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Drug-drug interaction and initial dosage optimization of aripiprazole in patients with schizophrenia based on population pharmacokinetics. | LitMetric

AI Article Synopsis

  • The study examined how fluoxetine affects the clearance and dosage of aripiprazole in patients with schizophrenia using population pharmacokinetics.
  • It involved 119 patients, revealing that weight and fluoxetine use significantly impact aripiprazole dosage requirements.
  • Recommendations for effective initial dosages of aripiprazole were provided based on patient weight, considering the presence or absence of fluoxetine in their treatment regimen.

Article Abstract

Background: The present study aimed to investigate the drug-drug interaction and initial dosage optimization of aripiprazole in patients with schizophrenia based on population pharmacokinetics.

Research Design And Methods: A total of 119 patients with schizophrenia treated with aripiprazole were included to build an aripiprazole population pharmacokinetic model using nonlinear mixed effects.

Results: The weight and concomitant medication of fluoxetine influenced aripiprazole clearance. Under the same weight, the aripiprazole clearance rates were 0.714:1 in patients with or without fluoxetine, respectively. In addition, without fluoxetine, for the once-daily aripiprazole regimen, dosages of 0.3 and 0.2 mg kg day were recommended for patients with schizophrenia weighing 40-95 and 95-120 kg, respectively, while for the twice-daily aripiprazole regimen, 0.3 mg kg day was recommended for those weighing 40-120 kg. With fluoxetine, for the once-daily aripiprazole regimen, a dosage of 0.2 mg kg day was recommended for patients with schizophrenia weighing 40-120 kg, while for the twice-daily aripiprazole regimen, 0.3 and 0.2 mg kg day were recommended for those weighing 40-60 and 60-120 kg, respectively.

Conclusion: This is the first investigation of the effects of fluoxetine on aripiprazole via drug-drug interaction. The optimal aripiprazole initial dosage is recommended in patients with schizophrenia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11217561PMC
http://dx.doi.org/10.3389/fpsyt.2024.1377268DOI Listing

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