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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

  • Zimmer Hip Replacement Lawyers: Network Zimmer Hip Replacement  Lawyer Win $2 Million Against Zimmer Hip Replacement Do You Have A Faulty Zimmer M/L Taper Hip Prothesis With Connective Technology and Cobalt Chromium Head? Do You Have Have Metallosis or Chromium Cobalt T...

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File A Talcum Powder Lawsuit

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Alaska Multidistrict Litigation Lawyers, Arizona Multidistrict Litigation Lawyers, Arkansas Multidistrict Litigation Lawyers, California Multidistrict Litigation Lawyers, Class Action Articles, Colorado Multidistrict Litigation Lawyers, Connecticut Multidistrict Litigation Lawyers, Dallas, Delaware Multidistrict Litigation Lawyers, Denver, Detroit, Fallopian tube cancer lawyer, File A Talcum Powder Lawsuit, Florida Multidistrict Litigation Lawyers, Florida vaginal mesh lawsuit, Fort Lauderdale, Georgia Multidistrict Litigation Lawyers, Hawaii Multidistrict Litigation Lawyers, Homedica Recall Lawsuits, Houston, Idaho Multidistrict Litigation Lawyers, Idaho Talcum Powder Lawyer, Illinois Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Iowa Multidistrict Litigation Lawyers, Johnson and Johnson Baby Powder Lawsuit, Kansas city, Kansas Multidistrict Litigation Lawyers, Kentucky Multidistrict Litigation Lawyers, Las Vegas, Little Rock Talcum Powder Lawyer, Louisiana Multidistrict Litigation Lawyers, Louisville, Macon, Maine Multidistrict Litigation Lawyers, Maryland Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Miami, Michigan Multidistrict Litigation Lawyers, Minneapolis, Minnesota Multidistrict Litigation Lawyers, Mississippi Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, Nebraska Multidistrict Litigation Lawyers, Nevada, Nevada Multidistrict Litigation Lawyers, New Hampshire Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, North Carolina Multidistrict Litigation Lawyers, North Dakota Multidistrict Litigation Lawyers, NYC, NYC Class Action Lawyers, Ohio Multidistrict Litigation Lawyers, Oklahoma Multidistrict Litigation Lawyers, Oregon Multidistrict Litigation Lawyers, Ovarian cancer lawyer, Pennsylvania Multidistrict Litigation Lawyers, Philadelphia, Philadelphia Baby powder lawyer, Phoenix, Provo, Raleigh-Durham, Reno, Rhode Island Multidistrict Litigation Lawyers, Sarasota, Seattle, South Carolina Multidistrict Litigation Lawyers, South Dakota Multidistrict Litigation Lawyers, st louis, St Louis Talcum Powder lawyer, Talcum Powder cancer lawyers, Talcum Powder Ovarian cancer lawyer, Tennessee Multidistrict Litigation Lawyers, Texas Multidistrict Litigation Lawyers, Utah Multidistrict Litigation Lawyers, Vermont Multidistrict Litigation Lawyers, Virginia Multidistrict Litigation Lawyers, Washington DC Multidistrict Litigation Lawyers, Washington Multidistrict Litigation Lawyers, West Palm Beach, West Virginia Multidistrict Litigation Lawyers, Wisconsin Multidistrict Litigation Lawyers, Wyoming Multidistrict Litigation Lawyers

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 cancer speak to one of our talcum powder lawyers. Lawsuits are being filed for women who used talcum powder products on or around the genital area for over five years and now have diagnosis of ovarian cancer or fallopian tube cancer.

What Talcum Powder  Products Are In Question?

Talcum powder products such as  Johnson & Johnson’s Baby Powder and Shower to Shower are suspect for causing both ovarian cancer and fallopian tube cancer in women,  These products have been used by women for decades to absorb moisture and for personal hygiene.

Can I File A Talcum Powder Lawsuit?

Women are filing talcum powder cancer  lawsuits against Johnson & Johnson for knowing about the possible risk of ovarian cancer and fallopian tube cancer with the use of their products.  They failed to warn doctors, women and the public. If you or a loved one has been diagnosed with ovarian cancer or fallopian tube cancer after using these products you may be eligible to join other women in a products liability lawsuit.  Complete the form to see if you may qualify for joining the lawsuit.

Lawyers For Stryker Hip Replacement Metal Toxicity- Femoral Head Failure

Written by lisaspitzer on . Posted in Class MDL Class Action News, Stryker Metal Poisoning, Stryker Rejuvinate, Stryker Rejuvinate Hip replacement recall lawyers, Stryker’s Scorpio implant lawyers

Cobalt Chromium Blood Poisoning Stryker Hip Replacement Lawyers

New Stryker Recall Metal V 40 Femoral Heads Lawsuits

Stryker LFIT Femoral Head Failure

Exeter, Citation, Meridian, Reliance, Definition, Restoration, Accolade, Rejuvenate and ABG 2 stems chromium and cobalt toxic levels are resulting in lawsuits due to corrosion and metal debris at the junction between the metal head and neck.

Recall Of  LFIT ANATOMIC COCR V40 FEMORAL HEADS

Metallosis Lawsuits Filed

Metal poisoning, or metal toxicity is the build-up of metal particles  in the body and found in the blood stream. Metal toxicity from a hip implant can be serious.  The metal parts rub against each other  and release particles of  chromium and cobalt, into the blood stream.   Build-up in the body can cause:
  • Renal failure
  • Cardiovascular problems
  • Neurological disorders
  • Hypothyroidism
  • Blindness and deafness
  • Death

Signs Of Elevated Metal Levels

  • headaches,
  • dizziness,
  • loss of eyesight,
  • loss of hearing

Get a  hip implant metallosis lawyer

 

Mesh Lawsuit Alert | Physiomesh – Hernia Mesh Lawyers

Written by lisaspitzer on . Posted in Hernia mesh lawyer, Vaginal mesh lawyer

A New Ethicon Mesh Causes Deaths And Injury

The U.S. Food and Drug Administration (FDA) has atleast 10 reported adverse incident reports of deaths due to a new Ethicon synthetic mesh Device. Ethicon has 100’s of  polypropylene vaginal mesh lawsuits filed for the failed vaginal mesh and bladder sling. The Physiomesh is made with the same substance and is another Ethicon fiasco.  

Mesh  Made Of  Polypropylene-

Vaginal Mesh- Hernia Mesh Lawyers

Physiomesh has increased risks because it was  designed with a lower level of elasticity compared to competing hernia mesh products. This may cause poor attachment to the interior abdominal wall and  retraction/contraction, ripping and failing.  

Complications  of vaginal mesh implant deterioration and failure

Severe pelvic, genital or groin pain. Recurrence of prolapse or incontinence. Nerve damage. Vaginal scarring. Degrading of the mesh. Urinary tract infections Ethicon mesh for vaginal prolapse repair or urinary incontinence or for hernia mesh is causing sever medical complications and lawyers are accepting lawsuits.

Physiomesh Hernia Mesh Lawyers

Written by lisaspitzer on . Posted in Class Action Articles, Physiomesh Hernia Mesh Lawsuit, Physiomesh Lawyer

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 of recurrence and failure from the Physiomesh.

What Is The Physiomesh?

The Physiomesh is a hernia repair mesh  made from polypropylene just like the vaginal mesh products. The FDA originally approved Ethicon’s Physiomesh on April 9, 2010. Ethicon used the FDA 510(k) approval program for the Physiomesh. This allowed them to get it on the market fast.

Problems With The Physiomesh

Numerous studies have shown that the Physiomesh has  lower incorporation strengths than the other hernia mesh products.  Physiomesh coating  issues were observed over time to lead to scar plate formation, but little to no abdominal wall adherence.

Physiomesh: Ethicon Hernia Mesh Lawyers

Speak to a  physiomesh  hernia mesh attorney to discuss a  Physiomesh lawsuit

File An IVC Filter Lawsuit

Written by lisaspitzer on . Posted in Cordis IVC Filter Lawyer, Medical Device Lawsuits

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 implanted in patients that cannot tolerate blood thinners. They capture blood clots before they can become lodged in the brain or lungs causing a stroke  or pulmonary embolism. However, the IVC filter has been proven to be dangerous because it can fracture if left in too long.

 Which Manufacturers Are You Accepting IVC Filter Lawsuits For?

 Our lawyers are accepting  COOK, BARD  or CORDIS IVC Filter Claims.

 Bard IVC Filters Include:

  • – Recovery
  • G2
  • – G2X
  • – Eclipse
  • Meridian
  • – Denali
 COOK IVC Filters Include:
  • – Gunther Tulip
  • – Celect
 CORDIS IVC Filters Include:
  • – OptEase
  • – TrapEase

 Criteria For The IVC Filter Lawsuit

Your Filter must have been implanted in  2002 through present.

REASONS FOR IVC FILTER  IMPLANTATION:

1. Pulmonary embolism (PE) and anticoagulants could not be used in case for some reason
2. Anticoagulants failed to treat/remove blood clot
3. Trauma
4. Bariatric Surgery
5. Orthopedic Surgery
What Were your Injuries Or Complications ?
1. Tilt
2. Migration
3. Fracture
4. IVC perforation
5. Filter embolization
6. Filter unable to be retrieved
 
IF DEATH Due To An IVC Filter
1. Date of Death
2. Location (City & State)
3. Was an autopsy performed?
4. Cause of death listed on autopsy
5. Cause of death listed on death certificate
6. Has an estate been opened? (Name of administrator
HAS FILTER BEEN SUCCESSFULLY REMOVED? (With or without complications)?
  • 1. Date of removal
    2. Symptomatic or asymptomatic at time of removal?
    3. Percutaneous without complication(s) Our lawyers are not taking these cases
    4. Open with or without complication(s)   Our lawyers are taking these cases.
    CT Scan  will be needed for evaluation of claim even if you are  asymptomatic.
    MANUFACTURERS WE ARE NOT TAKING
     
    1. Boston Scientific (Greenfield SS and TI Permanent) We need to be careful in turning
    down Greenfield filter cases because this is a generic term used to describe all IVC
    filters.
    2. B. Braun Medical (Convertible, Vena Tech and LP)
    3. ALN
    4. Rex Medical (Option)
    5. Rafael Medical (SafeFlo)

    Get An IVC Filter Lawyer

    If you or a loved one has been injured or you have lost a loved one due to a Faulty IVC Filter contact us today
 

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.  

Vaginal Mesh Lawsuits, You Must file Before the Statute Is Up

Written by Class Action Lawyer on . Posted in Medical Device Lawsuits

Time to File Depends on the Date of Injury

Statutes of limitations are state laws that require plaintiffs to file their cases within set time periods. Because all defective medical device lawsuits are tort claims, they are covered by state law and not federal law. Any medical device lawsuits before U.S. District Courts are claims brought under state law by plaintiffs from states other than the ones in which the manufacturers are located. The purpose of statutes of limitations is to encourage injured parties to bring their claims in a timely manner to prevent courts from dealing with old records and hazy memories.
vaginal mesh mdl lawsuits image
The amount of time a statute of limitations gives someone to file a claim depends on the type of claim the plaintiff is filing. Commonly, the limitations period for products liability cases is two or three years from the date of injury. When the injury occurred matters significantly from a legal standpoint. Sometimes, the injury “occurs” the day the vaginal mesh was implanted; other times it “occurs” when the plaintiff first knew or could have reasonably found out about the injury. This can be troubling for vaginal mesh recipients because the pain and symptoms of mesh erosion might not occur until long after the initial procedure. Because some women might have already had their vaginal mesh problems resolved years ago and didn’t meet with a Vaginal mesh lawyer, the statute of limitations might have already expired for them, and they will be unable to obtain compensation via a transvaginal mesh lawsuit. If you are having complications ffrom a vaginal mesh it is in your best interests not to wait and file with a lawyer immediately. You must not run the risk of losing your rights to file a lawsuit. The vaginal mesh complications are sever and the mesh implants are ruining lives. You Must send a message and contact a lawyer today. 1 877 522-2123

Vaginal Mesh Lawsuit News Update , Vaginal Mesh Lawyer

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

More than 150 federal lawsuits involving vaginal mesh slings were consolidated in a U.S. District Court in West Virginia. "actions in each MDL share factual issues arising from allegations of defects in pelvic surgical mesh products manufactured by AMS, Boston Scientific, and Ethicon." The cases will be heard in front of one judge who understands the issues.

Ask Questions   Get Answers

Also known as a pelvic sling, bladder mesh, or transvaginal mesh, the vaginal mesh support systems are used to help with pelvic organ prolapse  as well as urinary incontinence  It is now known that they can cause serious internal injuries.  These vaginal mesh patch implants, manufactured by Johnson & Johnson , C.R. Bard, Boston Scientific, American Medical Systems, and others, may cause pain, infection, erosion, organ damage, and additional surgeries, and other vaginal mesh injuries.

If you have experienced vaginal mesh complications following pelvic organ prolapse surgery or stress urinary incontinence surgery, The  vaginal mesh Helpline  will offer support and direct you to a lawyer who   may be able to help you obtain significant compensation for the vaginal mesh problems you are experiencing.

Call us at 1 877 -522-2123 to speak with a female social worker and be directed to a lawyer.

Vaginal Mesh- History of the Problem

Between the years of 2005 and 2010, nearly 4,000 vaginal mesh injuries have been reported to the Food and Drug Administration.  In a 2010 article in the journal Obstetrics & Gynecology, researchers stated that they had to cease a vaginal mesh clinical trial early because of the higher-than-expected number of complications and injuries.  The trial was stopped when it was discovered that more than 15 percent of women who were implanted with vaginal mesh suffered vaginal mesh erosion within only three months of implantation.  As a result of numerous negative reports, the FDA issued a vaginal mesh warning to patients and physicians in 2011, cautioning that the risks of using vaginal mesh are so severe that alternative treatments should be considered.  It is now widely accepted that, in most cases, pelvic organ prolapsed can be treated without the use of vaginal mesh

What are the vaginal Mesh Injuries

    Erosion of vaginal tissue
    Hardening of the vaginal mesh
    Infection
    Pain and discomfort
    Perforations of the bowel, bladder or blood vessels
    Recurrence of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI)
    Urinary problems
    Vaginal mesh erosion
    Vaginal scarring

Many women who have suffered injuries as a result of vaginal mesh have decided to file defective medical device lawsuits. This has become a class  and  class action lawsuits are being filed. An product liability, class action attorney can review your case.

 

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Attorneys who cover Orlando, Winter Park, Winterhaven, Kissimmee,Ocala,Atlamonte Springs,Deland,Melbourne, Daytona. Orange,Osceola,Seminole,Lake,Volusia, Polk and Brevard Counties

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Attorneys who cover Miami, Hialeah, Miami Beach and the Florida Keys including all of Dade and Monroe counties

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Attorneys who cover Tampa, Brandon, Clearwater, St Pete, New Port Richey, Brooksville, Sarasota, Naple, Venice, Bradenton, Fort Myers, Cape Coral and all of Hernanado, Citrus, Pasco, Pinnellas, Hillsboro, Sarasota, Manatee, Lee and Collier counties.

10151 Deerwood Park # 200-250, Jacksonville, FL
Attorneys who cover  Jacksonville, Jacksonville Beach, St. Augustine, Orange Park all of Northeast Florida including Marion Sumter, Flager and Duval counties. Also Attorneys who cover Northwest Florida including: Tallahassee, Pensacola, Panama City and Starke.

233 Peachtree Street N.E., Atlanta, GA 30303
Attorneys who cover Atlanta, Decatur, Roswell, Marietta, Jonesboro, Gainesville, New Smyrna, Fayetteville, Buford, Cartersville, Lilburn, Macon, Augusta, Savanah, and all of Georgia.

1001 G Street NW, Washington, DC 20001

4201 Wilshire Blvd., Los Angeles, CA 90010

Attorney Network class action lawyers of New York, New Jersey, Colorado, Arizona,California, North and South Carolina, Tennessee  Michigan, and Texas

If you have suffered any of the above listed injuries after being implanted with vaginal mesh to remedy a pelvic organ prolapse or urinary incontinence  you may be entitled to  compensation in a dangerous medical device class action litigation.  An experienced medical product liability Attorney will  analyze  your claim and explain your legal rights. Speak to A  female MSW about your  vaginal mesh .
 

Lawyers for Reglan, FDA Warnings for Reglan, Tardive Dyskinesia

Written by Class Action Lawyer on . Posted in Class MDL Class Action News, Drug Warnings

What is Reglan (Metoclopramide)? A. H. Robins Co. Reglan Metoclopramide
Reglan (metoclopramide) is a prescription drug often prescribed to treat gastrointestinal problems in children and adults. Reglan is most often used to control gastroesophageal reflux disease (GERD), or to reduce nausea and vomiting.  Physicians will often use Reglan for both children and adults suffering from reflux, gastroparesis, and other conditions related to the stomach such as heartburn, decreased appetite, and prolonged fullness after eating.  Even infants are sometimes given Reglan for reflux.
Reglan works by affecting the lower esophageal sphincter pressure, which then helps to improve gastrointestinal emptying.  The FDA has only approved Reglan for short-term treatment (between 4 and 12 weeks) of these conditions, and  only after conservative methods of treatment have failed.  Unfortunately, prescription trends prove that many patients are prescribed Reglan for longer than 12 weeks (often for years), which is against FDA recommendations.  The manufacturers of Reglan are well aware of these extended prescription trends.
Medical science and studies have proven that Reglan can cause Tardive Dyskinesia, a serious and often irreversible movement disorder.  Infants who are given Reglan appear to be at an even greater risk for this serious drug side effect.

FDA Issues Advisory for Reglan
In February 2009, the FDA issued an advisory, that forces the manufacturers of Reglan (MCP) to update their label. The advisory calls for a "black box" warning – the strongest warning that the FDA can issue. The advisory (and the proposed black box warning) are attached here … In addition, the FDA has requested that the drug companies send Dear Doctor letters – enclosing the new label and the new warning. This also is one of the strongest ways the FDA can spread the word – both to doctors and to patients taking Reglan.

What is GERD or Reflux?
For infants, it is often called reflux, short for the medical term gastroesophageal reflux (GER).  It is a common condition in infants, and typically resolves between six and twelve months of age.  Infants with reflux will often spit up after feeding, and have difficulties taking in enough nutrition.  Many babies suffer from reflux, and rarely need treatment.  Some, however, do receive Reglan for treatment.
For adults, the symptoms usually progress to a greater set of problems, such as chronic heartburn, decreased appetite, or the more difficult issues of constant nausea and vomiting.  Treatment with Reglan is intended to last for 4 to 12 weeks.  Many doctors are unaware of this recommendation, and end up prescribing Reglan for significantly longer periods.  This can have terrible consequences for the patient.
As with any medication, a detailed risk/benefit discussion with your doctor is critical.  Your prescribing medical professional must adequately explain the increased risk of tardive dyskinesia posed by use of Reglan, particularly with extended use.  Since Reglan is only intended to be used for short-term relief of gastrointestinal problems when other treatments have failed, the risks associated with long term use are very serious.  Failure to properly monitor the duration of use, or the over prescribing of the medicine, may be negligent on the part of the physician.

What is Tardive Dyskinesia (TD)?
Tardive dyskinesia is a neurological syndrome that can be caused by the long-term use of neuroleptic drugs, including Reglan.  Different classes of neuroleptic drugs are prescribed for psychiatric disorders, but Reglan also has neuroleptic characteristics.
Tardive dyskinesia is most often characterized by repetitive, involuntary, purposeless movements.  Patients suffering from TD may exhibit involuntary facial gestures, such as grimacing, tongue protrusion, lip smacking, puckering and pursing, and rapid eye blinking. They may also suffer rapid and involuntary movements of the fingers, hands, arms, shoulders, legs, and trunk.   TD can even adversely affect the ability to breathe, swallow, walk, and talk.  
Tardive dyskinesia is a serious and potentially irreversible disorder.  It can be caused by Reglan and metoclopramide.

What is the connection between Reglan and Tardive Dyskinesia (TD)?
The FDA and the pharmaceutical manufacturers have long recognized that Reglan increases the risk of tardive dyskinesia.  The physicians and the patients using the drug are rarely made aware of the true nature of the risk, and the label for the drug does a poor job of explaining the dangers.  Many physicians are unaware that the drug is intended for short term use only, and continue to prescribe Reglan month after month.
Scientific and medical studies have suggested that as many as 1 in 4 patients who take Reglan for more than a year may develop symptoms of TD.  The conditions can occur in much shorter time periods as well.  Both the amount and the duration of the prescription appear to increase the risk of developing TD.
Likewise, studies have shown that the risk of developing TD is greater for children (especially infants) than for adults taking Reglan.  While TD can afflict anyone taking Reglan, children are apparently much more susceptible to the effects of Reglan.
Often the diagnosis of TD is a difficult one to make.  Reglan actually conceals the very symptoms it is causing, which makes it a difficult diagnosis to make.  For this reason, symptoms of TD will often surface only after the drug is discontinued.  As a result, the true extent of the injury is often greater than anticipated, because Reglan is continuing to cause a greater injury, while hiding the symptoms.

How is Tardive Dyskinesia treated?
Unfortunately, there is no known treatment for tardive dyskinesia.  In some cases, the syndrome may resolve or the symptoms may be reduced weeks or even months after a patient stops taking Reglan.   For some patients, however,  the damage is irreversible.

What can you do?
Contact Class Action Lawyer Network for a Reglan Tardive Dyskenesia form Reglanlawyer