A case with occurring adverse effects when cross-over titration from fluvoxamine to paroxetine associated with increasing the plasma fluvoxamine level in major depressive disorder

World J Biol Psychiatry. 2009;10(4 Pt 2):620-2. doi: 10.1080/15622970802118349.

Abstract

Selective serotonin reuptake inhibitors (SSRIs) are first line drugs for treating not only depressive disorder but also anxiety disorder. Fluvoxamine, a SSRI, is mainly metabolized by cytochrome P450 (CYP) 2D6 and 1A2. However, paroxetine, an another SSRI is potent inhibitor for CYP 2D6. We report a case with depression whose plasma fluvoxamine level rapidly increased after the addition of paroxetine while switching from fluvoxamine to paroxetine. The case indicates that emerging adverse effects via the pharmacokinetic interaction of these drugs when switching patients from fluvoxamine to paroxetine can occur.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antidepressive Agents, Second-Generation / adverse effects*
  • Antidepressive Agents, Second-Generation / pharmacokinetics*
  • Antidepressive Agents, Second-Generation / therapeutic use
  • Cytochrome P-450 CYP2D6 Inhibitors*
  • Depressive Disorder, Major / blood*
  • Depressive Disorder, Major / drug therapy*
  • Depressive Disorder, Major / psychology
  • Drug Interactions
  • Drug Therapy, Combination
  • Female
  • Fluvoxamine / adverse effects*
  • Fluvoxamine / pharmacokinetics*
  • Fluvoxamine / therapeutic use
  • Humans
  • Paroxetine / adverse effects*
  • Paroxetine / pharmacokinetics*
  • Paroxetine / therapeutic use

Substances

  • Antidepressive Agents, Second-Generation
  • Cytochrome P-450 CYP2D6 Inhibitors
  • Paroxetine
  • Fluvoxamine