin levels in the body and helping the blood cells retain more oxygen. The company, and the drug, were purchased by Pfizer in 2022, who continued to sell the expensive treatment for about $88,000 per year for each patient receiving the treatment. However, following numerous reports of users experiencing painful sickle cell complications and deaths, Pfizer announced a global Oxbryta recall in September 2024, after determining that risks associated with the treatment outweigh the potential benefits, discontinuing the drug only five years after it hit the market. Oxbryta Lawsuit Were you prescribed Oxbryta? Oxbryta lawsuits are being filed for sickle cell disease patients who developed vaso-occlusive crises (VOCs), strokes and other side effects caused by recalled Oxbryta. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Oxbryta Lawsuit Were you prescribed Oxbryta? Oxbryta lawsuits are being filed for sickle cell disease patients who developed vaso-occlusive crises (VOCs), strokes and other side effects caused by recalled Oxbryta. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Since the recall, a steady stream of lawsuits have been brought, alleging that side effects of Oxbryta actually cause users to face a higher rate of sickle cell disease-related incidents, known as vaso-occlusive crises (VOC). Vaso-occlusive crises occur when the red blood cells block blood flow, and the tissues become deprived of oxygen. This can cause an inflammatory response, which can lead to symptoms like pain in the chest, back and limbs, as well as fever. Patients often have to be hospitalized and can suffer kidney failure and stroke. Additionally, many patients can die following a vaso-occlusive event. In February, U.S. District Judge Trina L. Thompson in the Northern District of California scheduled an Oxbryta lawsuit for trial in summer of 2027, involving claims brought by Tirrell Allen, and asked lawyers involved in the case to submit a report outlining information about the status of others filed to date. In a joint statement (PDF) submitted on March 7, the parties indicated that at least eight Oxbryta injury lawsuits have been filed, including one other claim beside the one brought by Allen in the federal court, and six in state courts. On March 5, Judge Thompson issued an order (PDF) calling for the one other federal Oxbryta lawsuit, which is a joint claim brought by four different former users, to be reassigned to her as a related case. Judge Thompson has scheduled the Allen trial for June 2027, and while the outcome of that trial will not be binding on other Oxbryta lawsuits, it is likely to be closely watched to see how the jury responds to evidence and testimony that will likely be repeated throughout a large number of claims. The outcome could help the parties reach an Oxbryta settlement agreement for former users of the discontinued drug. In the joint statement submitted last week, the parties indicated that they are already discussing a mediator and schedule for Oxbryta settlement talks, which may result in a quick resolution to the litigation. Tags: Oxbryta, Oxbryta Recall, Pfizer, Sickle Cell, Stroke 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. More Oxbryta Stories Oxbryta Settlement Reached by Pfizer To Resolve Vaso-Occlusive Crisis Lawsuit November 6, 2025 EU Confirms Oxbryta Risk of Sickle Cell Disease Complications, Death Outweigh Benefits October 30, 2025 Lawsuit Indicates Oxbryta Side Effects Put Child in ICU October 7, 2025 0 Comments LinkedInThis 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 Lawsuit Claims Spinal Cord Stimulator Battery Problems Resulted in Removal of Boston Scientific Device (Posted: today) A Florida man has filed a lawsuit alleging that battery-related malfunctions in a Boston Scientific spinal cord stimulator caused severe pain and shocking sensations, which required repeated reprogramming attempts that failed, requiring permanent removal. 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EU Confirms Oxbryta Risk of Sickle Cell Disease Complications, Death Outweigh Benefits October 30, 2025
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