US Drug Watchdog Now Offers The Contacts Of National Caliber Women Attorneys For Victims Of A Transvaginal Mesh, Tape, Or Sling Failure & Urges The FDA Do Something Now

The US Drug Watchdog has dramatically grown their national initiative focused on helping women recipients of a failed transvaginal mesh, tape, or sling, because there could easily be thousands of victims. According to the New York Times, "In 2010, about 185,000 US women underwent procedures in which mesh was implanted vaginally to treat urinary incontinence-that was just one year." The US Drug Watchdog says, "Transvaginal mesh, tape, or sling failure occurs when the mesh fails to bind to a woman's pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvaginal mesh, tape, or sling may start to poke its way through the vaginal wall and protrude out of the vaginal tissue." The US Drug Watchdog's national initiative is designed to assist any women in the US, who is a victim of a transvaginal mesh, tape, or sling failure, and the group will provide all women victims with the specific contacts of national caliber attorneys-who are all women. For more information women, who are now victims are urged to call the US Drug Watchdog anytime at 8660714-6466. http://USDrugWatchdog.Com

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If the US FDA, the doctors, and these device makers do not get real attentive to these victims immediately-we will make this mess so expensive-the phrase costs beyond comprehension will have to be redefined

(PRWEB) November 09, 2012

The US Drug Watchdog says, "Because a transvaginal mesh, tape, or sling failure can be such a complicated and very delicate issue for a woman victim, we have designed our Victims Initiative around the core concept that women victims will get access to the highest caliber national attorneys-who are all women." The US Drug Watchdog does not believe a woman victim of a transvaginal mesh failure would want to share this type of information with a male attorney. As a background the transvaginal mesh products were designed for women, who were suffering from pelvic organ prolapse, and or stress urinary incontinence. The procedure to install a transvaginal mesh was supposed to be minimally-invasive. The US FDA is now saying transvaginal mesh failures are causing complications in patients such as erosion and infection. Women who experience transvaginal mesh failure may need to have numerous corrective surgeries, IV therapy, blood transfusions and drainage of hematomas or abscesses." The US Drug Watchdog is has expanded their national initiative designed to help women recipients of transvaginal mesh, tape, or sling, who are now severely injured by these types of medical products-because the need is so great. For more information women, who are victims of a transvaginal mesh failure are urged to contact the US Drug Watchdog anytime at 866-714-6466. http://USDrugWatchdog.Com

The US Drug Watchdog says, "We are having a huge problem trying to help victims get information out of the surgeon, who initially installed the transvaginal mesh, tape, or sling. Ignoring these women victims will not make vaginal erosion go away. If the US FDA, the doctors, and these device makers do not get real attentive to these victims immediately-we will make this mess so expensive-the phrase costs beyond comprehension will have to be redefined." http://USDrugWatchdog.Com

The US Drug Watchdog is indicating symptoms of a transvaginal mesh, tape, or sling implant failure may include:

  • Pain during sexual intercourse caused by erosion.
  • Mesh erosion through the vagina (the mesh is actually protruding out of the vaginal wall)
  • Vaginal Bleeding
  • Non-Stop Vaginal Infection
  • Urinary problems-Non Stop UTI's
  • Organ perforation
  • Hardening of the vaginal mesh
  • Injury to nearby organs
  • Severe Pelvic Pain

The US Drug Watchdog says, "One of the biggest problems we have with respect to our failed medical device or recalled drug initiative work is the average US consumer never hears about a drug recall or failures involving medical devices like a transvaginal mesh failure. If you have a friend, or loved one who is a recipient of a transvaginal mesh product that has already failed or is showing symptoms of a failure, please have them call us at 866-714-6466. We want to make certain all women, who are transvaginal mesh failure victims get to the best possible attorneys, to ensure they get the best possible compensation for their ordeal, and we will do our absolute best to make certain all of the attorneys are women." http://USDrugWatchdog.Com

U.S. District Court for the Southern District of West Virginia Multidistrict litigation (MDL) consolidates all similar cases into one courtroom and will include the Defendants:
C.R. Bard, Inc., (MDL No. 2187);
American Medical Systems Inc., MDL No. 2325);
Boston Scientific Corp., (MDL No. 2326); and Johnson & Johnson's Ethicon, Inc. (MDL No. 2327)


Contact

  • M Thomas Martin
    Americas Watchdog
    866-714-6466
    Email

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