Propecia litigation

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  1. Den-ver XenForo Moderator

    Propecia litigation


    The national law firm of Parker Waichman LLP has long and successfully fought for its clients over problems involving defective drugs and injuries associated with these drugs. Defective drug issues relate to recalled drugs, drugs that were not adequately tested for all of their potential side effects, manufacturing errors, dosage mistakes, inadequate warnings and mislabeling. This issues may arise with prescription drugs or over-the-counter (OTC) drugs. Food and Drug Administration (FDA) before it reaches the consumer. Pharmaceutical companies manufacture and market hundreds of new drugs annually. Even with this regulatory oversight, according to the U. Centers for Disease Control and Prevention (CDC) pharmaceutical drugs kill over 40,000 people every year. In 2011, it was reported that prescription drug deaths outnumbered traffic fatalities in the U. Also, recent studies noted by the CDC estimate that more than 50 percent of the drugs marketed to the American consumer have damaging effects, despite testing and FDA regulation. Parker Waichman is renowned in the industry as experts in defective drug litigation. Our attorneys are well versed in all areas involved in this type of litigation and have a long track record of great success on behalf of our clients. This site has been designed as an aid to the bench, bar and public for the dissemination of information concerning mass tort cases throughout the State of New Jersey that are centralized in Middlesex Vicinage, Atlantic Vicinage, and Bergen Vicinage by the New Jersey Supreme Court. Please visit our "Frequently Asked Questions" page to learn more about mass tort management, and about the information that will be posted here. Also available is the NJ Multicounty Litigant (Non-Asbestos) Resource Book. The public and the bar are welcome to offer comments and suggestions, as well as information and documents that may be appropriate for posting on this web site. [email protected] immediately, Track Assignment Notices (TANS) will no longer be used in Multicounty Litigation cases. The identity of the assigned judge and team leader for each case appears on this website.

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    Litigation over Merck’s hair-loss drug Propecia—which plaintiffs allege can cause sexual dysfunction and emotional disorders—is still in its early stages and is rapidly evolving, said John F. Romano of the Romano Law Group speaking at the HB Litigation Conferences Propecia Litigation Update teleconference on Oct. 26. Propecia lawsuit allegations In addition to lasting sexual disorders, the alopecia treatment has also been linked to other adverse symptoms, including depression, cognitive impairment, anxiety, male breast cancer and prostate cancer. Drug Manufacturer, Pharmacist, Physician Responsibility. Prior to submitting a drug for approval by the FDA, drug manufacturers must ensure proper clinical testing is conducted. Drug makers must also include any potential adverse reactions and warnings on the drug label so that patients, their caretakers, and their physicians are appropriately aware of all the risks tied to the medication.

    Email Contact Form If you would like us to review your case or have questions about our firm and services, please submit this email Contact form. One of our staff members will contact you within 48 hours of submission. John Romano, partner in the Romano Law Group, was recently inducted into The Trial Lawyer Hall of Fame. The Trial Lawyer Hall of Fame was established by The Trial Lawyer to recognize and honor remarkable American lawyers who have committed a lifetime of service to the American public. Read More John Romano was recently awarded the honor of the Florida Justice Association’s Jon E. John Romano (2nd from left) was honored by the Florida Justice Association with the Eagle Centurion Award for his substantial lifetime commitment to the Endowment... Read More The Romano Law Group was recently recognized in the Second Annual Daily Business Review Florida Verdicts Hall of Fame Awards for their $3,171,000 verdict in the wrongful death case Swain v. For several years, the Daily Business Review (DBR) and its sister company Verdict Search have... Read More Eric Romano was recently selected by his peers for inclusion in 22nd Edition of The Best Lawyers in America 2016 in the field of Personal Injury Litigation – Plaintiffs. Since 1983, Best Lawyers© has been a respected peer-review publication. It is a significant honor to be listed among The Best... Editors carefully fact-check all Drugwatch content for accuracy and quality. The 2015 settlement was one of the largest Big Pharma settlements in U. Drugwatch’s legal partners are no longer taking Actos cases. Drugmaker Takeda Pharmaceuticals agreed to pay $2.4 billion to settle about 9,000 lawsuits over life-threatening injuries caused by its Type 2 diabetes drug Actos. Editors carefully fact-check all Drugwatch content for accuracy and quality. Without admitting guilt — and continuing to stand by the effectiveness of Actos — Takeda settled around 9,000 claims for $2.4 billion in 2015. A federal court that once coordinated thousands of Actos lawsuits stopped accepting Actos cases in April 2018. This includes peer-reviewed medical journals, reputable media outlets, government reports, court records and interviews with qualified experts. More than 10,000 lawsuits accused Takeda Pharmaceuticals of failing to adequately warn patients of the risk of bladder cancer and other side effects associated with its Type 2 diabetes drug Actos. This includes peer-reviewed medical journals, reputable media outlets, government reports, court records and interviews with qualified experts. At one point, more than 5,000 federal cases were part of the Actos multidistrict litigation (MDL) in the U. District Court for the Western District of Louisiana. MDLs are how federal courts manage large numbers of lawsuits that involve the same or similar issues. Another 4,500 Actos lawsuits were filed in various state courts, including Illinois, Pennsylvania, California and West Virginia.

    Propecia litigation

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  5. More than 1,000 men have filed lawsuits that accuse Merck & Co. Inc. of failing to adequately warn consumers and members of the medical community that the hair-loss drug Propecia may cause long-term sexual dysfunction problems that continue long after men stop taking the drug.

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