Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Chlorpyrifos Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
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.
Side Effects of Dilantin, Tegretol, Other Epilepsy Drugs Linked to Fracture Risk January 12, 2011 Staff Writers Add Your CommentsEpilepsy drugs like Dilantin and Tegretol may be linked to an increased risk of fractures in older patients, according to the findings of a new study. Researchers from Canada found a correlation between the use of epilepsy drugs and an increased risk of fracture in every major antiepileptic except Depakote and other valproic acid-based drugs. Dilantin was found to carry the highest risk of fractures. Their findings were published in this month’s issue of the Archives of Neurology.The researchers conducted a cohort study of 15,792 people age 50 and older who suffered nontraumatic wrist, hip and vertebra fractures between 1996 and 2004. They found that the risk of fracture increased between about 24% for clonazepam-based drugs, like Klonopin and Valpax, and 91% for Dilantin. They found no increased risk in those taking Depakote.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know About…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONMuch of the recent attention on antiepileptic drugs by scientists has focused on suicide risks and birth defects. In 2008, the FDA conducted a meta-analysis that led to a 2008 decision requiring all epilepsy drugs to carry a suicide risk warning. But some researchers have said that risk appears to be limited to newer epilepsy drugs while older drugs, like Depakote, Neurontin and Lamictal, appeared to have no increased risk of suicide.Dilantin (phenytoin) is an antiepileptic drug manufactured by Pfizer. Mylan makes a generic version called Phenytek which is considered bioequivalent.In November 2008, the FDA issued a warning about a risk of Stevens-Johnson syndrome from Dilantin and its generic equivalents. It has also been linked to a rare condition known as Purple Glove Syndrome.Stevens-Johnson Syndrome (SJS) is a painful and debilitating reaction that has been linked to several medications. It can cause the skin to burn, producing blisters, severe rashes and the skin may begin to 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 in a hospital Intensive Care Unit (ICU) or Burn Unit is often required, and the conditions can be fatal in many cases. Tags: Birth Defect, Depakote, Dilantin, Epilepsy, Epilepsy Drug, Fractures, Lamictal, Neurontin, Pfizer, Phenytek, Phenytoin, Purple Glove Syndrome, Stevens-Johnson Syndrome, Tegretol, Toxic Epidermal Necrolysis Image Credit: |More Lawsuit Stories AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 3 Comments Eileen August 14, 2011 I have been taking Tegretol plus Lamictal for 13 years. If I take my meds and eat Pizza, Cheese Pizza or others, I become dizzy within 15 minutes after eating it. This is if I take the Meds right before or after or for up to 1 hr. before or 1 hr. after. When I say dizzy, I mean to the point I cannot stand up. I need to be held up and walked to my bedroom and sleep it off for at least 6 to 8 hrs, and then I get around with minimal dizziness and feel unbalanced. Anyone out there have this reaction? John July 12, 2011 I am a 56 year old male with temporal lobe epilepsy since age 26. I’ve been taking Phenytoin for use as a anti-convulsant since 1982. In 1985 I suffered a factured ankle, and in 2005 the other ankle was fractured. Well, my question is why in respects to male fertility is or was nothing ever posted on the “Precautions or Warning lnformation. Many studies I’ve found dating back to 1998 showed spermatogenesis and testicular atrophy in juvenille and adult male rats and dogs. I am now on Depakote for a mood disorder I have and for the seizures. Further compounding the male fertility problem which very well may be the underlining cause of the “mood-disorder” I have or have developed over these last three decades. Man, my youg adult-hood got hijacked and now at middle age the Urologists tells me I’m all good despite my direct questioning Physicians over the years of the possibility of there being a connection to my infertilitty with the Dilantin and now Depakote. Where’s the warning? Since my twenties my libido changed drastically while on phenytoin and as I recall I seemed to be stronger and more alive when I went off it for awhile. “Knowing but not knowing” at the time that it was the right thing to do. I think I should have been told of the risks and given an optional drug. Pamela January 15, 2011 I am a 43 year old female.I have taken Dilantin and Zonegran for several years,not sure if they had any part in my knee injury.I go in Monday to have surgery on my knee.God Bless Us All.always pam 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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: yesterday)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 2 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)
Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 3 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)