Class Action Article

  • Physiomesh Hernia Mesh Lawyers: Physiomesh Hernia Mesh lawyers are filing Hernia Mesh lawsuits for your failed Physiomesh used to repair your hernia. Ethicon voluntarily withdrew the Physiomesh from the  market in May of 2016  after independent studies revealed high rates...

Class Action News

  • Stryker Femoral Heads Hip Replacement Lawyers: Stryker V40 Taper Hip Replacement Lawyers Stryker Hip Replacement Lawyers Hip Implant lawyers are filing hip replacement lawsuits for V40 Femoral head failure in the Stryker Hip Implant. In August 2016, Stryker contacted implanting physic...

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

  • File An IVC Filter Lawsuit: Our IVC Filter lawyers are filing IVC Filter lawsuits for injury and Death from a fractured migrating IVC Filter part. The IVC Filters, also known as blood clot filters, Blood Clot Capture Filters and Inferior Vena Cava Filters, are implant...

Posts Tagged ‘Florida’

Stryker Femoral Heads Hip Replacement Lawyers

Written by lisaspitzer on . Posted in Class MDL Class Action News, Stryker femoral head hip Implant lawyer

Stryker V40 Taper Hip Replacement Lawyers Stryker Hip Replacement Lawyers

Hip Implant lawyers are filing hip replacement lawsuits for V40 Femoral head failure in the Stryker Hip Implant. In August 2016, Stryker contacted implanting physicians about metal wear associated with its V40 Taper when used with some cobalt chromium heads.Stryker Orthopaedics sent an Urgent Medical Device Recall Notification to orthopedic surgeons. The recall involves certain sizes of LIFT™ Anatomic CoCr V40™ Femoral Heads manufactured prior to 2011. If you had a LIFT- V40 Femoral Head implanted during total hip replacement, you should be watching for a letter from your surgeon in the next few weeks. You may also be getting a letter from Stryker or a company hired by Stryker to handle claims.

 Stryker Recall Metal V 40 Femoral Heads Lawsuits

Stryker has voluntarily recalled some of their metal V40 femoral heads used with hip implants. Stryker hip replacement lawyers are interested in speaking to anyone with a failed: Exeter, Citation, Meridian, Reliance, Definition, Restoration, Accolade Rejuvenate ABG 2 stems.

This failure may be due to the problems with the V40 femoral head.

The failure of these heads is caused by corrosion and metal debris at the junction between the metal head and neck. The clinical results for patients include pain, loss of mobility, ambulation problems and an inability to work. Poisoning of the soft tissue, muscle and bone are the cause. Revision surgeries may be needed due to premature failures. Stryker lawyers  are seeking patients with  LFit V40 femoral heads made before 2011.

What Is The Femoral Head  Problem?

This is a ball for total hip replacements that can be attached to hip stems, including the Accolade TMZF, Accolade 2, Meridian, and Citation. There have been numerous incidents  of taper lock failures on LFit V40 femoral heads made before 2011,  This taper lock connects the “ball” part of the hip joint to the  hip stem that is inserted in the femur. When it breaks the femoral head will detach from the femoral neck.

Get A Stryker Hip Implant Lawyer

Our Stryker Hip Replacement lawyers are currently accepting Stryker LFit V40 failure cases.

Multi District Litigation Requested For Invokana

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Anaheim, Atlanta, Baltimore, Charleston, Charlotte, Class MDL Class Action News, Dallas, Denver, Fort Lauderdale, Houston, Invokana lawsuit, Invokana lawyer, Invokana Lawyers, Kansas city, Ketoacidosis Lawyer, Las Vegas, Los Angeles, Louisville, Macon, Miami, Minneapolis, North Carolina Multidistrict Litigation Lawyers, NYC, NYC Class Action Lawyers, Philadelphia, Phoenix, Provo, Raleigh-Durham, Reno, Sarasota, Seattle, st louis, Toledo, West Palm Beach, Xarelto Lawyer, Xarelto Lawyers

A Multi District Litigation has been requested for the consolidation of the Invokana lawsuits by Invokana lawyers as lawsuits continue to increase. A consolidation is requested to facilitate proceeding under one judge and jurisdiction. The  lawsuits against the manufacturer of the diabetes drug Invokana are alleging serious injuries after taking Invokana, including heart attack, kidney damage and a dangerous blood condition known as ketoacidosis. The  lawsuits claim that  Johnson & Johnson and its  subsidiary Janssen failed to warn patients and doctors  about the risks of taking Invokana. Invokana lawyers filed a  motion on September 20 asking the U.S. Judicial Panel on Multidistrict Litigation to  consolidate Invokana lawsuits. The formation of an MDL would transfer all cases to a single judge and jurisdiction. Invikana lawyers explained in the motion that the  FDA had received many reports of kidney damage as a result of patients taking Invokana, which led the FDA to issue a stronger  Invokana warning risk with a June 2016 label change. That warning was preceded by another label change in May 2015, alerting users to the risk of ketoacidosi. Ketoacidoasis can be a life-threatening condition that occurs when blood acids known as ketones reach dangerously high levels. Additional warnings were added to the label in August 2016, noting that fatal cases of ketoacidosis had been reported with Invokana use. What Is Invokana? Invokana is a diabetes drug in the   SGLT2 inhibitor category. It  regulate blood sugar levels by encouraging the body to eliminate extra glucose in urine. Consolidation has been requested for the  District Court of New Jersey in Trenton, where 36 of the Invokana lawsuits are already pending. All of those cases are before Judge Brian R. Martinotti, a federal judge the motion notes has extensive experience with complex litigation. If you or a loved one has  had a life threatening event due to Invokana call out Invokana Helpline today.  

Risperdal Lawyer For Gynecomastia Lawsuits Young Boys With Enlarged Breasts From Risperdal

Written by lisaspitzer on . Posted in Drug Lawsuits, Drug Warnings, Risperdal Lawyers

Class Action Lawyer Network Risperdal  Lawyers Filing Lawsuits For  Enlarged Breasts (Gynecomastia) in Young Men From Risperdal

A number of lawsuits  have  been filed alleging  the use of Risperdal  cauded  enlarged breast tissue in young men. Johnson & Johnson has already settled the first of over 100 Risperdal gynecomastia lawsuits. If your son was a victim of Risperdal and it caused severe emotional harm and medical, surgical intervention call and speak to one of our Risperdal lawyers today.

Risperdal Has Been l Linked to Gynecomastia

Risperdal is an antipsychotic medication manufactured by Johnson & Johnson used to treat psychiatric disorders. Young boys on this medication have severe psychological problems.  Using Risperdal may lead to breast growth in men, or gynecomastia.  The result is  severe emotional and medical problems including:

    Swelling

    Pain

    Tenderness

    Nipple discharge in one or both breasts

    The need for surgery for breast reduction

    Psychological effects including suicidal ideation

If Your Son Has Been A Victim The Choice Is Clear

 

If you or a loved one took Risperdal and suffered from gynecomastia or other potential side effects you must consider filing a lawsuit against the manufacturer. Call and speak to one of our Risperdal attorneys

Actos Lawsuit Update

Written by lisaspitzer on . Posted in Actos Lawsuit Lawyers, Drug Lawsuits, Florida Multidistrict Litigation Lawyers, Maine Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, New Hampshire Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, North Carolina Multidistrict Litigation Lawyers, Rhode Island Multidistrict Litigation Lawyers, South Carolina Multidistrict Litigation Lawyers, Washington DC Multidistrict Litigation Lawyers, Washington Multidistrict Litigation Lawyers, Wisconsin Multidistrict Litigation Lawyers, Wyoming Multidistrict Litigation Lawyers

Actos is a medication taken by Type II  ( adult onset ) diabetics to control their insulin production. Actos lawsuits are being filed for victims of bladder cancer from Actos.

Actos Lawsuit Update

 Actos lawsuits that allege long-term use of the Type 2 diabetes drug caused patients to develop bladder cancer continue to move forward in a multidistrict litigation underway in U.S. District Court, Western District of Louisiana. According to court documents, the proceeding’s next Case Management Conference will be held on Thursday, October 24, 2013, at 10:30 a.m. (In re: Actos Product Liability Litigation, MDL No. 2299)

Actos Lawsuit News

According to court documents Actos litigation involving bladder cancer allegations got underway shortly after the U.S. Food & Drug Administration (FDA) warned in June 2011 that use of the drug for 12 months or more had been associated with an increased risk of the disease. At that time, the FDA ordered Takeda Pharmaceuticals to add new warnings to the Actos label about its potential to cause bladder cancer.
Court filings indicate that more than 2,500 Actos lawsuits are now pending in the Western District of Louisiana, where the first case will go to trial in January. Plaintiffs in Actos lawsuits allege that Takeda Pharmaceuticals and other defendants concealed knowledge that the medication could increase a person’s chances of developing bladder cancer, and failed to provide adequate warnings about that risk to the public and medical community.
On the state level, two Actos claims involving bladder cancer allegations have already gone to trial. Last month, a Maryland State Court jury awarded $1.7 million to the family of a man who died of bladder cancer following long-term use of Actos. However, according to court records, the judge presiding over the trial tossed out the verdict because the jury also found that the decedent’s decades-long smoking habit contributed to the development of the disease. (An v. Nieberlein, 24-C12003565, Circuit Court for the City of Baltimore, State of Maryland.)
This past April, a Los Angeles Superior Court jury awarded $6.5 million to a plaintiff who developed bladder cancer following four years of Actos use. However, the plaintiff is currently appealing a decision by the judge overseeing the case to grant Takeda Pharmaceuticals’ request to set aside the verdict. (Cooper v. Takeda Pharmaceuticals America Inc., CGC-12-518535, California Superior Court)
Long-term users of Actos ( over 2 years ) who have been diagnosed with bladder cancer may be eligible to file an Actos lawsuit against Takeda Pharmaceuticals.

Actos Lawsuit Criteria

1. You must have taken Actos for over two years

2. You must have a confirmed diagnosis of bladder cancer

3. You must have no prior medical history of baldder cancer prior to taking Actos

Resperdal Class Action Lawyers, Resperdal Lawsuit Helpline

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Arizona Multidistrict Litigation Lawyers, Arkansas Multidistrict Litigation Lawyers, California Multidistrict Litigation Lawyers, Colorado Multidistrict Litigation Lawyers, Delaware Multidistrict Litigation Lawyers, Drug Lawsuits, Florida Multidistrict Litigation Lawyers, Georgia Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Kansas Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, Ohio Multidistrict Litigation Lawyers, Resperdal lawsuits

Risperdal Lawyers Filing Gynecomastia Lawsuits

If you or a loved one was prescribed Risperdal as a teenage boy and now have enlarged breasts, developed female type breasts and /or been diagnosed with Gynecomastia,  contact Class Action Lawyer Network  Risperdal Injury Lawyers today to discuss your options in a Risperdal lawsuit.

Our Resperdal lawyers are reviewing cases for young  boys diagnosed with gynecomastia or male breasts after using Risperdal. Problems may result in:

  •     Breast Growth Among Boys
  •     Puffy Nipples or Enlarged Nipples
  •     Galactorrhea (production of milk from breasts)
  •     Painful Breasts or Nipple Discharge
  •     Mastectomy or Gynecomastia Surgery to Remove Male Breasts
  •     Gynecomastia (growth of male breasts, which may be painful or tender)

If your son has been diagnosed with Gynacomastia call our Resperdal helpline and speak to our trained medical social worker today.

Rispedral Side Effects In Male Children

Risperdal (risperidone) is an antipsychotic manufactured by Johnson & Johnson. It  was originally approved by the FDA for use for adults with schizophrenia.  Risperdal has also been widely used by children for bi-polar disorders, autism, irritability, aggression and behavior disorders.

Speak To A Risperdal Lawyer

The Riserdal  lawyers are reviewing cases for Risperdal breast growth among boys.

Children Are Being Injured By Risperdal

Lawsuits are being filed  for  abnormal development of large mammary glands among boys and adolescents, resulting in breast development.  Surgery has been  necessary to remove the breasts caused by the Risperdal gynecomastia.  This has caused emotional trauma for boys and young adult males and some incidents of suicide. Parents throughout the United States are pursuing a Rispedal lawsuit on behalf of kchildren  who developed breasts on Risperdal.

Lawsuits allege that Johnson & Johnson failed to adequately research the effects of their medication or warn about the connection between Risperdal and breast growth.

Risperdal Lawsuit Update

Although Resperdal is not currently an MDL, settlements for Risperdal breast growth have been reached by Johnson & Johnson in lawsuits bellwether trials where a number of cases are presented to juries to test the potential settlements and outcomes. Do not delay. Call no to discuss a Resperdal lawsuit.
 

 

 

Nationwide Bladder Sling Lawyer Outreach, Bladder Sling Lawsuits Being Filed

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

Bladder Sling Lawyers, Bladder Sling Lawyers Filing Nationwide Bladder Sling Lawsuits

The bladder sling lawyers of Class Action Lawyer Network are accepting all nationwide bladder sling lawsuits. Lawsuits are being filed as a part of the consolidated MDL'S in West Virginia.

What Is A Bladder Sling?

Bladder slings are used to treat urinary incontinence by implanting  a sling around the urethra. The bladder sling is attached to the abdominal wall or pelvic bone. The bladder sling is a vaginal mesh device, and has all the complications for which TVT lawsuits are being filed.

Bladder Sling Complications

Erosion thru the vaginal wall 

Erosion into the bladder,

Pain during sexual intercourse,

Bleeding,

Infection,

Perforation of bladder, colon,

Urinary incontinence

Problems voiding.

Our bladder sling lawyers are  filing bladder sling lawsuits for  women. You must file a bladder sling lawsuit quickly, as the statute of limitations is running very close in many states.

 The manufacturers are:

    Bard Avaulta Support System MDL No. 2187

    AMS Elevate Prolapse Repair System MDL No. 2325

    AMS Apogee Vault Suspension System

    AMS Perigee System

    AMS Monarc Sling System

    AMS Sparc Sling System

    Ethicon Gynecare Gynemesh MDL No. 2327

    Ethicon Gynecare Prolene Soft Mesh

    Ethicon Gynecare Prolift Pelvic Floor Repair System

    Ethicon Gynecare TVT Transvaginal Sling

    Boston Scientific Pinnacle Pelvic Floor Repair Kit MDL No.2326

    Boston Scientific Uphold Vaginal Support System

Vaginal Mesh Multi District Lawsuit List Consolidated Under Judge Goodwin in West Virginia

    MDL – 2325, IN RE: American Medical Systems, Inc., Pelvic Repair System Products Liability Litigation
    MDL No. 2187 | In RE: CR Bard, Inc., Pelvic Repair System Products Liability Litigation
    MDL – 2326 IN RE: Boston Scientific Corp. Pelvic Repair System Products Liability Litigation
    MDL – 2327 IN RE: Ethicon, Inc., Pelvic Repair System Products Liability Litigation
 

Our experienced bladder sling lawyes ready to file bladder sling lawsuits  slings problem lawsuits.  Vaginal mesh products have many different names. Do not assume your bladder sling is not covered in the TVT lawsuits  until you speak to one of our bladder sling  lawyers. Many states have a  statue of limitations issue. Time is of the essence. Call our nationwide bladder sling lawyers today.

Did You Take Yaz Or Yasmin? Settlements For Yaz Lawsuits For Bloodclots

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

Yaz, Yasmin Lawsuit  Multidistrict Litigation


MDL 2100 – Yasmin and YAZ (Drospirenone) Marketing, Sales Practices and Products Liability Litigation, multidistrict litigation (MDL) in Illinois federal court.


Yaz lawyers are accepting Yaz lawsuits for blood clot related injuries:

  • Pulmonary Embolism
  • Blood Clots
  • Stokes
  • Deep Vein Thrombosis

Bayer is facing thousands of Yaz and Yasmin lawsuits involving blood clot related injuries.

Yaz Blood Clot Settlements

According to Bayer’s 2nd Quarter 2013 Statement, Bayer  haa agreed to pay more than $1.4 billion to resolve an estimated 6,700 lawsuits from women  who suffered a:
    Heart attack or Stroke from Yaz or Yasmin
    Pulmonary Embolism from Yaz or Yasmin
    Deep Vein Thrombosis from Yaz or Yasmin

There are still  more than 5,000 additional claims involving a thrombosis blood clot related injury.  Bayer is continuing negotiating on a case-by-case basis, after complete documentation and presentation of the claim by an attorney. It is not too late to file your Yaz blood clot lawsuit. Our Yaz lawyers are still  continuing to review and evaluate potential claims from women who suffered a pulmonary embolism, deep vein thrombosis, heart attack, stroke or other blood clot injury while using Yaz, Yasmin or Ocella.

If you or a loved one has been injured by Yaz or a loved one has died from a Yaz related injury call us for a Yaz lawyer today.
 

Vaginal Mesh Bellwether Trials Updated

Written by lisaspitzer on . Posted in Arkansas Multidistrict Litigation Lawyers, Class MDL Class Action News, Connecticut Multidistrict Litigation Lawyers, Florida Multidistrict Litigation Lawyers, Maine Multidistrict Litigation Lawyers, Maryland Multidistrict Litigation Lawyers, Medical Device Lawsuits, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, New Hampshire Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, North Dakota Multidistrict Litigation Lawyers, Pennsylvania Multidistrict Litigation Lawyers, Rhode Island Multidistrict Litigation Lawyers, South Carolina Multidistrict Litigation Lawyers, South Dakota Multidistrict Litigation Lawyers, Washington DC Multidistrict Litigation Lawyers, Washington Multidistrict Litigation Lawyers, West Virginia Multidistrict Litigation Lawyers, Wisconsin Multidistrict Litigation Lawyers, Wyoming Multidistrict Litigation Lawyers

Get Your  Mesh lawsuit Attorney Today

Vaginal Mesh Lawsuit Updates

The vaginal mesh Class action ( multi-distict litigation ) may very well be the largest since the Dow Corning Breast Implant Class Action. The bellwether trials are progressing. Below are the updated reports. A bellwether trial sets the tone of expectation for a juries reaction to injuries, So far the juries have spoken in favor of the victims.

Bard Bellwether Trial, The First of Four Bellwether Trials

A jury  found C.R. Bard iiable for injuries and  must pay $2 million to a woman who sued saying she suffered injuries from the company’s vaginal-mesh implant, a jury found. Today’s jury verdict in Charleston, West Virginia, was the first in a federal court out of more than 5,000 claims over the devices. Jurors deliberated about 12 hours over two days before finding Murray Hill-based Bard liable for injuries that Donna Cisson blamed on its Avaulta line of devices. The jury awarded $250,000 in compensatory damages for Cisson’s injuries plus $1.75 million in punitive damages.

Boston Scientific Next

The first Boston Scientific  round of trials will begin on February 11, 2014, and will involve lawsuits filed over injuries  related to the use of the Pinnacle mesh products.
The second round will start on June 17, 2014, and will involve cases brought against Obtryx pelvic mesh. (In re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation – MDL No. 2326)

Boston Scientific is just one of several manufacturers involved in litigations for surgical mesh lawsuits established in the Southern District of West Virginia.

Johnson and Johnson Trial Updates

A jury in Atlantic City ordered Johnson & Johnson’s Ethicon unit to pay $11.1 million to a woman who suffered severe injuries from its vaginal mesh device.

Vaginal Mesh Overview

C.R. Bard’s products include:

Bard Pelvitex
Bard Pelvisoft
Bard Pelvilace or Pelvicol
Bard Utrtex
Bard Uretex TO
Bard Uretex TOO2
Bard Uretex TOO3

Bard Align
Avaulta Plus™
Avaulta Solo™
BioSynthetic Support System
Faslata® Allograft
Synthetic Support System

Coloplast Vaginal Mesh Products

    Novasilk Synthetic Flat Mesh
    Restorelle Smartmesh
    Exair Mesh

  
Johnson & Johnson products include:

Gynecare Prosima
Gynecare TVT Exact
Gynecare TVT Abbrevo
Gynecare TVT Retropubic System
Gynecare TVT
Gynecare TVT Obturator
Gynecare TVT Secur
Gynecare Gynemesh PS
Gynecare Prolift
Gynecare Prolift+M

Cook Medical Surgical Products

    Cook Medical Surgical
    Surgisis Biodesign Tension-Free Urethral Sling,
    Surgisis Biodesign
    Anterior Pelvic Floor Graft,
    Surgisis Biodesign Posterior Pelvic Floor Graft,
    Cook Urological Stratasis

AMS’s products include:

AMS MiniArc Precise Single-Incision Sling
AMS MiniArc Single Incision Sling
AMS Monarc Subfascial Hammock
AMS In-Fast Ultra Transvaginal Sling
AMS BioArc
AMS Sparc Self-Fixating Sling System
AMS Elevate
AMS Perigree
AMS Apogee
  
Boston Scientific products include:

Boston Scientific Arise
Boston Scientific Pinnacle
Boston Scientific Advantage Fit
Boston Scientific Lynx
Boston Scientific Obtryx
Boston Scientific Prefyx PPS
Boston Scientific Solyx

Vaginal Mesh Multi District Lawsuit List Consolidated Under Judge Goodwin in West Virginia

    MDL – 2325, IN RE: American Medical Systems, Inc., Pelvic Repair System Products Liability Litigation
    MDL No. 2187 | In RE: CR Bard, Inc., Pelvic Repair System Products Liability Litigation
    MDL – 2326 IN RE: Boston Scientific Corp. Pelvic Repair System Products Liability Litigation
    MDL – 2327 IN RE: Ethicon, Inc., Pelvic Repair System Products Liability Litigation
    MDL – 2387 IN RE: Coloplast Corp. Pelvic Support Systems Products Liability Litigation
    Cook Medical Surgical will be the 5th MDL

Vaginal Mesh Bellwether Trials

Vaginal Mesh bellwether trials are selected to determine how similar vaginal mesh  lawsuits might turn out for the victims.  It’s a chance to see how juries will respond to the injury  claims when there are a large number of lawsuits with similar complaints. This  is very important to our vaginal mesh  lawyers.

 

Tylenol Lawsuits For Liver Damage Multi District Litigation Consolidation

Written by lisaspitzer on . Posted in Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Class Action Lawyer Network Tylenol liver damage lawyers report that tylenol liver failure  lawsuits will be centralized in a multidistrict litigation in Pennsylvania  Federal Court,

Tylenol Lawsuit Consolidated In Pennsylvania

All Tylenol liver damage  lawsuits filed against McNeil-PPC, Perrigo, Novartis and others have  been consolidated under multidistrict litigation in the Eastern District of Pennsylvania to facilitate the pretrial proceedings for  these cases

The U.S. Judicial Panel on Multidistrict Litigation (MDL) has ruled that 27 Tylenol liver damage lawsuits filed against  the manufacturers of tylenol related products will be consolidated under Tylenol Lawsuit MDL 2436 in the Eastern District of Pennsylvania.
All of the cases conslidated in MDL 2436 involve liver damge related injury or wrongful death. These  claims alledged that use of over-the-counter (OTC) Tylenol (generically acetaminophen) caused the victims to suffer from serious liver damage or  liver failure.

Call Class Action Lawyer Network's Tylenol Liver Damage Lawsuit Department Today.

The MDL  Judicial Panel feel that the  allegations of liver injury associated with the use of OTC Tylenol, the cases share factual issues regarding the design, manufacture, labeling, marketing and sale of Tylenol. Consequently, the centralization of these cases in the Eastern District of Pennsylvania would eliminate duplicative discovery facilitate the proceedings.

Class Action Lawyer Nwtwork  attorneys  have decades of collective dangerous drig  and device lawsuit experience,

If you or a loved one has suffered liver damage or liver failure while taking Tylenol call us to discuss a Tylenol liver damage lawsuit or Tylenol liver failure lawsuit.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with Liver Failure, liver damage from taking Tylenol? Do you have a clean medical history of any liver problems such as: Liver cancer, liver mass, Autoimmune Hepatitis, Alcoholic Cirrhosis,Primary Sclerosing Colangitis, Wilson’s disease, or Budd Chiari Syndrome  and yet,  now have liver damage after taking Tylenol?
Our Tylenol liver damage lawyers are accepting Tylenol liver failure cases  if  the liver failure results in hospitalization, liver transplant, or liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage or liver failure case.

Class Action Lawyer Network  accepting Tylenol liver damage lawsuts  or liver failure  lawsuits for individuals who experienced  any of the following within a week after taking  an acetaminophen medication such as Tylenol:

  •     Hospitalization Due to Severe Liver Injury or Liver Problems
  •     Diagnosed with Liver Failure
  •     Liver Transplant or Placed on Waiting List for Liver Transplant
  •     Death from Liver Failure

Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuits

Written by lisaspitzer on . Posted in Class MDL Class Action News, Drug Lawsuits, Drug Warnings, Florida Multidistrict Litigation Lawyers, Tylenol Liver Damage Lawsuits, Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Tylenol Liver Damage Lawyers of Class Action Lawyer Network Are Filing  Nationwide Tylenol Liver Failure  Lawsuits

The Tylenol liver damage lawyers of Class Action Lawyer Network are accepting nationwide lawsuits for you , your loved one or child who has suffered liver damage from Tylenol. Our Tylenol Liver Damage Helpline is helping victims of liver damage from Tylenol.

The Tylenol Liver Damage Facts

It is now known that Tylenol can result in acute liver failure and death. Statistics have shown taht  Tylenol is the leading cause of acute liver failure in the United States; nearly half of U.S. incidents of acute liver failure are caused by  taking too much acetaminophen. Acetaminophen is anactive ingredient in Tylenool.  Call our Tylenol liver failure  helpline to speak to lawyers help who are filing liver damage lawsuits for victims  of Tylenol who have been diagnosed with Tylenol liver damage or failure.

Symptoms Of Liver Damage

  •     Discolored skin and eyes that appear yellowish
  •     Abdominal pain and swelling
  •     Itchy skin that doesn't seem to go away
  •     Dark urine color
  •     Pale stool color
  •     Bloody or tar-colored stool
  •     Chronic fatigue
  •     Nausea
  •     Loss of appetite
     

Class Action lawyers For Tylenol Liver Failure

  • Tylenol's manufacturer lowered the safe maximum dosage from 4000 mg to 3000 mg per day.
  • Tylenol liver Failure Helpline lawyers are fighting for justice for victims of tylenol Llver damage and liver failure
  • If you or a family member has  been diagnosed with  severe liver damage or acute liver failure from excessive use of Tylenol or other over the counter medications that contain acetaminophen the Tylenol liver damage helpline is here for you.
  • People who have experienced acute liver failure or serious liver damage related to Tylenol use may file a Tylenol liver damage lawsuit  lawsuit

Tylenol Lawsuit Multi District Litigation Has Formed

The  Tylenol injury lawsuits have now been centralized as part of multidistrict litigation in federal district court in Pennsylvania.

The lawsuits filed alledge a strong link between acetaminophen and liver failure. Lawsuits are  alleging that acetaminophen in various Tylenol products was responsible for users’ severe liver damage.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with liver Failure, liver damage or a severe liver injury from taking Tylenol?

Our Tylenol liver damage lawyers are accepting Tylenol liver failure if  the liver failure results in hospitalization, liver transplant, liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage lawsuit where there is no prior medical history of liver damage or any liver damage related medical conditions.
 

Call our Tylenol Liver Damage Helpline to file your liver damge lawsuit.