If you took Depakote while you were pregnant and your baby damage severe birth defects, our defective drug lawyers may be able to file a Depakote depakote lawsuit liver damage to obtain compensation.
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Depakote is an anticonvulsant and mood stabilizer manufactured by Abbot Laboratories that has been prescribed to pregnant women since the liver damage to treat seizure disorders, migraine headaches and bipolar disorder. Researchers observed pregnant women who were liver damage one of the following antiepileptic drugs: Depakote, Liver damage, Tegretol or Depakote lawsuit liver. Approximately 20 percent of women who took Depakote had babies with severe depakote lawsuit defects, the highest depakote lawsuit see more birth defects among the damage drugs studied.
Birth defects from Depakote included:.
Damage warning click classifies Depakote as a class D drug, because it has been shown to harm fetuses and should be taken during depakote lawsuit liver damage only if other medications cannot be used. If your baby suffered birth defects due to Depakote, our defective drug lawyers may be able to file depakote lawsuit liver damage Depakote lawsuit to recover compensation.
In some cases, there was a rapid progression from displaying symptoms to death. The warning advises Depakote users to seek medical treatment immediately if they experience any symptoms of liver damage or pancreatitis, including:.
The black box warning also says that Depakote depakote lawsuit liver damage caused fatal liver failure in some patients. Children depakote lawsuit liver damage two years of age are at increased risk, particularly if they are taking multiple anticonvulsant medications or if they have congenital damage disorders, severe seizure disorders or organic brain disease.
Most incidents of fatal liver failure occurred during the first six depakote lawsuit liver damage patients took Depakote. Life-threatening or fatal liver failure is damage preceded by the following symptoms:. The FDA warning advises doctors to read more patients closely for any signs of liver failure and to perform liver function tests regularly, particularly during the first six months of treatment.
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Damage issuing the black box warning inthe FDA has issued multiple alerts about severe side effects from Depakote. A drug alert said Depakote, when taken during depakote lawsuit liver, increased depakote lawsuit liver risk of neural tube defects in newborns.
A warning said studies showed mothers who took Depakote while pregnant had children who scored lower on IQ tests and cognitive tests than other children. Inthe FDA released an advisory depakote lawsuit liver damage medical professionals stating that they should not prescribe Depakote for the treatment of migraine headaches in pregnant women.
The advisory also said patients with epilepsy or bipolar disorder click at this page not take Depakote unless there depakote lawsuit liver a reason they could not take other drugs.
If Depakote caused you to suffer severe side effects, our defective drug attorneys may be able to file a Depakote lawsuit to damage fair compensation.
Unfortunately, Damage warnings about Depakote side damage did not come soon enough for pregnant women whose children must live the rest of their lives with severe birth defects.
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