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Depakote Spina Bifida Lawsuit  
depakote spina bifida lawsuit

FDA Depakote Warning

Depakote (Valproate Sodium) and related products (valproic acid and divalproex sodium): Risk of Birth Defects

The FDA notified health care professionals and patients about the increased risk of neural tube defects, spina bifida and other major birth defects, such as craniofacial defects and cardiovascular malformations, in babies exposed to valproate sodium and related products (valproic acid and divalproex sodium) during pregnancy. Healthcare practitioners should inform women of childbearing potential about these risks, and consider alternative therapies, especially if using valproate to treat migraines or other conditions not usually considered life-threatening.

Women of childbearing potential should only use valproate if it is essential to manage their medical condition. Those who are not actively planning a pregnancy should use effective contraception, as birth defect risks are particularly high during the first trimester, before many women know they are pregnant. A valproate Medication Guide, provided with each outpatient prescription, will explain the benefits and risks of valproate and encourage patients to discuss options with their healthcare professional.[12/03/2009]

Depakote Side Effects to Unborn Infants

 

The most serious side effects of Depakote involve birth defects to the fetus. Many of the unborn children of these pregnant women taking Depakote are born with severe birth defects. These serious Depakote side effects may include:

  • Spina bifida
  • Skeletal defects
  • Intrauterine growth retardation
  • Neural tube malformations
  • Death of fetus
  • Craniofacial defects

Other Depakote Birth Defects Include:

  • Undescended testes
  • Hand structure malformations
  • Hypospadias (a urethra opening in the wrong place)
  • Pulmonary (lung) stenosis
  • Hypoplastic right heart

Depakote Lawsuits - Talk to a Depakote Attorney

 

If your child was born with severe birth defects, spina bifida or other skeletal or growth retardation it may have resulted from of Depakote being taken during pregnancy. Call and talk to Depakote Spina Bifida law firm that has represented thousands of clients over the last 25+ years and understands all aspects of drug litigation. Call for a Free & Confidential Depakote Spina Bifida Lawsuit Evaluation. Talk to a Board Certified Personal Injury Trial Lawyer licensed in Texas and in New York with a Nationwide Reputation.

 

Depakote Spinal Bifida & Neural Tube Defects - Free Case Evaluation.

(All Responses will Remain Confidential - Email or Phone Responses usually within 12-24 Hours)

Please fill out this form as completely as you can. Our law firm will call you back within 12-24 hours to discuss this matter with you.

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What City & State was the child born?
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Was Depakote taken during pregnancy?
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What has the child been diagnosed with?
Spina bifida
Skeletal defects
Intrauterine growth retardation
Neural tube malformations
Death of fetus
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NSF from MRI Gadolinium Contrast Dye in Kidney Failure, Dialysis Patients & Renal Failure  The FDA has reported a possible link between NSF/NFD, kidney failure and renal failure and the exposure to MRI dye / contrast called gadolinium. Patients with kidney disease, kidney failure, kidney or renal insufficeincy and kidney patients on kidney dialysis, may have contracted a horrible fibrosing skin disease from the gadolinium based contrast dyes used in MRIs. These MRI dyes have serious side effects which includes a rare skin, muscle & joint disorder called Nephrogenic Systemic Fibrosis (NSF). Patients with NSF often develop large areas of hardened skin with fibrotic nodules and plaques, reddened skin, muscle tightening, muscle weakness, joint pain and burning in joints along with itchy, thick areas of skin, usually on one's limbs. Click here for more information about Nephrogenic Systemic Fibrosis (NSF)  Recent reports link fractured femurs to the use of Fosamax. If you have fractured your leg or femur and have taken fosamx get a free case evaluation at www.fosamax-femur-fractures.com Fosamax Femur Fracture Lawsuits Fosamax Lawsuits Recent RFDA Depakote alert warns of Depakote use during pregnancy. Depakote may cause harm to the fetus resulting in spinal bifida, neural tube defects, growth retardation and other birth defects. For more information see depakote spina bifida  FDA warning Reglan may cause Tardive Dyskinesia (TD) a rare side effect of long time Reglan usage. Reglan has been linked to Tardive Dyskinesia. Tardive Dyskinesia is a central nervous system disorder characterized by involuntary movements of the limbs as well as twitching of the face and tongue similar to Parkinson's disease. See Metoclopramide and Tardive Dyskinesia TD for more information about reglan side effects. See Reglan Tardive Dyskinesia (TD) side effects lawsuits. Dilantin can cause SJS Stevens Johnson Syndrome and TENS. Get more info about Dilantin SJS Stevens Johnson Syndrome Lawsuit  Dilantin also can cause TEN (Toxic Epidermal Necrolysis) are more severe than others. Erythema multiforme minor is the milder form of SJS and not as serious as Erythema multiforme majoris. However, full blown Stevens-Johnson syndrone. If you or a loved one have taken Dilantin (phenytoin),Tegretol (carbamazepine), Lamictal (lamotrigue) or Levaquin (levofloxacin) and have been diagnosed with SJS or TENS or a loved one has died for complications of SJS Syndrome or TEN, Stevens-Johnson Syndrome (SJS) is a life-threatening condition affecting the skin in which cell death causes the epidermis (the outer layers of skin) separating from the dermis (inner layers of skin). See information about Stevens-Johnson Syndrome (SJS) Dilantin Lawsuit.Talk to a Dilantin SJS Dilantin Stevens Johnson Syndrome SJS Dilantin TEN lawyer about Dilantin TEN Toxic Epidermal Necrolysis Diagosis and your legal rights to a Dilantin lawsuit .Byetta Pancreatitis Lawsuits Toyota Gas Pedal Recall News

 

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