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Wellbutrin is commonly prescribed to women who are or may become pregnant for several reasons, including as an antidepressant SSRI aid and as a smoking cessation pill. Regardless of the reason, women who take this drug may experience a greater than average risk of infant child birth defects, including but not limited to heart defects, cleft palate, cleft lip, skeletal deformations and more. If your child experienced such a horrific side effect, please call us today for a free case evaluation on how we can help.

Wellbutrin Information

Our team of Wellbutrin lawyers would like to report on some general information about Wellbutrin, and if you or your loved one has given birth to a child with a birth defect, including a heart defect, and you took Wellbutrin during pregnancy, we would be honored to discuss your situation.

Consumption of Wellbutrin during pregnancy can result in the baby being born with Down’s syndrome. Some babies may be born with Spina bifida.

Down’s syndrome 

Down’s syndrome is a genetic defect that is apparent at birth. The baby is somewhat floppy, and there are characteristic features of the face and hands. Down’s syndrome children are usually easy to manage as infants. They are often rather placid. Development will be delayed once the child is old enough to walk and talk. A Down’s syndrome child will qualify for various programs for handicapped babies and other services from the time he or she is born. Special school will probably begin at three years of age. Some Down’s syndrome children can function in elementary school in a regular classroom. Most do not, and are placed in a special education setting.

Congenital heart disease 

Some Down’s syndrome children have congenital heart disease and need surgery to correct it. Some defects are quite severe and some are actually fatal. Many of these children need glasses and some are visually impaired, even with glasses. Having the child’s eyes tested may be difficult for younger children, because they cannot cooperate with the testing. Hearing may also be abnormal.

Raising a Down’s syndrome child 

Raising a Down’s syndrome child is difficult for any parent, but it is especially challenging for a substitute parent. At any age, the child will not be able to tell you much about his history and will not be able to understand the details of what you are trying to ask or tell him. It will require extra patience to work with this child, but the rewards are great. Most Down’s syndrome people are friendly and calm and pleasant family members. School will generally continue past the age of eighteen. Planning for this child, as he becomes an adult, will be very important.

Spina bifida 

Spina bifida, a birth defect of uncertain origin, serves as an example. The spinous process, a portion of the vertebrae, is split in children with spina bifida and part of the spinal cord is malformed and may be extruded either into a blisterlike bag or outside it, if the bag has ruptured; hydrocephalus is common. Most frequently, such children are paralyzed and suffer from bladder and bowel infections, malfunction, or incontinence. It is not unusual for them to be mentally retarded. In the past, most spina bifida children died from meningitis after a short life because of the spinal cord’s continual exposure to infection. Today, however, medical technology can sustain the life of many children who previously would have died. Modern techniques include straightening the spine, closing the lesion, draining the hydrocephalus if one has developed, and eliminating infection through medical treatment. The result is that a large percentage of the children having spina bifida survive, but a large number of them are physically handicapped and mentally retarded.

If you would like more information in Wellbutrin claims for birth defects, please continue reading.

The Problem

Our firm is offering free nationwide case evaluations to families whose children were diagnosed with medical conditions at birth or shortly therafter when the mother ingested Wellbutrin or Bupropion during pregnancy. Specific birth defects include cardiac malformations (ASD, VSD, Left Hypoplastic Heart Syndrome, coarctation of the aorta, Tricuspid or Pulmonary Atresia, Pulmonary Stenosis, transposition of the great vessels or any other heart defect), neural tube defect, craniosynostosis, cleft lip, cleft palate, skeletal deformations, and club foot.

About Wellbutrin

Wellbutrin is an antidepressant drug prescribed to treat major depressive disorder, also called major depression and clinical depression, and seasonal affective disorder, a type of depression involving adverse side effects that occur each year during the same season. First approved by the FDA in 1985, bupropion hydrochloride was available for several years only under the brand name Wellbutrin. In 1996, the FDA approved a sustained-release tablet of this drug called Wellbutrin SR and, in 2003, approved an extended-release tablet known as Wellbutrin XL.

Wellbutrin carries a Pregnancy Category C classification, meaning that animal reproduction studies have shown an adverse effect on the fetus but that no adequate or well-controlled studies in humans have been performed.

Wellbutrin has been linked to congenital heart defects. Congenital heart defects affect approximately 40,000 babies each year, and one of the primary known causes of such birth defects is the ingestion of teratogenic drugs during pregnancy. A teratogen is a drug or other substance capable of interfering with the development of a fetus that can ultimately result in serious birth defects.

Alleged Birth Defects

Anti-depressants have become a troubling subject when it comes to teenagers; however, some mothers are unfortunately giving birth to children with birth defects that may be connected to taking drugs called Selective Serotonin Reuptake Inhibiters (SSRIs) during early pregnancy.

SSRI birth defects, which include heart problems, spina bifida, club foot, cleft pallet, and others, are causing concerning and leading to litigation filed against the makers of these dangerous drugs.

Complaints of SSRI birth defects have been identified since at least 2005 from women who ingested during early pregnancy, Zoloft, Celexa, Lexapro, Paxil, Prozac, and Wellbutrin while pregnant. SSRI drugs are generally used as anti-depressants or to stop smoking.

A New England Journal of Medicine study found that women who took SSRIs during third trimester were six times more likely to deliver babies born with primary pulmonary hypertension (PPHN) than those who did not take the SSRIs during their third trimester.  PPHN is a lung disorder that restricts the arteries and causes blood pressure in the pulmonary artery of the heart to rise beyond control.

Symptoms of PPHN may include the following:  heart murmurs, rapid heart rate, bluish skin, low blood oxygen levels, difficulty breathing diagnosing PPHN.

PPHN is a serious birth defect.  Even after treatment, infants can be susceptible to heart failure, brain hemorrhage, seizures, kidney failure or organ damage.  Some of these birth defects can be present throughout life or even fatal.  Some infants who happen to survive PPHN nevertheless have long term breathing difficulties, seizures, developmental delays and hearing loss.

Zoloft, Celexa, Lexapro, Paxil, Prozac, Wellbutrin and Zyban are anti-depressants or smoking sensation drugs that have fallen under close scrutiny for use by expectant mothers.  As consumers of prescriptions drugs, our society assumes that pharmaceutical companies test for the safety as well as the effectiveness of prescription medication.  Unfortunately, there are and have been several drugs on the market that can cause injury, illness or even death.  In these cases, the negligence of a pharmaceutical company may warrant a personal injury lawsuit.

Such a condition may cause surgery, lifetime defects or death.

Getting Legal Help

If your child is born with a birth defect and you had been prescribed Wellbutrin during pregnancy, you may have a claim for compensation. You may be eligible for compensation for the medical expenses for the treatment of your child and also compensation for your mental sufferings.

If you or a loved one took Wellbutrin during early pregnancy and had a child born with a birth defect, this side effect may be associated with Wellbutrin. Members of our firm are currently reviewing potential Wellbutrin lawsuits. If you have a question or have suffered serious side effects, a Wellbutrin lawyer can be reached by email or by calling TOLL FREE 1-800-632-1404.

Members of our firm are attorneys currently representing clients who have taken several prescription drugs and claim injuries associated with those drugs, includingTopamax®, Wellbutrin®, Fosamax®, and Actos®. They and members of the firm also represent clients across the globe pertaining to medical device failures, including theAdvanced Bionics HiRes90k® cochlear implant , the TVM / TVT transvaginal mesh – sling and the DePuy hip implant. For a free case evaluation, please contact:

TOLL FREE: 1-800-632-1404

EMAIL: click here

FILL OUT THIS FORM:

NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.

FREE NATIONWIDE CASE EVALUATIONS: CALL 1-800-632-1404

Our team of attorneys are now investigating claims and prepared to file Mirena lawsuitsinvolving the intrauterine contraceptive device Mirena®. Manufactured by Bayer Healthcare Pharmaceuticals, Inc., Mirena is an IUD device [intrauterine device] that must be inserted by a trained health care provider and is intended to provide contraceptive protection for up to five years. Some women have experienced serious adverse side-effects and potentially life-threatening complications following the implantation of theMirena device, including perforation of or imbedment in the uterus.

Mirena Injuries

Mirena is alleged to have many side effects. Mirena is an interuterine contraceptive device {IUD}. As a Mirena attorney that wants to provide information to women or their loved ones about making a Mirena claim or to discuss a Mirena lawsuit, Mirena has its own side effects. One such side effect is perforation of the cervix.

Mirena has a small amount of synthetic progesterone hormone that goes into the wall of the uterus. Women who use the Mirena device have lighter, less painful menstrual periods. Some women may have light, irregular bleeding or spotting throughout the cycle. Others have no menstrual periods at all. A few women have mood changes, less enjoyment of sex, or headaches due to the hormones in Mirena, but this is not common.

Uterine Perforation

Another side effect of using the Mirena device is uterine perforation. The main dangers of such uterine perforation include bleeding and trauma to the abdominal viscera as well as damage to internal organs such as bowel, omentum, mesentery, ureter and fallopian tube.

Fertilization

The fallopian tubes are an integral part of the reproductive system. It plays an important part in the woman becoming pregnant. She must have at least one functioning fallopian tube. Typically she will ovulate every twenty-eight days or so, and this will take place towards the middle of the cycle when the mature egg will be released from the follicle on either her right or left ovary. The fallopian tube will pick up the egg which will start a slow journey down it. Within twenty-four hours of release, the egg will be positioned ready to receive sperm. After sex, sperm are normally deposited at the cervix in hundreds of millions. The sperm that arrive at the ampulla, the site of fertilisation, must have undergone an epic journey through the cervical mucus, across the uterus and through the fallopian tube. Once the sperm finds the egg, it will penetrate the egg. Fertilisation has occurred and the fertilised egg, now described as an embryo, will begin to grow. Within forty-eight hours, the embryo will have divided twice to form a four-cell embryo. At this stage the embryo is still located in the fallopian tube.

Infertility

Any damages to or defect in the fallopian tubes can cause infertility in the woman. Women use the Mirena device as a contraceptive to prevent pregnancy but they can remove the device if they intend to get pregnant. However if the Mirena device has perforated the uterus and the uterine perforation has caused damage to the fallopian tubes, then the woman suffer from infertility and will have problems getting pregnant.

To learn more about Mirena or its side effects, pleast continue reading.

Side Effects

Some women who have had Mirena implanted experienced serious and even debilitating or life-threatening side-effects. The device may migrate from its original position after being inserted, perforating the uterus or embedding itself in the uterus. In both instances, a doctor must locate and surgically remove the device. Mirena may also migrate outside the uterine cavity and cause adhesions or scarring that can lead to infertility. Depending on the damage caused, affected women may require a complete hysterectomy, and more serious complications could result in death.

Serious side effects that have been linked to Mirena include:

• - Abscesses
• - Embedment in the uterus
• - Erosion of adjacent areas such as the vagina
• - Infertility
• - Inflammation of the membrane that lines the abdominal cavity and internal organs (Peritonitis)
• - Intestinal perforations or obstruction
• - Pelvic Inflammatory Disease
• - Perforation of the uterus

If you experienced adverse Mirena side effects, required surgery or have a loved one who suffered death following the implantation of Mirena, you may have a potentialMirena lawsuit.

No Recovery, No Fee

We take Mirena litigation cases on a contingency basis. That means that there is no cost to you unless we and our co-counsel are able to recover a settlement or judgment on your behalf. So, unless your case is resolved by trial, arbitration, settlement, or other resolution, you do not have to pay any attorney fees to us, or pay any costs. Litigation costs include filing fees, court reporter fees for deposition, copying costs, experts, and travel. Litigation costs are paid by our firm so you don’t have to have cash to pursue justice against medical device corporations.

About us

Our team of attorneys have been retained by clients across the country as to allegedly defective and improperly designed Mirena devices.  In fact, our team of attorneys has represented patients around the globe for the allegedly defective Advanced Bionics HiRes90k cochlear implant device and other medical devices including the DePuy hip implant and the transvaginal mesh and transvaginal sling devices.

As a Mirena attorney, we will investigate your claim and with our co-counsel we stand ready to push your case ahead.

FOR A FREE CASE EVALUATION:

CALL TOLL FREE: (800) 632-1404

EMAIL: clicking here.

FILL OUT THIS FORM FOR FREE HELP:

NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.

FREE CASE EVALUATION: 1-800-632-1404

Tens of thousands of women receive a transvaginal mesh (TVM) device each and every year from numerous suppliers: American Medical Systems, Bard, Boston Scientific, Ethicon,Gynecare, and Johnson & Johnson.  Thousands of women have been injured through no fault of their own, including vaginal erosion, pain, urinary problems, bleeding, infection and more. Our attorneys are representing women in all fifty states and Canada who have been injured.  For a free case evaluation, call 1-800-632-1404.

Women Experience Pain

From a medical standpoint, when pain occurs following the implantation of a transvaginal mesh (TVM) device, it is generally secondary to the mesh being placed too tight or healing in a position that is pulling on the muscles and nerves that are causing irritation. It can also occur if the mesh is not lying properly. In these situations, sexual intercourse becomes painful and uncomfortable. Life also becomes difficult.

When this occurs, many physicians will employ a conservative approach. Conservative therapy includes pelvic floor physical therapy (manual therapy on the muscles and nerves in the vagina to help relax and/or relieve spasms that may be causing pain). Some women have described temporary relief having undergone physical therapy for this, but find that the problem simply recurs once there therapy ends.

Another option are trigger point injections (TPIs).  Trigger point injections into the muscles or nerves in the vagina that may be causing the pain is another approach. If the pain persists and doesn’t respond, surgery may be necessary.

In severe cases an abdominal approach will be necessary to take care of pain. If this is the case, most surgeons recommend major surgery with a large abdominal incision. This can obviously be extremely painful to the patient, and cause life-disrupting complications. It is important to note that with any pelvic surgery, pain can be a complication whether mesh is used or not.

Our team of attorneys is reviewing case evaluations for women across the country who have received TVM and TVT products from manufactures such as C.R. Bard, Avaulta, Boston Scientific, and Johnson & Johnson’s Ethicon.

If you need help from a transvaginal mesh device injury, call us today for help.

 The Problem

In 2008, the FDA first released concerns about the safety of transvaginal placement of mesh. From 2008 to 2010, the FDA received three to five times as many adverse reports associated with mesh used for pelvic organ prolapse repair than what agency received from 2005 to 2007 (nearly 1,000 reports of adverse events were received from 2005-2007).

Many of these patients complain because of erosion or contraction of the mesh material (which has been described as being of a similar material as Rubbermaid storage containers).  The erosion leads to bleeding, severe pelvic pain, painful (or impossible) sexual performance and a recurrence of urinary problems.

In July 2011, the Food and Drug Administration (FDA) issued an update related to what it called ‘serious complications’ related to the use of vaginal mesh for treatment of pelvic organ prolapse (POP) and stress urinary incontinence (SUI).  It is now known that complications linked to transvaginal placement of surgical mesh in SUI and POP patients are not rare and can require multiple surgeries to correct problems related to the use of surgical mesh. In fact, the FDA now says that additional surgeries may actually not be able to repair damage caused by implantation of the mesh.

In other words, the side effects of the mesh placement may be permanent.  These complications from transvaginal placement of surgical mesh include:

• -Erosion of the implanted mesh
• -Infection and/or bleeding
• -Pain, including pain during sexual intercourse
• -Problems with organs near the implantation site

Helping You

You may have experienced mesh erosion, bleeding, urinary infections, vaginal scarring, pain during sexual intercourse, failure to conduct sexual intercourse and more. A physician may have tried to remove the mesh and been unable to do so. You may be in excruciating pain, and need help. We are offering free case evaluations to the general public across the United States and Canada. Manufacturers we consider include American Medical Systems, Bard, Boston Scientific, Ethicon,Gynecare, and Johnson & Johnson.

If you received a transvaginal mesh / sling and have been injured, you may be entitled to monetary compensation. Problems include pain, inability to have intercourse,bleeding, mesh growth into the body, mesh erosion, and more. Problems could be irreversible. Please fill out the form to the right or call us so that we can provide you with forms to evaluate your potential case immediately.

We are accepting case evaluations nationwide and in Canada, as well.  Please do not hesitate or delay in contacating TVM / TVT Sling and transvaginal mesh attorneys :

CALL: 1-800-632-1404

EMAIL: clicking here

FILL OUT THIS FORM FOR A FREE CONSULTATION AND CASE EVALUATION:

NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.

FREE CASE EVALUATION: 1-800-632-1404

Topamax can cause birth defects, including cleft palate, cleft lip, and genital and skeletal deformities. Please contact us immediately for a free consultation on a Topamax birth defect. We are standing by now to explain to you questions about Topamax lawsuits, Topamax class action lawsuits, Topamax injuries and Topamax side effects.

Following the FDA’s new safety announcement concerning the link between Topamax and oral cleft birth defects, the Consumer Justice Foundation developed an educational resource to provide mothers with more information about Topamax birth defects. According to this recent FDA action, there is an increased risk of oral clefts like cleft lip and cleft palate among infants whose mothers take Topamax while pregnant (fda.gov). After reviewing new Topamax birth defect data, the FDA has also elevated the pregnancy category of Topamax from C to D, which means there is positive human evidence of the drug’s potential to cause serious harm to a fetus when taken during pregnancy (fda.gov).

Topamax is a prescription anticonvulsant drug, currently manufactured by Ortho-McNeil Pharmaceutical, a division of pharmaceutical giant Johnson & Johnson. Although anticonvulsant drugs were originally designed to treat epilepsy specifically, many of these medications have been indicated for additional purposes in recent years. The FDA approved Topamax, for example, in 1996 for the treatment of epilepsy, and again in 2004 for the prevention of migraine headaches. Since its introduction to the U.S. market, Topamax has become one of the most commonly prescribed anticonvulsants available.

Cleft lip and cleft palate occur when a child’s oral structures fail to develop properly in utero. Cleft lip is characterized by a vertical fissure in the upper lip which may extend up through the nose. Cleft palate can vary in severity from a small opening at the back of the mouth to a nearly complete separation of the roof of the mouth. Children born with cleft lip or cleft palate may struggle with severe side effects like feeding difficulties, recurring ear infections, dental problems, hearing loss, and delays in speech and language development.

If your child was born with cleft lip, cleft palate or any other birth defect after you took Topamax when pregnant, do not delay in calling us for help.

Ed Wallis is an attorney currently representing and seeking clients who have taken several prescription drugs and claim injuries associated with those drugs, including Wellbutrin, Paxil, Topamax, Avandia, Accutane and Reglan. He also represents clients across the globe pertaining to medical device failures, including the Advanced Bionics HiRes90k cochlear implant, the Gynecare Prolift transvaginal mesh – sling and the DePuy hip implant. In fact, Mr. Wallis and others in the firm in which he practices serve as counsel to persons around the world for defective medical devices and drugs.

For a free case evaluation and to immediately discuss the facts of your potential claim, please contact us before your time to act runs out:

CALL: (901) 527-2125

TOLL FREE: 1-800-632-1404

EMAIL: click here

FILL OUT THIS FORM:

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The Hill (9/2, Pecquet) reports, “Forbes magazine this week released its first-ever survey of America’s most profitable hospitals, revealing that 24 hospitals with more than 200 beds make 25 cents or more for every dollar of patient revenue they take in. The report is being widely disseminated by the health insurance industry, which is pushing back against claims that health insurance profits — rather than rising medical costs — are to blame for rising premiums.” In the survey, “Forbes points out that hospital charges account for about a third of healthcare spending, or $718 billion — more than any other single category.” In an earlier report, Bloomberg cited Princeton economist Alain Enthoven saying that hospital expenses rose “largely because of the pricing power of local hospital systems,” and calling for “effective antitrust enforcement.”

If you or a loved one in Tennessee, Mississippi or Arkansas believes you are the victim of medical malpractice and have sustained an injury to yourself or your child, infant, parent or loved one, including because of failure to diagnose a medical condition, please call us today for a free case evaluation:(901) 527-2125.

Attorneys Tim Edwards and Ed Wallis practice medical malpractice law in Memphis, Tennessee and throughout West Tennessee and the Mid South area, including Eastern Arkansas, Northern Mississippi and West Tennessee. Mr. Edwards and Mr. Wallis are prepared to discuss the facts of your Memphis medical malpractice case case and try and determine if there is a way to help you. We are committed to a personal relationship with our clients. When you retain us to help you, you will have our cell phone numbers and direct numbers to our desks so that we can be reached when you need us.

Medical malpractice is a complex area of the law, and you should immediately contact an attorney willing to provide detailed and thorough review of your case for you. Do not be fooled by the gimics of a quick check from a television ad; for a medical malpractice case, Advanced Bionics cochlear implant recall case, a Transvaginal Mesh case, or a laser eye surgery case, you need a serious attorney who will work seriously on your behalf.

Mr. Edwards and Mr. Wallis accept clients on a natiowide basis for the prescription drugs Wellbutrin, Accutane, Reglan, Levaquin, Januvia, and Yaz. Mr. Wallis and Mr. Edwards ar representing clients internationally for the Advanced Bionics cochlear implant, and nationally on Gynecare prolift transvaginal mesh, tape, sling device.

For immediate help:

CALL: (901) 527-2125

AFTER HOURS: (901) 275-0600

EMAIL: Tim or Ed by clicking here.

FILL OUT THIS FORM FOR FREE HELP:

Lawsuits have been filed on behalf of those injured after taking the drug Reglan. While the lawsuits contain many pages and are crafted to deal with the particulars of each particular plaintiff, the following still show the pathetic conduct of the pharmaceutical giant, if the allegations are found to be true:

• Wyeth knowingly, intentionally and negligently disseminated misleading information
  to physicians’ across the country, through a publication known as the Physicians’
  Desk Reference, labeling information for Reglan, metoclopramide and metoclopramide
  HCl which mislead the medical community, physicians and Plaintiff’s physician
  about the risks of long term ingestion of the drug.
• Wyeth knowingly, intentionally and negligently disseminated misleading information
  to physicians’ across the country, through a publication known as the Physicians’
  Desk Reference, labeling information for Reglan, metoclopramide and metoclopramide
  HCl which mislead the medical community, physicians and Plaintiff’s physician
  about the increased risk of extrapyramidial side effects, including tardive
  dystonia, diabetics were exposed to.
• Wyeth, Schwarz and Pliva had access to and knew that severe side effects would
  result from the use of Reglan/ metoclopramide in the manner in which physicians
  were prescribing Reglan, metoclopramide HCl and/or metoclopramide and the fact
  that physicians did not fully understand the risks associated with Reglan,
  metoclopramide HCl and/or metoclopramide through the defendants participation,
  individually and jointly, in or its ability to review data from clinical studies
  that were not publicly available, through its review of domestic and international
  medical literature concerning Reglan/ metoclopramide and through ongoing
  litigation.
• Wyeth failed to adequately warn physicians about the risks associated with Reglan,
  metoclopramide HCl and/or metoclopramide despite the fact that Wyeth knew that
  physicians, the medical community, the generic pharmaceutical industry, Plaintiff
  and other similarly situated relied on Wyeth to disclose what it knew and what it
  should have known from a prudent review of the information that it possessed or to
  which it had access.
• Defendant Wyeth knew, or should have known through the exercise of reasonable
  care, that the package insert for Reglan, metoclopramide HCl and/or metoclopramide
  substantially understated the prevalence of acute and long term side effects of
  Reglan, metoclopramide HCl and/or metoclopramide. Wyeth failed to use reasonable
  care to modify the package insert to adequately warn physicians about the true
  risks of both short term use and long term use, even after several injured
  patients filed lawsuits alleging inadequate warnings and produced competent expert
  testimony supporting their allegations.

Do not stop taking Reglan without talking with a physician, but contact us today for a free case evaluation if you have tremmors, shakes or been disagnosed with tardive dyskinesia. We may be able to help.

Metoclopramide is available in a several forms and the names include some version of Reglan or the actual word, metoclopramide. More than 2 million people in this country are taking some form of the drug, according to FDA estimates. Reglan manufacturers including Wyeth, a successor-in-interest to A.H. Robins, Inc., and American Home Products Corporation, and Schwarz Pharma, Inc. Generic manufacturers of metoclopramide including Teva Pharmaceuticals and Actavis Elizabeth.

If you have been injured…

DO NOT DELAY. YOUR ABILITY TO RECOVER MONETARY COMPENSATION MAY BE LIMITED BY STATE LAW. CALL ED WALLIS OR FILL OUT THE FORM BELOW FOR A FREE CASE EVALUATION:

CALL: (901) 527-2125

AFTER HOURS: (901) 275-0600

EMAIL: Tim or Ed by clicking here.

FILL OUT THIS FORM FOR FREE HELP:

Other Materials to Read:

Tennessee Reglan Lawyers To Provide Free Case Evaluations

Food and Drug Administration (FDA) video on Reglan Warning, potential lawsuit help and free case evaluation

Reglan Attorneys in Tennessee

Tennessee: Help for Reglan Injuries

Reglan litigation page

Attorneys Tim Edwards and Ed Wallis of the firm Glassman, Edwards, Wade & Wyatt have filed two lawsuits in Los Angeles Superior Court on behalf of their injured clients surrounding the twice recalled Advanced Bionics HiRes90k cochlear implant. The lawsuits filed allege wrongdoing by the cochlear implant manufacturer for the manufacture and sale of the device, which has been marketed as the most reliable cochlear implant in the world.

The two lawsuits were filed on behalf of injured adults in Iowa and Kentucky. To contact Mr. Edwards or Mr. Wallis about a potential case and a free case evaluation, please call (901) 527-2125.

For a free copy of the lawsuits filed, please fill out this form:

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Expect lawsuits against mortgage lenders to begin rolling in over the next year.

Read more HERE.