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Nationwide Testosterone Lawyers For Heart Attack and Stroke Victims


Nationwide Testosterone Lawsuit Attorney Network


Get A  Testosterone Lawsuit  Lawyer  Handling Testosterone Heart Attack and  Stroke Lawsuits

If you or a loved one suffered from a heart attack or stroke while using AndroGel you may be entitled to damages. We provide free no-obligation Atlanta testosterone lawsuit case review. We do not charge attorney fees unless you receive compensation and you are under no obligation after your initial consultation.

Testosterone Therapy May Raise Heart Attack Risks

Researchers say risk of heart attack doubles after treatment starts for men under 65 with heart problems and all men over 65.

Nationwide  AndroGel  Lawsuit Attorneys
Testosterone Stroke and Heart Attack

AndroGel® (testosterone gel)  is a daily testosterone replacement therapy  that can help bring T levels back to normal with daily use.

FDA Is  Investigating Potential  Heart Attacks And  Strokes From Testosterone Products

On Jan. 31, 2014, the  FDA announced  it would be investigating the risk of heart attacks, strokes and possible  deaths in men using  testosterone products. The FDA made this announcement after reviewing the study conducted at the National Cancer Institute, as well as the study published in JAMA. The FDA recommended the health care practitioners should  consider the benefits of testosterone treatment and potential the  risks.

If you or a loved one has had a stroke or heart attack after using testosterone therapy call now and get connected to one of our experienced testerone lawyers

 

 

 

 

 

Cystocele and Rectocele Mesh Repair, FDA Warnings

Risks with Cystocele and Rectocele Mesh Repair, FDA Warnings, Vaginal mesh lawyers

In July 2011, the FDA released a safety communication warning healthcare providers of the serious risks associated with surgical mesh used to repair pelvic organ prolapse (POP) and stress urinary incontinence (SUI). Specifically, the FDA stated that complications were not rare, and that surgery with the mesh may be no better than traditional surgery options that don’t use mesh.

Public Citizen and Vaginal mesh

In October 25, 2011, a consumer advocacy group called Public Citizen submitted an appeal to the FDA that all non-absorbable vaginal mesh be recalled. They stressed that there is a need for these non-absorbable vaginal meshes to be removed from the market since it’s benefits over other non-mesh procedures used to repair POP and SUI were unseen, and patients who received them developed fatal reactions.  The group also recommends that all non-absorbable vaginal mesh be tested appropriately for safety and effectiveness before the FDA approves its availability in the market.

FDA 510 (K) Process

Manufacturers needed  only to show they were similar to devices already on the market to gain approval through the FDA’s 510(k) approval process. The remaining eight recalled devices didn’t have to go through any kind of FDA review. Of the 113 recalls, 35 were for cardiovascular devices, including automated external defibrillators, or AEDs, and only 12 of them had been required to undergo patient testing.

POP repair surgeries may include cystocele and rectocele.                                                                                                      Unfortunately, complications have been found with both.
Types of POP Repair Include Cystocele and Rectocele.The sling procedure, or suburethral sling procedure, refers to a particular kind of surgery using ancillary material to aid in closure of the urethral sphincter function of the bladder. It is performed as a treatment of severe urinary incontinence. The sling procedure, also known as the suburethral fascial sling or the pubovaginal sling, has many forms due to advances in the types of material used for the sling. Some popular types of sling material are Teflon (polytetrafluoroethylene), Gore-Tex ® , and rectus fascia (fibrous tissue of the rectum).

Cystocele and  rectocele repair

  •     Cystocele—bladder prolapse
  •     Rectocele—rectal prolapse (end of the large intestine, or rectum)
  •     Uterine prolapse
  •     Vaginal prolapse
  •     Enterocele—herniated small bowel

Mesh was initially incorporated into POP surgical repair because it offered more support to the affected organ and helped shore up surrounding muscles and tissues. Since the risk for recurrence of prolapse is high in women who have cystocele surgery and rectocele surgery, the hope was that surgical mesh would help sustain the repair. The FDA received many reports, however, or cystocele mesh complications and rectocele mesh complications.

Mesh complications

  • erosion of mesh
  • serious infection
  • recurrence of pop / sui
  • perforation
  • pain
  • corrective surgeries
  • injury to other organs
  • vaginal scarring
  • urinary problems
  • hardening of mesh

Cystocele Mesh Complications and Rectocele Mesh Complications

During cystocele surgery, transvaginal mesh is inserted through the vagina to help act as a barrier and to hold the bladder in place. The mesh is also intended to help stop related problems like incontinence.

A rectocele occurs when the thin wall of tissue separating the rectum from the vagina weakens, allowing the front of the rectum to bulge into the vagina. During rectocele surgery, excess stretched tissue is removed through the vagina, and a mesh patch may be used to support and strengthen the wall. (Surgery may also proceed from the abdomen, anus, or perineum.)

Though surgical mesh does seem to provide better support for pelvic organs, cystocele mesh complications and rectocele mesh complications made the improvement a moot point. The FDA, in its 2011 warning, mentioned that it had received nearly 3,000 reports of vaginal mesh complications between 2008 and 2010, with the most common being mesh erosion through the vagina. Mesh erosion can require multiple surgeries to repair and may be extremely debilitating.

Other cystocele mesh complications and rectocele mesh complications included pain, infection, bleeding, pain during sex, organ perforation, urinary problems, recurrent prolapse, vaginal scarring/shrinkage, and neuro-muscular problems. Many required additional surgical treatment and hospitalization.
Cystocele Surgery and Rectocele Surgery

Cystocele, urethrocele, enterocele, and rectocele are particularly likely to occur together. Urethrocele is virtually always accompanied by cystocele (cystourethrocele). Cystocele and cystourethrocele commonly develop when the pubocervical vesical fascia is weakened. Enterocele usually occurs after a hysterectomy. Weakness in the pubocervical fascia and rectovaginal fascia allows the apex of the vagina, which contains the peritoneum and small bowel, to descend. Rectocele results from disruption of the levator ani muscles.

Severity of these disorders can be graded based on level of protrusion:

  •     1st degree: To the upper vagina
  •     2nd degree: To the introitus
  •     3rd degree: External to the introitus

If you have been injured due to a vaginal mesh from any of the manufactuirers listed below  contact Vaginal mesh Helpline 1 877 522-2123

Manufacturers

Johnson & Johnson

  •     Ethicon TVT
  •     Gynecare Prolift
  •     Gynecare Prosima
  •     Gynecare TVT
  •     Gynemesh PS

C.R. Bard

  •     Avaulta PlusT BioSynthetic Support
  •     Avaulta SoloT Synthetic Support
  •     Faslata Allograft
  •     PelvitexT Polypropylene Mesh
  •     Pelvicol Tissue
  •     PelviSoft Biomesh

Boston Scientific

  •     AdvantageT Sling System
  •     Prefyx Mid UT Mesh Sling System
  •     Prefyx PPST System
  •     Obtryx Curved Single
  •     ObtryxMesh Sling
  •     Arise
  •     Pinnacle
  •     Solyx
  •     Lynx

American Medical Systems

  •     SPARC
  •     BioArc
  •     MiniArc
  •     Apogee
  •     Elevate
  •     Monarc
  •     In-Fast
  •     Perigree

vaginalmeshhelpline.com