Pharmacokinetic parameters of bromperidol in Korean subjects

Hum Psychopharmacol. 2006 Aug;21(6):409-12. doi: 10.1002/hup.776.

Abstract

We have presented pharmacokinetic parameters of bromperidol (BP) in 14 healthy Korean subjects. Additionally, we have investigated the effects of dose and genetic polymorphisms on BP metabolism and on extrapyramidal symptoms (EPS). The T(max) (3.9 +/- 0.9 h), clearance (1.37 +/- 0.52 ml/h/kg), and t(1/2) (20.4 +/- 3.7 h) obtained in our study are comparable to those in previous Caucasian studies, although pharmacokinetic profiles were affected by the BP dose. We could not prove any significant correlations between BP metabolism or adverse effects and genetic factors because the number of subjects was small. Further studies with a larger population are needed to determine the influence of genetic factors on BP therapy.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antipsychotic Agents / administration & dosage
  • Antipsychotic Agents / adverse effects
  • Antipsychotic Agents / blood
  • Antipsychotic Agents / pharmacokinetics*
  • Basal Ganglia Diseases / chemically induced
  • Cytochrome P-450 CYP2D6 / genetics
  • Cytochrome P-450 CYP2D6 / metabolism
  • Cytochrome P-450 CYP3A
  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / metabolism
  • Dose-Response Relationship, Drug
  • Dystonia / chemically induced
  • Female
  • Genotype
  • Haloperidol / administration & dosage
  • Haloperidol / adverse effects
  • Haloperidol / analogs & derivatives*
  • Haloperidol / blood
  • Haloperidol / pharmacokinetics
  • Humans
  • Korea
  • Male
  • Reference Values

Substances

  • Antipsychotic Agents
  • Cytochrome P-450 Enzyme System
  • CYP3A protein, human
  • Cytochrome P-450 CYP2D6
  • Cytochrome P-450 CYP3A
  • Haloperidol
  • bromperidol