A Review of Eslicarbazepine Acetate for the Adjunctive Treatment of Partial-Onset Epilepsy
Author(s) -
Rajinder Singh,
Jorge J. Asconapé
Publication year - 2011
Publication title -
journal of central nervous system disease
Language(s) - English
Resource type - Journals
ISSN - 1179-5735
DOI - 10.4137/jcnsd.s4888
Subject(s) - oxcarbazepine , carbamazepine , medicine , somnolence , nausea , hyponatremia , epilepsy , lacosamide , placebo , pharmacology , vomiting , drug , adjunctive treatment , anesthesia , adverse effect , psychiatry , alternative medicine , pathology
Eslicarbazepine acetate (ESL) is a novel antiepileptic drug indicated for the treatment of partial-onset seizures. Structurally, it belongs to the dibenzazepine family and is closely related to carbamazepine and oxcarbazepine. Its main mechanism of action is by blocking the voltage-gated sodium channel. ESL is a pro-drug that is rapidly metabolized almost exclusively into S-licarbazepine, the biologically active drug. It has a favorable pharmacokinetic and drug-drug interaction profile. However, it may induce the metabolism of oral contraceptives and should be used with caution in females of child-bearing age. In the pre-marketing placebo-controlled clinical trials ESL has proven effective as adjunctive therapy in adult patients with refractory of partial-onset seizures. Best results were observed on a single daily dose between 800 and 1200 mg. In general, ESL was well tolerated, with most common dose-related side effects including dizziness, somnolence, headache, nausea and vomiting. Hyponatremia has been observed (0.6%-1.3%), but the incidence appears to be lower than with the use of oxcarbazepine. There is very limited information on the use of ESL in children or as monotherapy.
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