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 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
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.
Protonix May Increase Risk of Pneumonia Over Zantac for Critically Ill: Study September 22, 2009 AboutLawsuits Add Your CommentsNew research suggests that side effects of Protonix, a stomach acid reducer, may triple the risk of pneumonia for critically ill patients when compared to the competing medication, Zantac.Researchers from the Wake Forest School of Medicine in North Carolina published the results of the study last month in the medical journal Chest. The study found that both Protonix (pantoprazole) and Zantac (ranitidine), turn the stomach into a more habitable place for bacteria to grow due to their reduction of the stomachโs acid. However, Protonix, which is used more often in most hospitals, carries an increased risk of hospital-acquired pneumonia in cardiothoracic surgery patients on a breathing machine.Hospital-acquired pneumonia is a common risk for critically ill patients, particularly those on ventilators. Contraction of pneumonia puts critically ill patients at a 20 to 30 percent risk of death, and can increase a patientโs hospital stay by seven to nine days, potentially exposing them to other complications. Pneumonia usually occurs because stomach secretions have entered the lungs.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 COMPENSATIONScientists looked at 834 patient charts of hospitalized cardiothoracic surgery patients, and found that those treated with pantoprazole (Protonix) were three times more likely to contract hospital-acquired pneumonia than those given ranitidine (Zantac). The researchers found that the earlier the patient could be removed from stomach acid reducer medication, the less likely they were to contract pneumonia.Doctors commonly treat patients on ventilators for the risk of stress ulcers, which can be increased significantly while someone is on a ventilator. But researchers said that stress ulcers may not be as much of a concern for ventilator patients as it used to be, because hospitals now feed patients on breathing tubes earlier, and the food in the stomach can neutralize or reduce the effects of stomach acid.Researchers suggested that doctors elevate the heads of patients on ventilators, to reduce the chances of stomach secretions invading the lungs, and also suggested that, when stomach acid reducers are needed, doctors consider the less-powerful Zantac. Tags: Hospital Pneumonia, Protonix, Zantac Image Credit: |More Lawsuit Stories Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence August 6, 2026 Appeal Filed in Lawsuit Alleging Ultra-Processed Foods Caused Diabetes, Fatty Liver Disease for Teen August 6, 2026 Anker Power Bank Explosion Lawsuit Alleges Thermal Runaway Caused Severe Burns August 6, 2026 2 Comments linda October 21, 2014 Same here. I’ve had a cough and was diagnosed with walking pneumonia. I am coming off of this ppi. The GI doctor didn’t give my complaint any creditibility. I’m finding me a new doctor. Fred May 19, 2010 I have been on many acid reducing medication since 1986. I was put on Protonix in March, 2010 and have developed a persistent cough since taking it. This past month I was diagnosed with “walking pneumonia”, which I have never, ever had before. Maybe your article has some truth to it. Who knows?! 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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 Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: today)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: yesterday)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) Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (Posted: 2 days ago)Multiple scientific studies have linked chlorpyrifos insecticide exposure to an increased risk of Parkinson’s disease.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITParaquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Exposure Lawsuit Claims Pesticide Caused Farmer’s Parkinson’s Disease Diagnosis (07/28/2026)Chlorpyrifos Parkinsonโs Disease Lawsuit Claims Years of Insecticide Exposure Caused Neurological Side Effects (07/22/2026)
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Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: today)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)
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