Bleeding Complications in a Patient After the Unexpected Interaction between Valproic Acid and Phenprocoumon

Curr Drug Saf. 2024;19(1):142-144. doi: 10.2174/1574886318666230310104322.

Abstract

Background: Phenprocoumon is a vitamin K antagonist that is widely prescribed in Europe and Latin America for the prophylaxis and treatment of thromboembolic events.

Case presentation: A 90-year-old female was admitted to our hospital with tonic-clonic seizures, possibly due to dementia syndrome. Valproic acid (VPA) was prescribed for the treatment of seizures. VPA is an inhibitor of cytochrome P450 (CYP) 2C9 enzymes. A pharmacokinetic interaction with phenprocoumon occurred, which is a substrate for CYP2C9 enzymes. The interaction resulted in a strong INR increase and subsequent clinically relevant bleeding in our patient. Valproic acid is not specifically mentioned in the phenprocoumon drug label as a CYP2C9 inhibitor, and in the Dutch medication surveillance database, no medication alert is shown when prescribing this combination, and no interaction with phenprocoumon has been reported so far.

Conclusion: When prescribing this combination, the prescriber should be warned and advised to intensify INR monitoring if the combination is to be continued.

Keywords: CYP inhibitor; CYP2C9; INR; coumarin; drug-drug interaction; phenprocoumon.; valproic acid; vitamin K antagonist.

Publication types

  • Case Reports

MeSH terms

  • Acenocoumarol / pharmacokinetics
  • Aged, 80 and over
  • Anticoagulants / adverse effects
  • Aryl Hydrocarbon Hydroxylases*
  • Cytochrome P-450 CYP2C9
  • Female
  • Humans
  • Phenprocoumon* / adverse effects
  • Phenprocoumon* / pharmacokinetics
  • Valproic Acid / adverse effects

Substances

  • Phenprocoumon
  • Valproic Acid
  • Acenocoumarol
  • Cytochrome P-450 CYP2C9
  • Aryl Hydrocarbon Hydroxylases
  • Anticoagulants