(Bold for FDA approved)
How Dorent works• Reversibly but noncompetitively inhibits centrally active acetylcholinesterase, making more acetylcholine available</br>
• Increased availability of acetylcholine compensates in part for degenerating cholinergic neurons in neocortex that regulate memory</br>
• Does not inhibit butyrylcholinesterase</br>
• May release growth factors or interfere with amyloid deposition
• May take up to 6 weeks before any improvement in baseline memory or behavior is evident
• May take months before any stabilization in degenerative course is evident
Notable Side Effects• Nausea, diarrhea, vomiting, appetite loss, increased gastric acid secretion, weight loss
• Insomnia, dizziness
• Muscle cramps, fatigue, depression, abnormal dreams
• Application-site reactions (transdermal system)
• Nausea, diarrhea, vomiting, appetite loss, increased gastric acid secretion, weight loss
• Insomnia, dizziness
• Muscle cramps, fatigue, depression, abnormal dreams
• Application-site reactions (transdermal system)
Life Threatening Side Effects• Rare seizures
• Rare syncope
• Allergic contact dermatitis (transdermal system)

unusual

unusual
• Wait
• Wait
• Wait
• Take in daytime to reduce insomnia
• Use slower dose titration
• Consider lowering dose, switching to a different agent, or adding an appropriate augmenting agent
• 5–10 mg at night
Dosage Forms• Tablet 5 mg, 10 mg, 23 mg
• Orally disintegrating tablet 5 mg, 10 mg
• Namzaric extended-release (combination memantine/donepezil) 7 mg/10 mg, 14 mg/10 mg, 21 mg/10 mg, 28 mg/10 mg
• Adlarity transdermal system 5 mg, 10 mg
• Drug may lose effectiveness in slowing degenerative course of Alzheimer disease after 6 months
• Can be effective in some patients for several years
• No
Renal Impairment• Few data available but dose adjustment is most likely unnecessary
• For Namzaric, for patients with severe renal impairment, the recommended maintenance dose is 14 mg/10 mg once daily in the evening
Hepatic Impairment• Few data available; may need to lower dose
Cardiac Impairment• Should be used with caution
• Syncopal episodes have been reported with the use of donepezil
Elderly• Some patients may tolerate lower doses better
• Use of cholinesterase inhibitors may be associated with increased rates of syncope, bradycardia, pacemaker insertion, and hip fracture in older adults with dementia
Children and Adolescents• Safety and efficacy have not been established
• Preliminary reports of efficacy as an adjunct in attention deficit hyperactivity disorder (ADHD) (ages 8–17)
Pregnancy• Controlled studies have not been conducted in pregnant women
• Not recommended for use in pregnant women or women of childbearing potential
Breast Feeding• Unknown if donepezil is secreted in human breast milk, but all psychotropics are assumed to be secreted in breast milk
• Recommended either to discontinue drug or formula feed
• Donepezil is not recommended for use in nursing women
Based on data Published online by Cambridge University Press
Compiled by Dr. Jash Ajmera