[A current problem for regulators. Clopidogrel and pharmacokinetics]

Pharm Unserer Zeit. 2009;38(4):360-7. doi: 10.1002/pauz.200900326.
[Article in German]
No abstract available

Publication types

  • Review

MeSH terms

  • Aryl Hydrocarbon Hydroxylases / antagonists & inhibitors
  • Aryl Hydrocarbon Hydroxylases / biosynthesis
  • Aryl Hydrocarbon Hydroxylases / genetics
  • Aryl Hydrocarbon Hydroxylases / metabolism
  • Clopidogrel
  • Cytochrome P-450 CYP2C19
  • Drug Industry
  • Drug Interactions
  • Drug Therapy, Combination
  • Enzyme Induction / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Platelet Aggregation Inhibitors / adverse effects
  • Platelet Aggregation Inhibitors / pharmacokinetics*
  • Platelet Aggregation Inhibitors / therapeutic use
  • Polymorphism, Genetic
  • Thrombosis / genetics
  • Thrombosis / prevention & control
  • Ticlopidine / adverse effects
  • Ticlopidine / analogs & derivatives*
  • Ticlopidine / pharmacokinetics
  • Ticlopidine / therapeutic use
  • United States
  • United States Food and Drug Administration

Substances

  • Enzyme Inhibitors
  • Platelet Aggregation Inhibitors
  • Clopidogrel
  • Aryl Hydrocarbon Hydroxylases
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19
  • Ticlopidine