olanzapine + fluvoxamine: pharmacokinetic interactions

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Inpharma 1362 - 2 Nov 2002 Olanzapine + fluvoxamine: pharmacokinetic interactions Fluvoxamine increases serum concentrations of olanzapine and clinical response in patients with schizophrenia, report researchers from Germany and Israel. Their study involved 8 patients with chronic schizophrenia who had been receiving olanzapine 10–20 mg/day for 3 months, with no change in olanzapine dosage from 8 weeks before the study to the end of the study. During the study, the patients received additional fluvoxamine 100 mg/day for 8 weeks. By the end of the study, serum concentrations of olanzapine had increased from baseline by a mean of 54.9% (range 12%–112%). Interestingly, serum concentrations of the metabolite N- desmethylolanzapine, which were measured in 5 patients, were constantly increased in 3 and decreased in 2 patients during fluvoxamine administration. Unexpectedly, fluvoxamine concentrations did not reach steady state during the 8 weeks of administration, suggesting that olanzapine may affect the metabolism of fluvoxamine. Of 7 evaluable patients, 5 had a > 20% improvement from baseline in their score on the Schedule for the Assessment of Negative Symptoms. ‘Although the combination was well tolerated and associated with clinical improvement, combined olanzapine and fluvoxamine should be used cautiously and controlled clinically and by therapeutic drug monitoring to avoid olanzapine-induced side effects or intoxication’, comment the researchers. Hiemke C, et al. Fluvoxamine augmentation of olanzapine in chronic schizophrenia: pharmacokinetic interactions and clinical effects. Journal of Clinical Psychopharmacology 22: 502-506, Oct 2002 800920489 1 Inpharma 2 Nov 2002 No. 1362 1173-8324/10/1362-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Page 1: Olanzapine + fluvoxamine: pharmacokinetic interactions

Inpharma 1362 - 2 Nov 2002

Olanzapine + fluvoxamine:pharmacokinetic interactions

Fluvoxamine increases serum concentrations ofolanzapine and clinical response in patients withschizophrenia, report researchers from Germany andIsrael.

Their study involved 8 patients with chronicschizophrenia who had been receiving olanzapine10–20 mg/day for ≥ 3 months, with no change inolanzapine dosage from ≥ 8 weeks before the study tothe end of the study. During the study, the patientsreceived additional fluvoxamine 100 mg/day for 8weeks.

By the end of the study, serum concentrations ofolanzapine had increased from baseline by a mean of54.9% (range 12%–112%). Interestingly, serumconcentrations of the metabolite N-desmethylolanzapine, which were measured in 5patients, were constantly increased in 3 and decreasedin 2 patients during fluvoxamine administration.Unexpectedly, fluvoxamine concentrations did notreach steady state during the 8 weeks of administration,suggesting that olanzapine may affect the metabolism offluvoxamine.

Of 7 evaluable patients, 5 had a > 20% improvementfrom baseline in their score on the Schedule for theAssessment of Negative Symptoms. ‘Although thecombination was well tolerated and associated withclinical improvement, combined olanzapine andfluvoxamine should be used cautiously and controlledclinically and by therapeutic drug monitoring to avoidolanzapine-induced side effects or intoxication’,comment the researchers.Hiemke C, et al. Fluvoxamine augmentation of olanzapine in chronicschizophrenia: pharmacokinetic interactions and clinical effects. Journal of ClinicalPsychopharmacology 22: 502-506, Oct 2002 800920489

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Inpharma 2 Nov 2002 No. 13621173-8324/10/1362-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved