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US Drug Watchdog Launches An Aggressive National Initiative On The Transvaginal Mesh Disaster For Women And Offers The Names and Contacts Of The Best Women Attorneys

June 12, 2012

The US Drug Watchdog is launching an aggressive initiative designed to help women recipients of a transvaginal mesh, who are now severely damaged by this type of product. Transvaginal mesh was designed for women, who were suffering from pelvic organ prolapse and stress urinary incontinence. According to the US FDA the procedure to install a transvaginal was supposed to be minimally-invasive. The US Drug Watchdog now says, “The Transvaginal Mesh Disaster is the worst mess we have ever seen for women. The FDA is now saying transvaginal mesh failures is causing complications in patients such as erosion and infection. Patients who experience transvaginal mesh failure have needed corrective surgery, IV therapy, blood transfusions and drainage of hematomas or abscesses.” The US Drug Watchdog is offering to help any victim of the transvaginal mesh disaster get to the best possible attorneys, and the group is promising the attorneys will all be women. For more information victims of the Transvaginal Mesh Disaster are urged to contact the US Drug Watchdog anytime at 866-714-6466, or contact the group via their web site at http://USDrugWatchdog.Com

(PRWEB) June 12, 2012

The US Drug Watchdog says, “We may have thousands, or even tens of thousands of women in the United States, who are in unspeakable pain, or they have been damaged beyond comprehension, because they got sold a bill of goods, on what we are calling the Transvaginal Mesh Disaster.” Transvaginal mesh failure occurs when the mesh fails to bind to the pelvic tissues. As a consequence of this, the body rejects the mesh that has been sewn into it. As a result, the transvagina mesh may start to poke its way through the vaginal wall and protrude out of the vaginal tissue. This complication is more commonly referred to as “erosion.” Erosion may result in extreme pain, infection, bleeding or vaginal discharge. The US Drug Watchdog has begun a very aggressive initiative designed to assist women in the United States, in what they are referring to as the Transvaginal Mesh Disaster. The group is urging any woman, who has had the transvaginal mesh surgical procedure done, and now has developed severe complications to call them anytime at 866-714-6466. As part of its initiative the US Drug Watchdog is offering to send all US women, who are victims of this Transvaginal Mesh Disaster to national caliber attorneys-who are all women. http://USDrugWatchdog.Com

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 the Transvaginal Mesh Disaster. If you have a friend, or loved one who is a recipient of a Transvaginal Mesh 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 these Transvaginal Mesh Disaster 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 Ethicon, Inc. (MDL No. 2327)

For the original version on PRWeb visit: http://www.prweb.com/releases/prweb2012/6/prweb9595991.htm


Source: prweb



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