Posts Tagged ‘California’

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.

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.

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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

FDA Approves Botox For Urinary Incontinence, News For Vaginal Mesh Complications

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News, Vaginal Mesh Stories, Vaginal Mesh lawyers

The Vaginal Mesh Helpline is keeping you up to date on all news related to vaginal mesh lawsuits, Incontinence and vaginal mesh complications and trial updates. This new FDA approval of Botox for urinary incontinence is very interesting. Many mesh victims are seeing incontinence return with the vaginal mesh failing and falling apart.  This news on Botox may be of interest to our vaginal mesh readers.

January 18, 2013 — The U.S. Food and Drug Administration today expanded the approved use of Botox (onabotulinumtoxinA) to treat adults with overactive bladder who cannot use or do not adequately respond to a class of medications known as anticholinergics.

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.

When Botox is injected into the bladder muscle, it causes the bladder to relax, increasing the bladder’s storage capacity and reducing episodes of urinary incontinence. Injecting the bladder with Botox is performed using cystoscopy, a procedure that allows a doctor to visualize the interior of the bladder while Botox is being injected.

“Clinical studies have demonstrated Botox’s ability to significantly reduce the frequency of urinary incontinence,” said Hylton V. Joffe, M.D., director of the Division of Reproductive and Urologic Products in FDA’s Center for Drug Evaluation and Research. “Today’s approval provides an important additional treatment option for patients with overactive bladder, a condition that affects an estimated 33 million men and women in the United States.”

Botox’s safety and effectiveness for this new indication were established in two clinical trials of 1,105 patients with symptoms of overactive bladder. Patients were randomly assigned to receive injections of 100 units of Botox (20 injections of 5 units each) or placebo.

Results after 12 weeks showed that patients treated with Botox experienced urinary incontinence an average of 1.6 to 1.9 times less per day than patients treated with placebo. Botox-treated patients also needed to urinate on average 1.0 to 1.7 times less per day and expelled an average of about 30 milliliters more urine than those treated with placebo.

Treatment with Botox can be repeated when the benefits from the previous treatment have decreased, but there should be at least 12 weeks between treatments.

Side Effects.

Keep in mind that this could be beneficial or prove to have complications down the road.

Common side effects reported during clinical trials included urinary tract infections, painful urination, and incomplete emptying of the bladder (urinary retention). Patients who develop urinary retention may need to use a catheter until the urinary retention resolves. Patients being treated for overactive bladder with Botox should not have a urinary tract infection and should take antibiotics before, during, and for a few days after Botox treatment to lower the chance of developing an infection from the procedure.

Botox is manufactured by Allergan Inc. based in Irvine, Calif.

Mesh Patch Legal Center, Vaginal Mesh Lawyers, Vaginal Mesh Helpline, Vaginal Mesh Case Rejected?

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

Vaginal mesh lawyers, mesh patch legal centers, email blasts, T.V ads and solicitations and they are all after you. Yet, you are in pain. The worst thing is to have your case rejected after months. You are frightened and your marriage is falling apart and you cannot find a doctor whi can help. What is going on? What are these mesh all about and why are the layers all after me? Why cant I find a doctor to remove this? Why hasn’t the FDA done anything to protect us. There are over 300,000 women with a vaginal mesh of some sort implanted in their pelvis.

What is A Vaginal Mesh ?

A mesh is a Prolene synthetic woven device implanted in your pelvis for a prolapse or unrinary incontinence. It was hoped ot would support slackened vaginal wall muscles and relieve incontinence and prolapse. But, these mesh are falling apart. yes, that is right. The are literally disintegrating inside you and when they do this the severe pain of sharp piece of Prolene  to eroding thru you vaginal wall starts. You go to your doctor. Some of the stories we have heard regarding how these doctors respond is amazing.

Now you have:

  • Pain
  • Pain on one side of your body
  • gastrointesitinal problems
  • Urinary incontinence back
  • prolapse back
  • and more

Life has turned full circle and the lawyers are chasing you down. The email blasts are going out in mass. Why? Because with so many women with a mesh and the lawsuits moving in high speed there is a chance they will find you. These email blasts are all leads companies who are selling you to lawyers. This goes for $300 to $700 a mesh. Do these leads companies help you find a doctor? No, they do not. That is not their role. They are there to sell you to a lawyer who will make a file for you and then send your case to the MDL in West Virginia, most likely, and wait for the payoff. Usually if you call the office they have no answers for you and know very little about your agony.

They sometimes even tell you to get your own medical records. beware these email blasts. Know who is behind them. Remember you can switch your lawyer anytime you want to at no loss to you at all.

Where are the mesh cases ending up?

You do not need a local lawyer for your vaginal mesh lawsuit. The transvaginal mesh lawsuits are all part of what is called a centralized or consolidated MDL ( multi district litigation ). The prime one is West Virginia. Your case ,will most likely, end up there. There are only about 60 lawyers is the country actually on the floor in the MDL. The lawyer you retain is your liason to the MDL, in a sense. You must choose wisely and carefully. Choose a lawyer who is responsive and who you feel is answering your questions, Choose one who will help you with the medical aspects. Do not fear if your case is rejected. Many lawyers have very different criteria.

Call the Vaginal Mesh Helpline today.