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TAKE CONTROL TODAYMost side effects from taking Depakote go away with no lasting harm. But a few people have serious reactions that can even be life-threatening.
Here's a list of symptoms that may be the start of one of these problems. If you notice any of these symptoms, call the doctor immediately:
The best-known and most feared serious reaction is liver damage, which has been fatal for some people. This damage usually occurs within the first 6 months of treatment. The risk of liver failure is much higher in children under 2 years of age, especially if they:
The risk of liver failure is much lower in children between 2 and 10 and is very low in older children and adults, perhaps 1 in 50,000. This is similar to the frequency of liver failure when taking other seizure medicines, such as Dilantin (phenytoin). There is no evidence that long-term use of Depakote will cause gradual, progressive damage to the liver.
Another rare but potentially life-threatening reaction to Depakote is pancreatitis (inflammation of the pancreas), which occasionally progresses to bleeding and death. This reaction may occur in both children and adults, even after several years of taking Depakote. Report pain in the abdomen, upset stomach, vomiting, or loss of appetite to the doctor right away.
Problems with blood clotting are more likely when high doses of Depakote are taken. Sometimes these problems return to normal without stopping the Depakote. The doctor probably will order some blood tests before starting treatment with Depakote, and will repeat them some time later and before any elective surgery.
A complete list of all reactions to Depakote can be found in the package insert, but it is important to remember that only a tiny number of people have any of these serious problems.
On July 10, 2008, an advisory panel was convened by the Food and Drug Administration (FDA) to review data that the FDA had previously collected from drug studies showing an association between many of the antiepileptic drugs (AEDs) and suicidal ideation and behavior, which together are called suicidality. According to the FDA’s Alert, among the patients with epilepsy in these drug studies, 1 out of 1000 people taking the placebo (inactive substance) showed suicidality compared to approximately 3.5 out of 1000 people who took an AED. The FDA advisory panel voted to accept the FDA's data at its meeting on July 10. The FDA has provided the following information for patients, family members, and caregivers at www.fda.gov/cder/drug/InfoSheets/HCP/antiepilepticsHCP.htm.
We again urge patients and families to contact their doctor before stopping an epilepsy medication because this may possibly lead to seizures and worsening of mood.
Reviewed July 2008 by Steven C. Schachter, MD, epilepsy.com Editorial Board.
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