Posts Tagged ‘Florida’

Vaginal Mesh Lawyers Filing Nationwide Vaginal Mesh Lawsuits

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh helpline, vaginal mesh lawyers are filing lawsuits for women injured by the vaginal mesh. If you have been rejected due to the statute of limitations or other criteria call the Vaginal Mesh Helpline to speak to one of our experienced mesh lawyers today.

The vaginal mesh lawsuit bellwether trials have begun and the mesh lawsuits are heating up. You must file your mesh lawsuit immediately.

What are the Transvaginal Mesh Complications ?

  • Erosion of vaginal tissue can result from a vaginal mesh
  • Hardening of the vaginal mesh
  • Infection is a serious mesh-patch complication
  • Pain and discomfort
  • Perforations of the bowel, bladder or blood vessels
  • Recurrence of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI)
  • Urinary problems and more severe incontinence
  • Painful sexual intercourse
  • Potential injury to the partner
  • Feeling the mesh or pieces of substance in the vaginal canal
  • Vaginal mesh erosion
  • Increased incontinence
  • Lower back pain
  • Abdominal pain
  • Gastrointesitnal discomfort
  • Bladder and or bowel incontinence
  • Difficulty voiding and the need for self catherizations
  • Vaginal scarring

Vaginal Mesh Lawsuits Are  Against These Manufacturers

  • C.R. Bard’s Avaulta
  • Ethicon’s Gynecare
  • American Medical Systems’ products:
  • AMS Apogee
  • AMS BioArc
  • AMS Elvate
  • In-Fast Unltra
  • MiniArc
  • Monarc
  • AMS Perigee
  • SPARC
  • Straight-In mesh
  • Boston Scientific Scimmed’s Pinnacle pelvic mesh
  • Covidien
  • Sofradim
  • Caldera
  • Mentor Corporation

To file a vaginal mesh lawsuit call us today.

 

Yaz Birth Control Pills Lawyers, New April 2012 Warning Date, Yaz Lawyers Filing Yaz Lawsuits

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh Information

The VaginaL Mesh Helpline is keeping women updated on all dangerous drugs and devices harming women. Many women were injured by Yaz  birth control pills and thought that they were out of luck in filing a Yaz lawsuit. Yaz complications  include: Blood clots, stroke, pulmonary embolism, deep vein thrombosis and in some instances death. Many women with complications and families that have lost loved ones due to Yaz felt they could not file a lawsuit. But, new warnings issued in April pf 2012 has opened doors for an influx of Yaz lawsuits. We do not want you to be left out.

The FDA Ordered  Warning Label Changes For  Yaz Blood Clots

The FDA announced it was requiring a label change for  Yaz

On April 10, 2012, the FDA announced it was requiring a label change for Yaz which contains Drospirenone. This warning   announced that Yaz may be associated with a higher risk for blood clots due to Drospirenone. This warning date may mean you now have a Yaz lawsuit even though you may have been turned away before.

Yaz  Lawsuit Complications

  • Blood Clot
  • Stroke
  • Pulmonary embolism
  • Deep Vein Thrombosis

Blood clots from Yaz may be linked to an increased risk of stroke, deep vein thrombosis and pulmonary embolism injuries to the lungs.

A federal Multi-District Litigation court in Illinois set up to handle lawsuits filed over alleged Yaz side effects has reported more than 10,000 cases filed. The formal case is known as Yasmin and Yaz (Drospirenone) Marketing, Sales Practices and Products Liability Litigation (MDL No. 2100).

Yaz lawsuit lawyers are accepting lawsuits from women who have have suffered these  side effects after taking Yaz. Yaz blood clots have caused premature death in young women. This is another medical product that targets women. Women must stand up and demand justice.

Vaginal Mesh Lawsuit, Urgent Statute Of Limitations Notice

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

After July of this year many vaginal lawyers will no longer be accepting vaginal mesh lawsuit cases for states with 2 year statute of limitations. The number of lawyers still accepting cases for states with 1 yr statutes is minimal. States with 1 year statutes include: Tennessee, Louisiana,  and Kentucky. At the end of July women in the states with 2 year statutes may have a difficult time finding lawyers to accept their vaginal mesh lawsuits as well.

After July there will be a number of states left with 4 year and 6 year statutes of limitations. But, even if your vaginal mesh was implanted in one of these “lucky” states you should not procrastinate getting your lawsuit filed. If you have had your mesh implanted in a state that is not on the list below you will need to find a very creative and shrewd lawyer or law firm that will accept your case.

The following states have 4 or 6 year statutes:

Arkansas, Washington D.C, Florida, Maine, Massachusetts, Michigan, Minnesota, Mississippi, Montana, New York, North Carolina, Rhode Island, South Carolina and South Dakota, Utah, Washington, Wisconsin, Wyoming are all 4 to 6 year states.

To find out more about the vaginal mesh lawsuit updates check back on this site frequently. We are always posting the latest information. Do not despair. We may be able to locate a lawyer who will accept your case even if  your mesh was implanted in a one year or two year statute state.

We are extremely concerned about the women who may been left out and urge you contact us right away.

First Vaginal Mesh Trial, Vaginal Mesh Lawsuit Victory, Ladies We Are Starting To Win The Battle

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh Information

A $3.35 Million partial verdict was handed down in first vaginal mesh trial.  This is good news for women who have suffered from a vaginal mesh implant. The Vaginal Mesh helpline hears horror stories every day and we applaud our first victory as the pathway to help other women whose lives have been ruined by the Prolene mesh. Vaginal mesh lawyers have been watching and agee this is good news for future trials.

The jury declared that  Johnson & Johnson should pay a South Dakota woman $3.35 million for failing to adequately warn her doctor of the potential dangers of a vaginal mesh implant made by the company’s Ethicon Inc subsidiary, and for misrepresenting the product in brochures.  It is the first verdict among some 1,800 vaginal mesh cases pending in New Jersey against Ethicon and J&J, and can potentially  set the way for  thousands of lawsuits and trial outcomes against  manufacturers of vaginal mesh implants.

February 25, 2013

ATLANTIC CITY, N.J. — A New Jersey state court jury has handed down a partial verdict of $3.35 million against Johnson & Johnson (NYSE: JNJ) and its subsidiary, Ethicon Inc., at the end of the first pelvic mesh case to go to trial, Harris Martin Publishing is reporting.

In a Feb. 25 verdict, the jury found by a 7-2 vote that the manufacturers failed to adequately warn plaintiff Linda Gross’s implanting surgeon of the risks associated with the pelvic mesh and, additionally, that the device was the proximate cause of injury. By a 7-2 vote, the jury  was on our side.

We have been listening to 1000′s of women over months calling from all states and of all ages. Their marriages have been destroyed and they are suffering. The youngest was 33 and the oldest 86. We have heard from women, mothers, daughters, grandchildren , and friends for friends that are so debilitated they cannot come out of bed to call on their own. They need help from doctors and cannot afford surgeries to “Get the damn thing out”.

We demand justice on behalf of these women and are happy to see it is starting to happen. Can money change this? Atleast is will pay for medical care and send a message that manufacturers that use women to gain profits must end.

Stryker Hip Replacement Effects Women More, Stryker Hip Replacement Lawyers For Women

Written by Vaginal Mesh Helpline on . Posted in Stryker Hip Replacment lawyer for Women, Vaginal Mesh News

The Vaginal Mesh Helpline continues it it’s mission to inform about all dangerous drugs and devices harming women. It appears that even the recent hip replacement recalls effect women more then men. When will women stop being the target of these manufacturers? The vaginal mesh has caused severe injury. Just today we received a call from a woman about her mother of 76 who must wear a colostomy bag after mesh removal. And now the FDA reports that these metal on metal and metal component hip implants  put women at a higher risk. Both the Stryker Rejuvinate and ABG II are  dangerous surgical implants that have a greater failure rate and complications for women.

Many articles and reports have been released that discuss hip replacements having a greater failure rate in women.

Hip replacements like Stryker Rejuvinate and ABG II are slightly more likely to fail in women than in men, according to research published Monday in JAMA Internal Medicine.  The research was financed by the Food and Drug Administration. Another report discusses hip resurfacing and states a drawback for women because of the bone weakening that accompanies menopause. Meanwhile, even advocates of resurfacing acknowledge that they have yet to agree on how best to screen women for the procedure.

“We were surprised by the results, as studies suggest that larger heads should have  lower wear and a lower risk of dislocation. However, we have seen an increase in revisions for pain and loosening, particularly in women,” says Alison Smith, a study author and statistician at the University of Bristol in the U.K. Depending on patient age and implant head size, the revision rate for all-metal hips is three to four times higher in women and two to three times higher in men compared with other implants.

The FDA Reports Women At a Higher Risk For Failure

The Food and Drug Administration, along with its safety communication, has included a list of risk factors that can increase a patient’s chances of suffering from metal on metal hip implant complications. Patients who are overweight, female, or physically active are more likely to suffer complications related to these hip replacement systems, and patients who have a sensitivity to certain metals, have kidney failure, have a suppressed immune system, or take corticosteroids are also more at risk.

It seems women are always the victims for these manufacturers that choose profits over warnings.

Hip Replacement Failure More Likely In Women, Study Says Studies on Google News Today

Hip replacements are more likely to fail in women than in men, but the overall risk of implant failure is low–according to a study published in the Journal of the American Medical Association, JAMA, and that was funded by the U.S. Food and Drug Administration.

Women account for the majority of the more than 400,000 patients who undergo either full or partial hip replacements in the U.S. each year.

“This is the first step in what has to be a much longer-term research strategy to figure out why women have worse experiences,” said Diana Zuckerman, president of the nonprofit National Research Center for Women & Families.

It appears the smaller frame and difference in the curve of the hip and pelvic region accounts for this. Anatomy appears to play a role.  Women tend to have smaller joints and bones than men, and so they tend to need smaller artificial hips. Devices with smaller femoral heads  the ball-shaped part of the ball-and-socket joint in an artificial hip are more likely to dislocate and require a surgical repair.

I wonder why there cannot be two types of replacements, one for women and one for men. But, since they are all being recalled it would just mean more injured women. I am sure there would be extensive marketing to hook women in explaining how their lives would remain active and have a better quality. If you or a wife, mother, girlfriend or female loved one has been injured by these hip implants contact us and we will direct you to a Stryker Hip Replacement lawyer.

 

 

 

 

Avautla Mesh Lawsuit Trials Begin

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

The first transvaginal mesh trial against C.R. Bard and its Avaulta Transvaginal Mesh product was set for February 5, 2013. The push is on to get Bard’s device and other vaginal mesh products off the market before they can do further harm. The Vaginal Mesh Helpline I watching and waiting with hopes of justice for the many women suffering from:

 

  • Erosion of the mesh through the vaginal  wall
  • Relentless  pain
  • Exposure or extrusion of mesh
  • Lower back pain and razor blade pain
  • Painful sexual intercourse
  • Perforation or puncture of the bladder, intestines and bowels, as well as blood vessels around the vaginal wall
  • Recurrent Pelvic Organ Prolapse (POP)
  • Recurrent Stress Urinary Incontinence (SUI)
  • Urinary problems
  • Vaginal bleeding
  • Constant  discharge and infections
  • Ruined lives and marriages
  • Vaginal scarring and shortening

The First Stage of the Avaulta Mesh Lawsuit Trials

Dr Uwe Klinge, a world-renowned expert on the biocompatibility of surgical mesh, explained to a jury during a talk he delivered in 2005 to J&J. Dr Klinge told the manufacturer’s Ethicon unit that surgical mesh could only be safe for patients when used in the pelvis if it was very lightweight and had pores that were at least 1 millimeter in all directions. But Ethicon chose to ignore his advice. They marketed the Prolift vaginal mesh kit made with mesh that was larger and heavier than Dr. Klinge said it needed to be for patients’ safety.

We hope for a positive outcome for thousands of women harmed by failed mesh products. it is not too late for you if you have a Bard vaginal mesh. The outcome of this trial is just the beginning. File your mesh lawsuit today.

,

 

 

 

 

Vaginal Mesh Lawsuits Updates, New News From Vaginal Mesh Lawyers

Written by Vaginal Mesh Helpline on . Posted in Medical News and Your Vaginal Mesh, Vaginal Mesh News

Vaginal Mesh Helpline is keeping women informed with a mesh update on the all the new  vaginal mesh lawsuits. All vaginal mesh lawyers suggest filing your mesh lawsuit  right away. We do not want any women to be left out.

A 47-year-old former nurse, Gross testified that Ethicon’s Prolift vaginal mesh implant has rendered her unable to work, have sex with her husband, or sit comfortably for more than 20 minutes. (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey.) Gross also said that, as a result of the Prolift mesh, she takes up to 20 medications a day and has undergone more than 400 medical encounters, including physical therapy sessions, doctor visits, and many surgeries.

The Charleston woman claims that she suffered serious complications after AMS surgery, when she was implanted with the Elevate transvaginal mesh back in January 2011. The lawsuit alleges that she suffered substantial physical pain and suffering, emotional distress, and economic loss due to medical expenses. These damages, according to the suit, were the direct result of the AMS transvaginal mesh manufacturer’s negligent and wrongful actions. Further, the defendants, AMS, allegedly knew about the risks involved with its transvaginal mesh product but failed to warn the plaintiff.

A Georgia women’s  doctor suggested the mesh when she mentioned that she had bladder leakage when she laughed or coughed. Shortly after the surgery, it felt like razors were slicing her organs and a sharp edge of the mesh cut her boyfriend during sex, she said. Even though she eventually had it removed, the 55-year-old west Georgia woman still has pain she believes is caused by the mesh.

According to court documents, on January 7th, 2013 a Minnesota woman filed a lawsuit in Minnesota District Court (case no. 0:2013cv00060) alleging she suffered serious complications from her Transvaginal Mesh. Transvaginal surgical mesh is used to treat pelvic organ prolapse (POP) and Stress Urinary Incontinence (SUI). Defendant is Boston Scientific and in the lawsuit, plaintiff claims that after surgical implantation with defendant’s Lynx sling she suffered complications.

Vaginal mesh Bell Weather Case Updates

The  first bellwether trials in the Transvaginal Mesh MDLs have been scheduled to start in December 2013. Defendants in the first three bellwether trials are American Medical Systems (AMS), Boston Scientific and Ethicon. (American Medical Systems is referred to as MDL 2325).

 

FDA Adverse Incident Reports On the Vaginal Mesh

The FDA received more than 1,000 complaints associated with trans vaginal mesh between 2005 and 2007. That number almost tripled between 2008 and 2010.

The Vaginal Mesh stories of suffering go on and on with more women filing lawsuits every day. The Vaginal Mesh Helpline has a mission, We must locate all women suffering from these Prolene mesh implants after 2001 and get them to a mesh lawyer to file their transvaginal mesh lawsuit today.

Be aware that all these devices have fancy names but they are all mesh. If you have a Prolene product implanted in you for prolapse or urinary incontinence call the Vaginal Mesh Helpline today. It is most likely one of these mesh devices that women are  filing vaginal mesh lawsuits for nationwide. Be aware you must move quickly. Statute of limitations for states are running close. If you have a current mesh lawyer call today and get and update. Find out who has your vaginal mesh file. Many lawyers may have referred your case out. Find out if your lawsuit was filed. Since the mesh is now a consolidated MDL it is extremely easy for lawyers to file the lawsuits. The Bellwether trials will begin soon…Do not be left out. Stay on top of things. if you need help or have questions call the Vaginal Mesh Helpline today. If you have received a rejection letter from a law firm do not give up hope. call us about your vaginal mesh lawsuit today. We will make every attempt to locate a vaginal mesh lawyer for you to take your case. But, these must be mesh implanted after 2001, closer to 2002.

 

Mesh Lawyers are Filing Nationwide Mesh Lawsuits, The Mesh Trials Have Begun

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

The Vaginal Mesh Helpline announces the mesh trials have begun. Mesh lawyers are filing mesh lawsuits in droves. The quantity is increasing daily. Soon we will see justice. We all know the monetary compensation will never be enough for the agonies I have heard from our callers but, it is a first step. The FDA has not removed the mesh from the market even to this date. We must send a message to these mesh manufacturers.

We will keep you posted on the  mesh lawsuit  with mesh trial updates

Many  makers of Mesh Implants have faced their first jury trials and the outcome was seven figure jury awards for women victims these cases. Mesh implant manufacturers face a large number of mesh lawsuits. We also want to remind women, if you have had the mesh removed you should get the mesh for preservation.

we have been listening to women for months about their mesh complications. Remember a mesh is a mesh:

Transvaginal Mesh,  or pelvic mesh, or  bladder sling, whatever product you want to call it, it is a Prolene mesh. The goal of our mesh helpline has been to reach any woman who has suffered a severe injury as a result of complications with a mesh Implant and help them file a  Mesh Lawsuit. In addition, husbands, children,and family  members of women may sue for wrongful deat and loss of consortium.  We want to hear from you.

 

 

 

 

 

 

FDA Approves Over The Counter Medication For Overactive Bladder, Vaginal Mesh Helpline Reports

Written by Vaginal Mesh Helpline on . Posted in Medical News and Your Vaginal Mesh, Vaginal Mesh News

At the Vaginalmeshhelpline.com we are always looking for new information to help our readers injured by the vaginal mesh. Many women have had the mesh implanted for urinary  incontinence. We just found this online and are sharing it. The FDA has  approved  Oxytrol for women.  This is an over-the-counter Oxytrol treatment for overactive Bladder. Of course we suggest discussing this with your doctor.

January, 25, 2013 — The U.S. Food and Drug Administration today approved Oxytrol for Women, the first over-the-counter treatment for overactive bladder in women ages 18 years and older.

Oxytrol will remain available for men with overactive bladder by prescription only.

Overactive bladder is a condition in which the bladder squeezes too often or squeezes without warning. Symptoms include leaking urine (urinary incontinence), feeling the sudden and urgent need to urinate, and frequent urination. Overactive bladder affects an estimated 33 million Americans, the majority of whom are older women.

Oxytrol for Women contains oxybutynin, a medicine that helps relax the bladder muscle. Oxybutynin belongs to a class of drugs known as anticholinergics. It is the first drug in this class to be made available over-the-counter for treatment of overactive bladder.

Oxytrol for Women is a patch that is applied to the skin every four days. The patch delivers 3.9 milligrams of oxybutynin per day.

 

“Studies demonstrate that over-the-counter Oxytrol for Women is a safe and effective treatment for overactive bladder,” said Shaw Chen, M.D., Ph.D., deputy director of the Office of Drug Evaluation IV in the FDA’s Center for Drug Evaluation and Research. “Women should make sure to follow the Drug Facts label and consult their doctor if their condition does not improve.”

 

Oxytrol for Women’s safety and effectiveness for over-the-counter use were established in more than 5,000 subjects participating in nine studies. Overall, results from these studies showed that consumers can understand the information on the label, properly select whether the product is right for them, and use the drug appropriately.

Side effects reported during clinical studies were mild and included skin irritation where the patch was applied, dry mouth and constipation. A leaflet with tips to help manage overactive bladder will be provided with the product.

Oxytrol for Women is marketed by Merck, based in Whitehouse Station, N.J.

Source: FDA

Posted: January 2013

Vaginal Mesh Trials Have Begun. Vaginal Mesh Lawyers Ready

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh Lawsuits.

The Vaginal Mesh Helpline is keeping you updated on  new news regarding the Vaginal Mesh lawsuits. The vaginal mesh trials have begun. We are waiting, watching and hoping for justice for the thousands of women injured by all these Prolene mesh implants. The stories of pain and suffering we hear on a daily basis are horrific.

We must reach out to all women with a vaginal mesh to push you to file your vaginal mesh lawsuit now.

Have You Been Rejected By A Lawyer Due To Statute Of Limitation Issues?

Call the Vaginal Mesh Helpline. We may be able to get a lawyer for you. Yes, there are statutes of limitations for your state but, there are aspects of the law that may bypass these.  We do not want anyone to be left out. If you have been told by a lawyer that you do not meet “his” criteria do not give up. Call us and get another opinion. There are so many lawyers after mesh victims and as the trials proceed new allegations, criteria and injuries will start to be revealed. What was no 6 months ago maybe yes now. Do not give up hope and call us today.

You Must File Your Vaginal Mesh Lawsuit Now.

The vaginal mesh lawsuits are being filed against five separate manufacturers. They are Johnson & Johnson’s Ethicon division, Coloplast, American Medical Systems, C.R. Bard, and Boston Scientific.

Vaginal Mesh Lawsuit Settlements

The first vaginal mesh trial against Johnson & Johnson  has begun. In March, the nation’s first trial involving an Ethicon mesh lawsuit concluded in the New Jersey litigation, with the jury awarding more than $11 million to the victim, including $7.76 million in punitive damages. (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey).

File Your Vaginal Mesh Lawsuit

If you have not filed your vaginal mesh lawsuit or have been rejected by a law firm based on His “criteria” or statute of limitations call the Vaginal Mesh Helpline today, We may be able to get you a vaginal mesh lawyer and a vaginal mesh doctor.

Vaginal Mesh News Update

A Joint Status Conference is scheduled for May 23rd regarding the thousands of transvaginal mesh lawsuits pending in U.S. District Court for the Southern District of West Virginia. The lawsuits have been formulated into five MDLs, which are entitled: In Re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2325; In Re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation, MDL No. 2326; In Re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2187; and In Re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation, MDL No. 2327.