Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working
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.
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.
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.
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.
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.
Essure Birth Control Problems Result in Consumer Reports Guide August 18, 2017 Irvin Jackson Add Your Comments Consumer Reports has published a guide for women considering the permanent Essure birth control procedure, warning about the hidden risks and serious Essure problems that have been reported in recent years. The consumer guide was posted to the watchdog group’s website on August 17, amid increasing concern about the safety of the metal coil implant, which is designed to provide permanent sterilization. The group warns women that they may suffer severe pain, weight gain, migraines, heavy bleeding, and autoimmune system problems following Essure birth control procedures. According to Consumer Reports, thousands of women have reported serious side effects and complications after being implanted with Essure. Data suggests that three to four percent of women who receive the implant suffer complications. However, given the widespread use of the device, that has resulted in nearly 17,000 adverse event reports filed with the FDA, half of which indicate that women had to undergo surgery as a result, which often involve a full hysterectomy. Learn More About Essure Implant Lawsuit Problems with Essure birth control implant may cause painful complications. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Essure Implant Lawsuit Problems with Essure birth control implant may cause painful complications. Learn More SEE IF YOU QUALIFY FOR COMPENSATION The Consumer Reports guide includes a list of expert questions women should ask before undergoing the sterilization procedure, such as what the health risks are, how experienced is the doctor performing the procedure, whether the doctor will remove the device if there are problems, and what other birth control options are available. The guide also includes a list of necessary information for those women considering having the implant removed. Essure Complications Essure procedures involve the placement of coils in the fallopian tubes, which are designed to cause scar tissue to form and prevent pregnancy. In November 2016, the FDA added a black box warning label to Essure implants, which is the strongest that the FDA can require a medical device carry. The black box came after a large number of independent experts recommended that additional information be provided about the Essure procedure problems experienced by many women who received the coils, including perforation of the uterus and fallopian tubes, pain and allergic reactions. The new warnings also inform women that if Essure needs to be removed, it must be done through a surgical procedure. Women who undergo the birth control procedure in the United States are now be presented with a patient checklist, which is designed ensure that they are aware of the potential side effects of Essure coils. Approximately 750,000 women worldwide have been implanted with the device, and Bayer estimates that 70% of those have been implanted in women in the U.S. Due to the manufacturers failure to warn about the risk of problems in recent years, thousands of women are now pursuing Essure lawsuits, indicating that they may have avoided serious complications if information had been disclosed to consumers and doctors. Tags: Bayer, Birth Control, Essure More Essure Lawsuit Stories Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working November 1, 2023 Progress of Essure Birth Control Implant Post-Marketing Study “Inadequate,” FDA Warns Bayer October 11, 2022 85% of Bayer Essure Adverse Event Reports Submitted Last Year Linked to Device Removal: FDA March 16, 2022 0 Comments 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 Suboxone Injury Lawyers Reappointed to Leadership Roles in Federal MDL (Posted: today) A federal judge has confirmed the reappointment of more than two dozen Suboxone injury lawyers to serve in leadership positions representing plaintiffs for another year. 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Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working November 1, 2023
Progress of Essure Birth Control Implant Post-Marketing Study “Inadequate,” FDA Warns Bayer October 11, 2022
85% of Bayer Essure Adverse Event Reports Submitted Last Year Linked to Device Removal: FDA March 16, 2022
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