Clinical data | |
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Trade names | Aricept, Adlarity, others |
Other names | Donepezil hydrochloride (USAN US) |
AHFS/Drugs.com | Monograph |
MedlinePlus | a697032 |
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Routes of administration | By mouth, transdermal |
Drug class | Acetylcholinesterase inhibitor |
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Pharmacokinetic data | |
Bioavailability | 100%[5][6] |
Protein binding | 96%, albumin (about 75%) and alpha1-acid glycoprotein (21%).[6][5] |
Metabolism | CYP2D6, CYP3A4, and glucuronidation.[5] Four major metabolites, two of which are active.[6][5] |
Onset of action | Peak plasma levels in 3–4 h.[6][5] |
Elimination half-life | 70 hours[7] Around 100 hours in elderly patients.[5] |
Duration of action | With daily dosing, steady-state concentration is reached in 15–21 days.[6][5] |
Excretion | 0.11–0.13 (L/h/kg); excreted mostly by the kidneys. Around 17% is excreted unchanged in the urine. About 15% to 20% is excreted in feces.[5][6] Steady-state clearance is similar at all ages.[5] |
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ECHA InfoCard | 100.125.198 |
Chemical and physical data | |
Formula | C24H29NO3 |
Molar mass | 379.500 g·mol−1 |
3D model (JSmol) | |
Chirality | Racemic mixture |
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Donepezil, sold under the brand name Aricept among others, is a medication used to treat dementia of the Alzheimer's type.[3][4][8] It appears to result in a small benefit in mental function and ability to function.[9] Use, however, has not been shown to change the progression of the disease.[10] Treatment should be stopped if no benefit is seen.[11] It is taken by mouth or via a transdermal patch.[3][4][8]
Common side effects include nausea, trouble sleeping, aggression, diarrhea, feeling tired, and muscle cramps.[8][11] Serious side effects may include abnormal heart rhythms, urinary incontinence, and seizures.[8] Donepezil is a centrally acting reversible acetylcholinesterase inhibitor and structurally unrelated to other anticholinesterase agents.[8][5]
Donepezil was approved for medical use in the United States in 1996.[8] It is available as a generic medication.[11] In 2022, it was the 146th most commonly prescribed medication in the United States, with more than 3 million prescriptions.[12][13]
Kum2020
was invoked but never defined (see the help page).there is a linear relationship between dose and pharmacodynamic effects, measured as red blood cell acetylcholinesterase inhibition and clinical efficacy. Despite being 96% bound to plasma proteins, it has few interactions with other drugs, and the 5-mg dose can be given safely to patients with mild-to-moderate hepatic and renal-disease.
Plasma donepezil concentrations decline with a half-life of approximately 70 h. Sex, race, and smoking history have no clinically significant influence on plasma concentrations of donepezil [46–51].