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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
AFFF Lawsuit Exposure to firefighting foam chemicals may result in an increased risk of cancer for firefighters, military and airport personnel.
Side Effects of Celexa, Lexapro Linked to Heart Beat Problems: Study January 31, 2013 Irvin Jackson Add Your Comments The findings of a new study suggest that there may be a connection between side effects of certain antidepressants, such as Lexapro and Celexa, and an increased risk of abnormal heart rhythms, which could be potentially dangerous. Researchers from Massachusetts General Hospital in Boston found a dose-specific response between taking antidepressants known as selective serotonin reuptake inhibitors (SSRIs) and the length of electrical activity in the heart, known as the QT interval. A dose-specific response means that the larger the dose the more pronounced the effect, and is usually a strong indicator of a causal connection. The findings of the study were published this week in the British Medical Journal. Do You Know about… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… hair dye cancer lawsuits For Salon Professionals Hair dye lawsuits are being pursued for salon professionals who were routinely exposed to hair dye chemicals and diagnosed with bladder cancer or breast cancer. See if you qualify for a hair dye cancer lawsuit settlement. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Researchers looked at data on 38,397 patients who had an electrocardiogram to record their heart rhythms and electrical activity after taking an antidepressant or methadone between February 1990 and August 2011. The findings suggest a dose-response associations of prolonged QT interval with patients who took Celexa, Lexapro, and Elavil, but not other antidepressants. One finding that could be a possible benefit is that bupropion, sold under the brand names Wellbutrin and Zyban, appeared to shorten QT intervals, leading researchers to speculate whether it could be used to offset the side effects of the other SSRIs. FDA Warned of Celexa Heart Problems This latest research is not the first time side effects of Celexa have been linked to heart beat problems. Celexa (citalopram hydrobromide) was originally created in 1989 by Lundbeck, and is approved for the treatment of major depression. However, it is often used off-label to treat other psychological disorders. Celexa is available in brand name form or as a generic in 10 mg, 20 mg and 40 mg tablets, as well as a 10 mg/5 mL oral solution. In August 2011, the FDA issued a warning that Celexa could cause prolongation of QT intervals at high doses. The FDA warned that the condition could lead to a serious and potentially fatal abnormal heart rhythm known as Torsade de Pointes. At the time, the Celexa label was updated to include the new warning and doctors were warned not to prescribe Celexa above 40 mg per day and not to use it at all in patients with congenital long QT syndrome. The agency also called on doctors to give patients taking Celexa more frequent electrocardiogram monitoring. The results of the latest study suggest that the heart rhythm side effects may not be limited to Celexa and may be common among SSRI antidepressants, which are widely used worldwide. However, it appears not to be present with all of them, suggesting further studies need to be conducted to determine which antidepressants carry the risk and which do not. “The implications for clinicians merit careful consideration,” the researchers note. “One notable finding is that nearly one in five patients treated with these antidepressants who underwent electrocardiography had QT intervals which would be considered abnormal.” Tags: Antidepressant, Celexa, Heart Rhythm, Lexapro, SSRI Image Credit: | More Lawsuit Stories Four BioZorb Breast Tissue Marker Lawsuits Selected for Bellwether Trials April 2, 2025 Nitrous Oxide Class Action Lawsuit Filed Over Fatal Side Effects of Flavored Gas Sold In Vape Shops April 2, 2025 Artificial Stone Cutter Files Lawsuit Over Silicosis Lung Disease April 2, 2025 2 Comments Diana January 31, 2013 yes all this information is true…after years of taking Celexa and others…I developed heart disease, including A FIB etc…now I have to live with many heart medications to control my better health Vara February 14, 2013 I was prescribed Celexa in the mid-90s and round-about that time was seen in the ER for heart rhythm issues. Cardiologist ordered monitors, etc and it was determined that I’d developed supraventricular tachycardia. After the birth of my first child I was again prescribed an antidepressant, Lexapro, for post partum depression. Was on that pretty much constantly for the next 7 1/2 years except when I was pregnant. In the last two years I developed PAC’s. I had another round of monitors, etc…wondering if this is all from the use of these two drugs? 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 TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Four BioZorb Breast Tissue Marker Lawsuits Selected for Bellwether Trials (Posted: today) As new BioZorb lawsuits continue to be filed over complications with the recalled breast tissue markers, lawyers indicate they are on track for the first of four test cases to go before a jury in September 2025. 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Depo-Provera Meningioma Diagnosis Information Required To Qualify for Lawsuit: Order (Posted: yesterday) Women pursuing Depo-Provera meningioma lawsuits will have to provide documentary proof of their diagnosis and the versions of the birth control shot they received within 120 days of filing their case. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Timeline for Preparing Pilot Trial Cases Outlined by MDL Judge (03/24/2025)Women Can File Depo-Provera Brain Tumor Lawsuits Directly in MDL: Court Order (03/18/2025)75 Lawyers in Depo-Provera Lawsuits Seek MDL Leadership Roles (03/10/2025)
Cartiva SCI Lawsuit Alleges Toe Implant Worsened Pain, Decreased Range of Motion (Posted: 2 days ago) An Indiana woman has filed a Cartiva SCI implant lawsuit, indicating that the toe implant failed due to a defective design, resulting in the need for revision surgery and recommendations to permanently fuse her big toe. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Implant Injury Lawsuit Set for Trial in February 2026 (03/07/2025)Lawsuit Indicates Cartiva Implant Fails in 2 Out of 3 Patients, But Continued To Be Sold in U.S. (02/13/2025)Cartiva Toe Implant Lawsuit Filed Over Worsened Pain, Reduced Range of Motion and Need for Surgical Removal (02/07/2025)