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TAKE CONTROL TODAYVery few people have serious reactions to oxcarbazepine. If you take it, you should be aware of them, however, so you and your family can recognize them.
Here's a list of warning signs that may possibly be the start of a serious problem. If you notice any of these things, call your doctor right away:
Severe Skin Reactions
As of April 19, 2005 the FDA and Novartis pharmaceuticals (the manufacturer of the brand name version of oxcarbazepine called Trileptal) issued a new warning regarding oxcarbazepine. Serious dermatological reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported in both children and adults in association with oxcarbazepine use. SJS and TEN may start with fever and flu-like symptoms. Then, a rash develops, with or without ulcers of the mucous membranes, that quickly progresses to blisters that burn and are painful.
The most common time of onset after first dosage of oxcarbazepine was 19 days. Such serious skin reactions may be life-threatening, and some patients have required hospitalization with very rare reports of fatal outcome. Therefore, if you have any skin reactions upon taking oxcarbazepine, you should seek immediate medical attention.
Hyponatremia
The last five items in this list could occur if you have a low level of sodium (salt) in your blood, a condition called hyponatremia. This condition has been reported in about 1 in every 40 patients taking oxcarbazepine. It has occurred most often during the first 3 months of treatment, but in some cases it has been discovered much later. Usually it is not serious. You might even have it without noticing anything wrong. But now and then it does cause major problems, so your doctor may want to check the sodium level in your blood to see if this is happening to you.
It is important to remember that only a tiny number of people who take oxcarbazepine have any 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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