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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Side Effects of Ambien, Xanax, Valium May Increase Risk of Respiratory Cancer: Study June 30, 2015 Irvin Jackson Add Your CommentsNew research suggests that some popular sleeping aids may increase the risk of respiratory cancer, raising concerns about the safety of widely used medications like Ambien, Xanax, Valium and others.ย In a study published earlier this month in the medical journal Sleep Medicine, researchers from the Norway Institute of Public Health found that the use of benzodiazapines and a class of drugs known as z-hypnotics could triple the risk of cancers that affect the respiratory system, such as lung cancer.Researchers looked at data from the Finnish Cancer Register and the Drug Prescription Register of Finland, evaluating data on about 30,000 subjects, including more than 5,000 with cancer diagnosed from 2002 through 2011.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 the findings, the use of sleeping pills like Ambien, Lunesta, Valium, Zanax and Ativan appear to increase the risk of all types of cancers slightly, but the greatest and most significant increased risks came from lung cancers and similar ailments. While the risk of all cancers was increased by just under 20%, the risk of respiratory cancer rocketed up 347%, according to the findings.Researchers called for further studies to examine the links between cancer, sedatives and sleeping pills.The findings come a little more than a month after the Institute for Safe Medication Practices (ISMP) raised questions about the safety of Ambien and similar sleeping drugs, suggesting that clinical trials used to obtain FDA approval for the medications do not actually match how the drugs are used. The ISMP found that consumers often use the medications far longer than is recommended, and they are often used by those with mental illness or taking other psychoactive drugs.According to the ISMP report, the U.S. Centers for Disease Control and Prevention (CDC) found that Ambien and its generic zolpidem equivalents were the drug most linked with emergency room visits, according to adverse event data received by the FDA. According to the report, there are an estimated 10,2112 emergency department visits each year linked to Ambien use, with 25% of those requiring the person be hospitalized.The findings are similar to those of another study published last year by the Substance Abuse and Mental Health Services Administration (SAMHSA), which found that emergency room visits involving side effects of Ambien increased from 21,824 in 2005 to 2006, up to more than 42,000 in 2009 to 2010.In 2014, the FDA received 1,030 serious adverse event reports where Ambien was the primary or secondary drug suspected of causing the problem.Lingering Ambien Side EffectsAmid increasing use of sleeping pills, concerns have emerged about problems that may be caused by lingering effects of the medication the next day, including drowsy driving accidents and other issues caused when individuals remain dangerously impaired the next day. Several reports suggest that women may be more susceptible to these problems, but all individuals required to perform tasks requiring high levels of alertness may be at risk.In January 2013, the FDA issued a safety alert indicating that recommended Ambien doses should be lowered, cutting the recommended dose for women in half, and indicated that doctors should prescribe all patients the lowest dose possible to treat the symptoms.New warnings for Ambien, Zolpimist and other zolidem sleeping pills were approved by the FDA in May 2013, indicating that users should not drive or engage in other activities requiring mental alertness the next day after taking the medication.In May 2013 the FDA approved a new warning label for sleeping pills like Ambien and Zolpimist. The warnings recommended lower doses to reduce the risk of experiencing lingering side effects the following morning after taking the drug.A study published in August 2013 backed the FDAโs decision to cut doses of Ambien and other sleeping drugs, concluding that individuals taking the sleeping pills may not recognize their level of impairment the following day before driving or completing other complex tasks.Researchers said levels of the drugs remain in the blood stream for more than an eight-hour sleep and stay high in the morning. This impairs the ability to perform certain tasks, but also impairs the users judgment whether they are still under the influence of the drug.According to a report published in the British Medical Journal in 2012, people who take Ambien or other sleeping pills are five times for likely to die within two and a half years than someone who does not take sleeping pills. The study also revealed sleeping pill users may also face an increased risk of developing cancer.Health experts estimate six to 10 percent of the adult population used sleeping pills in 2010, making them one of the most widely used classes of drugs in the U.S.According to the ISMP there were 40 million dispensed prescriptions for Ambien in 2013, the vast majority of those were for the pills in their generic form. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Ambien, Cancer, Lunesta, Lung Cancer, Sleeping Pill, Valium, Xanax Image Credit: |More Lawsuit Stories Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 HeartMate II Wrongful Death Lawsuit Claims LVAD Implant Caused Thrombosis April 16, 2026 Video Game Addiction Lawsuit Claims Devs Use Behavioral Manipulation on Kids April 16, 2026 2 Comments Deborah July 20, 2021 In these studies, how long did the people take zanax and at what dosage did they take? Kelly December 6, 2016 Increased headaches and memory loss EmailThis 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026) Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026) WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)
WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)