Pharmacokinetic and pharmacodynamic interaction of lorazepam and valproic acid in relation to UGT2B7 genetic polymorphism in healthy subjects.

@article{Chung2008PharmacokineticAP,
  title={Pharmacokinetic and pharmacodynamic interaction of lorazepam and valproic acid in relation to UGT2B7 genetic polymorphism in healthy subjects.},
  author={J L Chung and J-Y Cho and K-S Yu and J. H. Kim and Kyoung Soo Lim and D-R Sohn and S-G Shin and I-J Jang},
  journal={Clinical pharmacology and therapeutics},
  year={2008},
  volume={83 4},
  pages={595-600}
}
Pharmacokinetic and pharmacodynamic profiles of lorazepam and valproate were analyzed according to uridine 5'-diphosphate-glucuronosyltransferase (UGT)2B7 genotype in 14 healthy subjects with UGT2B15*2/*2 genotype. Systemic clearance of lorazepam (2 mg intravenously) and area under the concentration-time curve (AUC) of valproate (600 mg once daily for 4 days) were analyzed as pharmacokinetic parameters, and area under the effect-time curve (AUEC) of psychomotor coordination tests (Vienna) was… CONTINUE READING

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