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  • File A Talcum Powder Lawsuit: Talcum Powder Ovarian Cancer Lawsuits Talcum Powder Fallopian Tube Cancer Lawsuits Baby  Powder Ovarian Cancer Lawsuits Filed If you or a loved one used talcum powder products and were diagnosed with ovarian cancer, or fallopian tube can...

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Drug Class Actions

  • Taxotere Lawyers for Permanent Hair Loss: Taxotere Baldness Lawyers For  Permanent Hair Loss Lawsuits Have you received Taxotere for breast cancer? Taxotere can result in hair loss or baldness  that is permanent. Taxotere  is a chemotherapy drug used for the treatment of breas...

Medical Device Lawsuits

  • Get A Hernia Mesh Lawyer | Hernia Mesh Lawsuits Filed: The hernia mesh lawyers of Class Action Lawyer Network are filing hernia mesh lawsuits for victims of a failed hernia mesh. We have Ethicon, Bard and Cook hernia mesh lawyers. Hernia Mesh Lawsuits Filed  For: Ethicon: Physiomesh Pro...

Posts Tagged ‘st. augustine’

Risperdal Lawyers | Enlarged Breasts in Boys Lawyers

Written by lisaspitzer on . Posted in Class MDL Class Action News

Our Risperdal lawyers are accepting cases for unusual breast development in males. Risperdal  $70M Verdict In Philadelphia  Risperdal  Trial Johnson & Johnson was hit with a $70 million verdict on Friday when a  Philadelphia jury found that the antipsychotic drug Risperdal had caused an adolescent boy to grow female breasts. Risperdal and Enlarged Breasts In Young  Males Risperdal   has been linked to enlarged breasts in your males. This is  a condition called gynecomastia. he Growth of male breasts can cause severe emotional distress.  Surgery may be required to correct the condition.  Risperdal may increase levels of prolactin, a hormone which stimulates breast development in women. Young boys who have taken prolactin and are displaying increased levels of this hormone may develop male breasts or gynecomastia. Can I Join The Risperdal Gynecomastia Lawsuits? If you  are a male and have  enlarged female breast call no to see if you qualify to join others in a Risperdal lawsuit. Risperdal is the  brand name for the drug called Risperidone. This is approved to treat schizophrenia and bipolar disorders. Risperdal  but has resulted in gynecomastia. Gynecomastia, the development of real female breasts.  It is real breast tissue growth caused by an increase in the hormone prolactin. If you have enlarged breasts with; Pain, Swelling, Tenderness and Nipple discharge and may need surgery  to remove excess breast tissue you may be able to join the Risperdal class action lawsuits. Get A Risperdal Lawyer Lawsuits are being filed against  Johnson & Johnson through its subsidiary Janssen Pharmaceuticals, for  failing to properly inform doctors and patients about the effects of Risperdal.  

Talcum Powder Ovarian Cancer Lawsuits

Written by lisaspitzer on . Posted in Class Action Articles, Talcum Powder cancer lawyers

Lawyers Filing Ovarian Cancer Lawsuits For Baby Powder

Talcum Powder Ovarian Cancer Lawsuits Do You Want To File A Baby Powder Cancer Lawsuit?

Studies show that talcum-based powder can  cause ovarian cancer in women who have used it for genital/perineal hygiene. Studies dating back to 1982 have consistently linked prolonged talc-based baby and body powder usage with ovarian cancer.  The talc particles moves  through the female reproductive system and settles in the ovaries. These particles may remain in the ovaries for many years, creating inflammation resulting in the development and proliferation of cancer cells. Studies HAVE Linked  Ovarian Cancer to Talc-Based Baby/Body Powder The pathology reports and tissue samples that were used to diagnose the ovarian cancer can now be examined to determine whether your ovarian tissues contain talc particles.  Talc particles can be found in the pelvic lymph nodes, ovaries, and fallopian tubes and take many years to disintegrate and exit the body. The talcum powder cancer lawyers at Class Action Lawyer Network are speaking to women about  talc having  caused your ovarian cancer.

Speak To A Talcum Powder Lawyer

If you have been  diagnosed with ovarian cancer after long term  use of talcum-based products, such as Johnson & Johnson Baby Powder, Shower to Shower, and others  we want to talk to you regarding  filing a talcum powder cancer lawsuit.

Was There Sufficient Warning For Boston Transvaginal Mesh Victims?

Written by lisaspitzer on . Posted in Medical Device Lawsuits, Transvaginal mesh

Did The Manufacturers Of The Transvaginal Mesh And Bladder Sling Give Sufficient Warning?

Boston Vaginal Mesh Lawyers say no in the thousands of transvaginal mesh and bladder sling claims that have been filed in the Pelvic Mesh Repair Lawsuits MDL'Ls.

According to transvaginal mesh lawyers accross the country who are filing vaginal mesh and bladder sling lawsuits the warning was insufficient. For a warning to be sufficient, a transvaginal mesh warning  should appropriately signal danger while simultaneously providing the information in order to use the product appropriately.  A  pharmaceutical or medical device  manufacturer doesn’t necessarily have to discuss matters that are basic medical knowledge.  They are not in a position to control the individual practices  of doctors in every single medical community. 

 Will The Device  Warnings The Transvaginal meshmanufacturers provided  to the doctor relieve them of their duty to warn the patient.

What are some ways that warnings can become inadequate?  Some variables that courts will consider include:  If they are overly broad or too generic, contradictory statements made in the inserts, actions by the sales representatives, and presenting the warning in a way that makes it unlikely to be read.  Remember, every case is different.  In some cases, a doctor might not even bother to read the warnings.  In other cases, the possibility of an adverse reaction is too small to even impact the doctor’s decision.  There have even been cases where a doctor has stated that even if he were given new information, he would have still followed through with his initial decision.

What other possible legal theories being explored?  If a company supplies product related information to the public that amounts to an express warranty, they can be held liable for breach of warranty if the plaintiff can successfully prove that the information was false.

We will be watching the pelvic mesh repair proceedings and waiting to see how they play out.

To file a Transvagina, mesh lawsuit for a Prolene mesh surgicall implanted in: D.C., Daytona, Fort Myers, Ft Lauderdale,  Gainesville,  Jacksonville,  Keys,  Lakeland, Miami, Ocala, Orlando, Panama City, Pensacola, Sarasota, St. Augustine,  Boston, Springfield,  Worcester, Ann Arbor, Detroit,  Grand Rapids, Jackson, Lansing, Minneapolis,  St Paul, Charlotte. Fayetteville,  Greensboro,  Raleigh, Wilmington, Winston Salem, Fargo, Providence,  Charleston, Columbia,  Florence, Greenville, Seattle, Tacoma, Charleston,  Wisconsin, Milwaukee,  Cheyenne,  Casper,  Laramie,  Gillette, Milwaukee, Montana, Billings, Springfield, Detroit, Grand Rapids, Omaha ,Manchester, Albuquerque, Charlotte, Raleigh, Greensboro, Winston-Salem, Durham,  Fayetteville,  Wilmington, Providence, Charleston  Seattle, Milwaukee, Madison,  Green Bay, Casper or Laramie call Class Action Lawyer Network transvaginal mesh attorneys today.

Gynemesh Transvaginal Mesh Lawyers

Written by lisaspitzer on . Posted in Class MDL Class Action News

Gynemesh Class Action Lawyers are filing lawsuits against the manufacturers of the Gynemesh transvsagina mesh Implant in 3, 4, 5 and 6 year product liability statute states.

Our Gynemesh Class Action  Lawyers Are Accepting Transvaginal mesh Lawsuits

For Gynemesh Vaginal Mesh Surgically Implanted In The Following 3, 4, 5 and 6 year product liability statute states.

 D.C, Florida, Maine, Massachusetts, Michigan, Minnesota, Montana, Nebraska,  New Hampshire, New Mexico,  North Carolina,  Rhode Island, Rhode Island, South Carolina, Washington, Wisconsin, and Wyoming.

   Ethicon Gynecare Prolift Pelvic Mesh Lawsuits For Ethicon Gynecare Gynemesh

    Ethicon Gynecare Prosima Pelvic Mesh
    Ethicon Gynecare Gynemesh
    Ethicon Prolene Mesh
    Ethicon Gynecare TVT Sling

An Ethicon Gynemesh  vaginal mesh or bladder sling lawsuits are being filed  for women who have experienced complications.

Gynemesh Complications Include

  •     Infection
  •     Erosion of the Mesh
  •     Urinary Problems
  •     Digestive problems
  •     Pelvic Pain
  •     Re Prolapse
  •     Injury to Nearby Organs
  •     Difficulty during intimacy

The FDA has received reports of problems with Ethicon Gynemesh vaginal mesh implants

Overview Of  Ethicon Gynecare Gynemesh

Gynecare Gynemesh was first introduced in October 2002. Gynemesh is also called the Gynecare GynemeshPS, nonabsorbable Prolene Soft Mesh, for vaginal wall prolapse surgical treatment.

What Is Ethicon Gynemesh?

Ethicon Gynemesh is porous, which allows surrounding tissues to grow into and incorporate the material as part of the body, which can create severe complications. If you are a victim of a faulty Gynemesh Vaginal Mesh

Speak To A Gynemesh Lawsuit Attorney Today

Coopvision Avaira Toric Contact Lense Lawyers, Lawsuits on the rise

Written by Class Action Lawyer on . Posted in Product Recall News

Class Action lawyer Network announces a new helpline for Avaira Toric Contact Lense Complications. CooperVision is  recalling  the Avaira Toric brand contact lenses because they were manufactured and distributed with unintended silicone residue. This harmful adulteration has led to serious  eye complications including eye pain, blurring, haziness of vision, and even total vision loss. There are increasing reports of serious eye injuries including corneal ulcers, corneal lesions, corneal abrasions, corneal edema, corneal erosion, and keratitis. Other complaints include blurry or hazy vision often described as a white or opaque film over the eye, severe eye pain, burning, redness, dryness, light sensitivity, and vision impairment. While some users may suffer only temporary side effects, others may require urgent medical care or experience permanent vision loss.The CooperVision Avaira Toric contact lens recall has been classified by the U.S. Food & Drug Administration (FDA) as a Class I Recall, which means that using the product can potentially lead to severe side effects and complications. There can be sever damage to the eyes. If you or a loved one is useing the Coopervision Avaira Contact lenses and showing side effects see you eye doctor immediately and call Class Action Lawyer network for an immediate case review.

Anyone who used Avaira Toric contact lenses or Avaira Sphere contact lenses who has suffered adverse side effects or whose contact lenses are affected by the Avaira contact lens recall should contact a medical device or contact lens Class Action Lawyer Network attorney who will evaluate your case. It is also very important to keep the contact lenses and all original packaging because this is evidence that will be important in a lawsuit.

Call Class Action lawyer Network for a free CooperVision Avaira Toric Contact Lens Recall Lawsuit Evaluation: If you or a loved one has been injured by CooperVision Avaira Toric contact lense recall contact  the Class Action lawyer Network. You may be entitled to compensation by filing a lawsuit against CooperVision.

 

 

Anyone who used Avaira Toric contact lenses or Avaira Sphere contact lenses who has suffered adverse side effects or whose contact lenses are affected by the Avaira contact lens recall should contact a medical device or contact lens Class Action Lawyer Network attorney who will evaluate your case. It is also very important to keep the contact lenses and all original packaging because this is evidence that will be important in a lawsuit.

Call Class Action lawyer Network for a free CooperVision Avaira Toric Contact Lens Recall Lawsuit Evaluation: If you or a loved one has been injured by CooperVision Avaira Toric contact lense recall contact  the Class Action lawyer Network. You may be entitled to compensation by filing a lawsuit against CooperVision.