2003
DOI: 10.2165/00044011-200323100-00006
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Oxcarbazepine versus Divalproex Sodium for the Continuing Treatment of Mania

Abstract: Oxcarbazepine showed comparable efficacy to divalproex sodium, yet appeared to do so with an equal or more benign side-effect profile, particularly with regard to weight. These results suggest that oxcarbazepine, which has been used in Europe for the treatment of mood disorders for some time (albeit used off-label for this purpose) may show promise for use in the US as an agent for maintenance of non-acute mania.

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Cited by 11 publications
(20 citation statements)
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“…Unlike CBZ, OXC is not metabolized by oxidation, thus circumventing the generation of the 10,11-epoxide species thought to be responsible for much of the toxicity of CBZ. There is no established therapeutic window for OXC in contrast to CBZ; therefore, monitoring plasma concentration may only be useful in cases of intoxication [1,2,[4][5][6].…”
Section: Pharmacology Of Oxcarbazepinementioning
confidence: 99%
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“…Unlike CBZ, OXC is not metabolized by oxidation, thus circumventing the generation of the 10,11-epoxide species thought to be responsible for much of the toxicity of CBZ. There is no established therapeutic window for OXC in contrast to CBZ; therefore, monitoring plasma concentration may only be useful in cases of intoxication [1,2,[4][5][6].…”
Section: Pharmacology Of Oxcarbazepinementioning
confidence: 99%
“…10 Bipolar depression and schizoaffective 6-16 months Randomized study of OXC (n = 4) vs lithium (n = 6) Adjunct (n = 3) and monotherapy 2/4 (50%) with no relapses on OXC vs 3/6 (50%) with no relapses on lithium [23] Wildgrube Unknown Lithium response (67%) greater than OXC response (33%) [42] Teitelnaum [2] Ghaemi et al [20] Schaffer et al [15] Comes et al…”
Section: Monotherapymentioning
confidence: 99%
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