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Lamotrigine-induced carbamazepine toxicity: an interaction with carbamazepine-10,11 -epoxide

โœ Scribed by T. Warner; P.N. Patsalos; M. Prevett; A.A. Elyas; J.S. Duncan


Book ID
103932280
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
381 KB
Volume
11
Category
Article
ISSN
0920-1211

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โœฆ Synopsis


We report an interaction between lamotrigine (LTG), a new antiepileptic drug (AED), and carbamazepine (CBZ) and its primary metabolite CBZ-10,11-epoxide (CBZ-E) in 9 consecutive patients (5 male, 4 female, aged 19-31 years). After introduction of LTG (median daily dose 200 mg, range 100-300 mg) the mean serum CBZ-E concentration increased by 45% (P less than 0.01) and the CBZ-E/CBZ ratio increased by 19% (P less than 0.02). In 4 patients these changes were associated with clinical toxicity (dizziness, nausea, diplopia). The possibility of an increase in serum CBZ-E concentrations needs to be considered if toxicity symptoms develop when LTG is added to CBZ therapy.


๐Ÿ“œ SIMILAR VOLUMES


In vivobinding characteristics of carbam
โœ Y. Kodama; K. Tsutsumi; M. Kuranari; H. Kodama; I. Fujii; M. Takeyama ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Springer ๐ŸŒ English โš– 292 KB

The in vivo serum protein binding characteristics of carbamazepine (CBZ) and carbamazepine-10,11-epoxide (CBZ-E) were assessed in sera from 23 paediatric patients on CBZ monotherapy. We assumed that CBZ and CBZ-E binding to serum proteins comprised specific binding sites on alpha 1-acid glycoprotein