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.
Fosamax Lawyers in Femur Fracture Litigation Appointed to Leadership Roles July 28, 2011 Staff Writers Add Your CommentsU.S. District Judge Garrett E. Brown, Jr., who is presiding over all federal Fosamax femur fracture lawsuits, has appointed a number of lawyers to serve in leadership roles in the recently formed multidistrict litigation (MDL).These attorneys will perform certain actions during the coordinated pretrial litigation that will benefit all plaintiffs who have filed a lawsuit over a fractured femur from Fosamax, a popular osteoporosis medication manufactured by Merck & Co.In May, the U.S. Judicial Panel on Multidistrict Litigation ordered that all complaints involving fractured bones on Fosamax will be transferred to Judge Brown in the U.S. District Court for the District of New Jersey as part of an MDL, or multidistrict litigation. All of the lawsuits involve similar allegations that side effects of Fosamax increase the risk of atypical femur fractures, which can occur with little or no trauma at all.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 COMPENSATIONPlaintiffs argue that Merck failed to properly research the medication or adequately warn consumers. The FDA required new warnings about the risk of Fosamax thigh bone fractures in October 2010, and a growing number of Fosamax lawyers throughout the United States have been reviewing and filing lawsuits since then on behalf of individuals who suffered a sudden femur fracture while taking the medication.Although Fosamax is designed to strengthen the bones and reduce the risk of fractures associated with osteoporosis, long-term use of the medication has been linked to a risk of these rare, spontaneous fractures of the femur. Consumers are now warned that they should seek immediate medical attention if they experience groin pain, which may occur several weeks before a complete fracture while on Fosamax.At the time the MDL was formed, there were 36 Fosamax fracture lawsuits pending in federal district courts throughout the United States. Since that time, about 24 additional cases have been transferred to the MDL. In addition, a larger number of cases have been filed in state court in New Jersey and other states throughout the United States.In a Case Management Order issued late last month, Judge Brown appointed the law firms of Carella, Byrne, Cecchi, Olstein Brody & Agnello, P.C. and Seeger Weiss, LLP to the position of co-liaison counsel. On July 14, he appointed 10 attorneys to form a plaintiffs steering committee that includes James E. Cecchi, Wesley Chadwick Cook, Christopher A. Seeger, Mark P. Robinson, Jr., Fred Thompson, Victoria J. Maniatis, Frank E. Piscitelli, Jr., Leonard A. Davis, Arnold Levin, James R. Dugan and David J. Dickens.The plaintiff liaisons will perform services that benefit all Fosamax fracture lawyers representing plaintiffs, such as maintaining a document depository and complete records of all documents served in the cases, as well as receive and distribute pleadings, motions and orders.The MDL will have no impact on Fosamax lawsuits over jaw problems, known as osteonecrosis of the jaw, which will remain centralized as part of a different MDL in the U.S. District Court for the Southern District of New York, before U.S. District Judge John F. Keenan.There are currently more than 900 Fosamax jaw lawsuits consolidated in New York, as part of an MDL that was established in August 2006. Fosamax fracture lawsuits were previously excluded from that MDL, because it was determined that the evidence of general causation leading to femur fractures would likely differ substantially from cases dealing with jaw bone damage. Tags: Fosamax, Fosamax Fracture, MDL, Merck, New Jersey Image Credit: |More Fosamax Lawsuit Stories Fosamax Fracture Lawsuits Dismissed Again, After Judge Rules FDA Rejected Label Warning Change March 24, 2022 Zometa Side Effects Increase Risk of Osteonecrosis of the Jaw: Study January 14, 2021 Study Questions Whether Fosamax And Similar Bone Drugs Provide Benefits After Seven Years of Use December 10, 2020 0 Comments CommentsThis 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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