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.
Cymbalta Stevens-Johnson Syndrome Lawsuit Filed Against Eli Lilly January 18, 2012 Staff Writers Add Your Comments A Kansas woman is has filed a product liability lawsuit against Eli Lilly and Co. after suffering a dangerous and disfiguring skin reaction, known as Stevens-Johnson syndrome, which was allegedly caused by side effects of Cymbalta.ย Nanci Matos, filed the Cymbalta lawsuit in the U.S. District Court for the District of Kansas on January 6. According to the complaint, Matos alleges that she developed Stevens-Johnson syndrome from Cymbalta, a popular antidepressant and anti-anxiety medication. Learn More About Stevens-Johnson Syndrome Lawsuit Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Stevens-Johnson Syndrome Lawsuit Learn More SEE IF YOU QUALIFY FOR COMPENSATION Matos began taking Cymbalta in November 2009. By December, she indicates that she started to show signs of a skin reaction and was hospitalized in January 2010. Stevens-Johnson Syndrome (SJS)ย is a reaction that can be caused by some medications, where the skin begins to burn from the inside out, producing blisters, severe rash and the skin may separate from the body. When the skin lesions affect more than 30% of the body, the condition is typically referred to as toxic epidermal necrolysis (TEN). Treatment for SJS or TEN typically involves inpatient care at a hospital Intensive Care Unit (ICU) or Burn Unit, and the conditions can be fatal in many cases. Matos’ Stevens-Johnson syndrome lawsuit claims that Eli Lilly failed to adequately warn doctors and patients that Cymbalta side effects could cause dangerous skin reactions. According to the lawsuit, the FDA asked the company as early as 2007 to investigate potential link between Cymbalta and skin reaction problems, but Eli Lilly allegedly ignored that request and a number of other warnings by experts until September 2011, when the Cymbalta label was updated to include a warning of SJS and other skin reaction side effects. Matos accuses Eli Lilly of strict liability, negligence, breach of warranty, misrepresentation, fraud and violations of consumer protection laws. She seeks damages for disfigurement, pain, suffering, mental anguish, embarrassment, shame, loss of enjoyment of life, loss of consortium and other injuries. Tags: Cymbalta, Eli Lilly, Product Liability, SJS, Stevens-Johnson Syndrome, TEN, Toxic Epidermal Necrolysis Image Credit: | More Stevens-Johnson Syndrome Lawsuit Stories Azithromycin Lawsuit Claims Side Effects of the Antibiotic Resulted in SJS/TEN Symptoms February 13, 2026 Ibuprofen Stevens-Johnson Syndrome Side Effects Left Brazilian Woman Comatose for 17 Days May 10, 2024 HIV May Cause Some Cases of Stevens-Johnson Syndrome Without Drug Interaction: Study December 13, 2023 5 Comments LYNN November 15, 2013 Was prescribed Cymbalta for depression, took Cymbalta for years. A few months ago I was prescribed over the recommended dosage. Woke up in massive pain 9-5-13. At Emergency they found blood in my spine, did CT scan and found blood around the brain. Transported to UC Davis Med Center. Originally diagnosed with brain aneurysm. Several surgeries no aneurysm found. Surgeons think it was a brain bleed resulting from serotonin reuptake inhibitor syndrome caused by Cymbalta. The brain bleed caused a brain stroke. Went through horrible jerking and sleeplessness for weeks in intensive care unit at UC Davis as a result of the withdrawals from Cymbalta. I was in UC Davis Medical Center in NSICU for about 6 weeks and was not released for the hospital until October 22nd. I have found that studies have shown that Cymbalta causes unusual ‘Bleeds’ and believe that Cymbalta caused the brain bleed that resulted in my stroke. I have suffered from depression all my life and have now been informed by the doctors that because of my condition caused by Cymbalta I will never be able to take any type of anti-depressant for the rest of my life which will result in ruining the quality of my life Kenneth August 12, 2013 My doctor increased my Cymbalta from 90mg in the morning to 60mg twice a day in the morning and at bedtime since the increase bilster like forms started on my skin all over my body. It has now reached a point where it is very painful to walk or due regular activity. I am very scared that this with get worse as I also have diabetes type 1, I also have phybromigia . Jim February 26, 2013 MY wife seriously disabled by Cymbalta recently rhonda October 21, 2012 I commend each and everyone of you for telling your stories of the adverse affects of these prescription drugs. The pharm companies are no better than the meth pusher on the corner. I encourage everyone to report side affects of all drugs to the fda via their website. I look forward to the day the ceo’s of the pharm co’s are charged in the criminal court for the deaths that have resulted from their pills. Tresa October 5, 2012 Lets talk for a minute about LOSS OF ENJOYMENT OF LIFE,SHAME< EMBARRASSMENT,MENTAL ANGUiSH,PAIN,SUFFERING, AND ABOVE ALL LOSS OF LIFE…YES I SAID LOSS OF LIFE…. not only my husbands, but of mine… are these ppl ever going to compinsate for the loss of my husbands life in turn THE LOSS OF MY LIFE AS I knew it…..what a joke this med is and for Lily to continue to pass this out is a crime. CommentsThis 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 Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (Posted: today) A group of about 70 Depo-Provera meningioma lawyers have been reappointed to key leadership roles in the litigation, as thousands of women seek compensation for brain tumors they say were caused by the birth control shots. 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