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Psychopharmacology Fellow, Department of Pharmacy Practice, College of Pharmacy, University of Florida, Gainesville, FL
Professor and Chair, Department of Pharmacy Practice, School of Pharmacy, South University, Savannah, GA
Reprints: Gary M Levin PharmD BCPP FCCP, School of Pharmacy, South University, 709 Mall Blvd., Savannah, GA 31406-4805, FAX 912/201-8154, E-mail glevin{at}southuniversity.edu
OBJECTIVE: To review the pharmacology, pharmacokinetics, clinical efficacy, and safety profile of aripiprazole for the treatment of schizophrenia.
DATA SOURCES: Information was selected from MEDLINE (1995August 2002). Abstracts, scientific posters, and presentations were also used.
STUDY SELECTION/DATA EXTRACTION: All published information regarding the pharmacokinetic, pharmacodynamic, and clinical characteristics of aripiprazole was considered. Studies providing a comprehensive description of aripiprazole were selected.
DATA SYNTHESIS: Aripiprazole is a dopamine partial agonist and a serotonin-2A antagonist; it is dosed 1030 mg/d, with no initial titration necessary. Short-term clinical trials demonstrated efficacy in acute exacerbations, and long-term studies showed that aripiprazole can maintain remission of schizophrenia. Most adverse events were mild. The incidence of extrapyramidal symptoms was low, with akathisia being the most common.
CONCLUSIONS: Aripiprazole currently demonstrates comparable efficacy and safety for use in schizophrenia.
Key Words: aripiprazole, dopamine-system stabilizer, schizophrenia
Published Online, April 8, 2003. www.theannals.com, DOI 10.1345/aph.1C297
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