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.
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 Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment October 2, 2026 Paraquat Settlement Offers Rejected by Hundreds of Parkinsonโs Disease Plaintiffs October 2, 2026 Walmart Expert Grill Brush Recall Impacts 4.4 Million Over Wire Bristle Ingestion Risk October 2, 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 Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: yesterday)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026) Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: 2 days ago)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026) Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: 3 days ago)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)
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