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.
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.
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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs 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
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.
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.
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.
Abilify Tardive Dyskinesia Lawsuit Cleared To Move Forward by Federal Judge September 2, 2015 Austin Kirk Add Your CommentsA federal judge has cleared the way for a lawsuit to move forward involving claims that side effects of Abilify may cause involuntary muscle movements, known as tardive dyskinesia.ย U.S. District Judge Eldon Fallon issued an order (PDF) on August 21, denying a request by the drug makers Bristol-Myers Squibb and Otsuka America Pharmaceutical Inc. to dismiss a failure to warn lawsuit filed by Cory P. Jenkins, who was diagnosed with tardive dyskinesia following Abilify use.Tardive dyskinesia is a disorder that causesย repetitive and involuntary movement, usually involving the lower face and limbs. Symptoms can include grimacing, chewing, smacking of lips, rapid eye movements and impaired finger movements. There is no known effective treatment of the disorder, and the abnormal movements can become permanent, persisting even after use of the drug has stopped.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 AboutโฆSpinal 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 COMPENSATIONAccording to allegations raised in the complaint (PDF) filed by Jenkins pending in the U.S. District Court for the Eastern District of Louisiana, he developed “chronic and continued restlessness and twitching of the upper and lower extremities, facial tics, jaw clenching and clucking, and constant eye blinking” in 2013, after taking the antidepressant.Jenkins asserted two separate theories of liability, including defective design and failure to warn about the Abilify tardive dyskinesia risk.In a motion to dismiss filed by Bristol-Myers Squibb and Otsuka, the drug makers argue that the defective design claims fail to allege that there was a safer alternative design. In addition, the defendants maintained that the failure to warn claims should be dismissed because Jenkins failed to allege that his treating physician would not have prescribed the drug if different warnings had been provided.While Judge Fallon did dismiss the design defect claim, he rejected the request to dismiss the failure to warn claim, allowing the tardive dyskinesia lawsuit over Abilify to move forward.“Plaintiff is merely required to allege that Defendants did not adequately warn Plaintiff’s treating physician and that the inadequate warning constituted the proximate warning of Plaintiff’s injuries,” Judge Fallon ruled. “[T]he Court finds that Plaintiff’s failure-to-warn claim satisfies this standard and is sufficient to survive Defendant’s … motion.”Abilify Side EffectsAbilify (aripiprazole) was approved by the FDA in 2002, and is one of the top selling drugs in the U.S., generating sales of $7.5 billion in 2013.In addition to concerns about the risk of tardive dyskinesia, Abilify has also been linked to reports of impulse control problems, including gambling addictions, sex addictions and other similar behavior that has been linked to a class of drugs known as dopamine receptor agonists.A recent study by the Institute for Safe Medication Practices, published in the medical journal JAMA Internal Medicine, found that this class of drugs was linked to impulse control problems, such as compulsive gambling, sex addiction and other issues that may have a severe impact on an individualโs life.There are six FDA-approved dopamine agonists currently on the market in the United States. The Parkinsonโs disease drugs Mirapex and Requip were most strongly linked to incidents of impulse control problems among the dopamine receptor agonists, leading to gambling addictions and hypersexuality, and even compulsive shopping. However, a safety signal was also seen for Abilify gambling and impulse control problems, with at least 37 reports found specifically involving this one medication.Researchers have warned thatย drug manufacturers failed to provide adequate warnings about the risk of impulsive behavior on the drugs, indicating that information about the risk dates back to at least 2009, when a study found that approximately 18% of patients taking a dopamine agonist for treatment of Parkinsons disease could suffer from compulsive behavior side effects.Although Abilify is a partial dopamine receptor agonists, researchers found that the same signals for gambling and other impulse control problems with Abilify were seen among users of the antipsychotic medication as well. Tags: Abilify, Antidepressant, Bristol Myers Squibb, Otsuka, Tardive Dyskinesia Image Credit: |More Abilify Lawsuit Stories Commonly Used Drugs Linked To Four Serious Adverse Side Effects: ISMP Report October 2, 2018 One-Third Of Foster Kids Prescribed Psych Drugs Without Treatment Plan, Federal Report Warns September 20, 2018 Lawsuit Over Abilify Generic Competition Filed by Otsuka Pharmaceuticals September 14, 2016 56 Comments Joan September 28, 2016 I stopped using Ability over 2 years ago and have had the most terrible jaw clenching 24 hours a day. It took me a while to realize that Ability is ? the cause. I have gone to my primary physician tried different drugs, muscle relaxers, antidepressants, as well as valium and now I take Ativan. I get Botox injections every 3 months. I still have strong muscle tension but do not clench as bad. Any type of activity makes it worse so my life has been changed forever. This has been a living hell! Merry September 11, 2016 My husband has tardivei dyskinesia terrible. His head bobs up and down,his feet do the same. He had to stop driving because his foot on the gas on off on the gas and worse the hesitation like stuck on stupid. He gets his meds from the VA had asked for 2yrs to be taken off.They got a new dr overthere and they had him try zyprexa then took him off of everything. Now he lays on the couch all day Mary Ann August 30, 2016 My 11 y/o son has autism have been on Abilify for over a year, doing better with behavior. My concern was obesity and being high risk for cardiovascular disease, so our plan was to wean him off, to make it easy for this transition, he was placed on low dose lexapro until he’s completely off, He wouldn’t sleep at night, the doctor prescribed Tenex at bedtime to decrease energy and help sleep. Now he’s presenting tar dive dyskinesia. The pediatrician thinks it’s Ability, I stopped it in a heartbeat. The dyskinesia decreased by 30-40% occurrence. On my way to bring him to a neurologist today. Donald June 6, 2016 Developed tardive dyskinesia while taking abilify. No longer taking however this drug has made me medically disabled Vicki June 2, 2016 I have tardive dyskinesia from being on Abilify for over a year. I’m no longer taking Abilify but the symptoms continue. My doctor has tried to calm it down with two different meds of which neither worked. Mary May 21, 2016 I have been on abilify. It has contributed to me getting diebetes. Tardive dyskinesia. Compulsive spending insomnia. Emotional distress. I have stopped abilify my compulsive spending is less but my uncontrollable leg movement has continuedNewer Comments 1 2 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 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. 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