Switching from intravenous to oral tacrolimus and voriconazole leads to a more pronounced drug-drug interaction

Eur J Clin Pharmacol. 2013 Mar;69(3):737-8. doi: 10.1007/s00228-012-1365-8. Epub 2012 Aug 10.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / antagonists & inhibitors
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Antifungal Agents / administration & dosage*
  • Antifungal Agents / adverse effects*
  • Antifungal Agents / blood
  • Antifungal Agents / pharmacokinetics
  • Biological Availability
  • Cytochrome P-450 CYP3A / metabolism
  • Cytochrome P-450 CYP3A Inhibitors
  • Drug Interactions
  • Drug Monitoring
  • Humans
  • Immunosuppressive Agents / administration & dosage*
  • Immunosuppressive Agents / adverse effects*
  • Immunosuppressive Agents / blood
  • Immunosuppressive Agents / pharmacokinetics
  • Liver Transplantation / immunology
  • Male
  • Middle Aged
  • Pulmonary Aspergillosis / drug therapy
  • Pulmonary Aspergillosis / microbiology
  • Pyrimidines / administration & dosage*
  • Pyrimidines / adverse effects*
  • Pyrimidines / blood
  • Pyrimidines / pharmacokinetics
  • Tacrolimus / administration & dosage*
  • Tacrolimus / adverse effects*
  • Tacrolimus / blood
  • Tacrolimus / pharmacokinetics
  • Triazoles / administration & dosage*
  • Triazoles / adverse effects*
  • Triazoles / blood
  • Triazoles / pharmacokinetics
  • Voriconazole

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antifungal Agents
  • Cytochrome P-450 CYP3A Inhibitors
  • Immunosuppressive Agents
  • Pyrimidines
  • Triazoles
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human
  • Voriconazole
  • Tacrolimus