Donepezil dosing strategies: pharmacokinetic considerations.

TitleDonepezil dosing strategies: pharmacokinetic considerations.
Publication TypeJournal Article
Year of Publication2011
AuthorsGomolin IH, Smith C, Jeitner TM
JournalJ Am Med Dir Assoc
Volume12
Issue8
Pagination606-608
Date Published2011 Oct
ISSN1538-9375
KeywordsCholinesterase Inhibitors, Cost-Benefit Analysis, Donepezil, Dose-Response Relationship, Drug, Humans, Indans, Models, Theoretical, Piperidines, United States, United States Food and Drug Administration
Abstract

Donepezil (Aricept) is a cholinesterase inhibitor approved for the treatment of Alzheimer's disease. Immediate release formulations of 5- and 10-mg tablets were approved by the Food and Drug Administration in the United States in 1996. In July 2010, the Food and Drug Administration approved a 23-mg sustained release (SR) formulation. The SR formulation may provide additional benefit to patients receiving 10 mg daily but the incidence of adverse reactions is increased. We derived plasma concentration profiles for higher dose immediate-release formulations (15 mg once daily, 10 mg twice daily, and 20 mg once daily) and for the profile anticipated to result from the 23-mg SR formulation. Our model predicts similar steady-state concentration profiles for 10 mg twice daily, 20 mg once daily, and 23 mg SR once daily. This provides the theoretical basis for incremental immediate release dose escalation to minimize the emergence of adverse reactions and the potential to offer a cost-effective alternative to the SR formulation with currently approved generic immediate release formulations.

DOI10.1016/j.jamda.2011.02.004
Alternate JournalJ Am Med Dir Assoc
PubMed ID21943887
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