Aricept is a prescription medicine used to manage symptoms of Alzheimer’s disease. As an acetylcholinesterase inhibitor, it helps increase the availability of acetylcholine in the brain, supporting memory, attention, and day-to-day functioning in many people with mild, moderate, or severe Alzheimer’s. It does not cure dementia, but it can meaningfully ease symptoms for some patients and caregivers. Aricept comes as standard tablets and orally disintegrating tablets and is typically taken once daily. Because it affects heart rate, sleep, and the digestive system, it should be started and adjusted by a clinician who can monitor safety and effectiveness over time.
Aricept is the brand name for donepezil, an acetylcholinesterase inhibitor approved to treat the symptoms of Alzheimer’s disease across mild, moderate, and severe stages. By reducing the breakdown of acetylcholine, a key neurotransmitter for learning and memory, Aricept may improve or stabilize cognition, attention, and activities of daily living for some patients. While responses vary, many caregivers notice subtle improvements in organization, conversational ability, or daily engagement after the medication is titrated to a therapeutic dose.
It’s important to understand what Aricept does and does not do. It does not cure dementia or halt the underlying disease process; rather, it provides symptomatic benefit that can help maintain function and quality of life. Benefits may be modest and may take weeks to become apparent. Some clinicians also consider Aricept in certain mixed dementias or dementia with Lewy bodies, but these uses are off-label and should be weighed carefully, especially given potential sensitivity to cholinergic effects in some conditions.
Aricept is typically started at 5 mg once daily, often taken in the evening to reduce daytime nausea. After 4 to 6 weeks, many patients are increased to 10 mg once daily if the initial dose is well tolerated and there’s a clinical rationale to do so. For moderate to severe Alzheimer’s disease, a 23 mg extended-release strength exists; this dose is considered only after a patient has tolerated 10 mg daily for at least three months. Decisions to escalate should always be individualized by the prescribing clinician based on benefits, tolerability, comorbidities, and caregiver input.
Aricept may be taken with or without food. Standard tablets should be swallowed whole with water. The orally disintegrating tablet (ODT) is placed on the tongue to dissolve, then swallowed; no water is required. The 23 mg extended-release tablet should not be crushed, chewed, or split. If insomnia or vivid dreams occur with nighttime dosing, some clinicians switch to morning administration; this adjustment should be discussed with the prescriber to ensure safety and adherence.
No routine dose adjustment is usually required for mild to moderate kidney impairment. In hepatic impairment or frail older adults, a slower titration and closer monitoring are prudent. Because Alzheimer’s presentations and caregiver support vary widely, a personalized dosing and follow-up plan is essential to optimize benefits and minimize side effects.
Aricept increases cholinergic activity, which can lower heart rate and affect conduction in the heart. Use caution in patients with bradycardia, sick sinus syndrome, atrioventricular block, or those on other rate-slowing drugs (such as certain beta-blockers). Monitor for dizziness, syncope, or falls, particularly during initiation and dose changes. An electrocardiogram may be considered in patients with a cardiac history or overlapping risk factors.
The medication can increase gastric acid secretion and may heighten the risk of gastrointestinal bleeding, especially when combined with NSAIDs (such as ibuprofen, naproxen) or in those with a history of peptic ulcer disease. Report black or tarry stools, vomiting blood, or new abdominal pain promptly. Nausea, vomiting, diarrhea, and decreased appetite are common early in therapy and often improve with time or dose adjustments.
Other cholinergic effects warrant caution in asthma or COPD (potential bronchoconstriction), urinary outflow obstruction (worsening frequency/urgency), and seizure disorders (lowered threshold). Weight loss can occur and should be monitored, especially in underweight or frail individuals. Sleep disturbances, including insomnia and vivid dreams, may emerge; adjusting dose timing can help. During surgery or anesthesia, Aricept can interact with neuromuscular blockers—always inform the surgical team about current therapy.
Pregnancy and breastfeeding data for donepezil are limited. If exposure occurs or therapy is being considered, risks and benefits should be reviewed with a clinician. As with all dementia treatments, shared decision-making that includes the patient whenever possible and the caregiver is central to safe, compassionate care.
Aricept is contraindicated in individuals with known hypersensitivity to donepezil or to piperidine derivatives. Past serious allergic reactions, including rash, hives, angioedema, or anaphylaxis, preclude further use. If any signs of serious skin reactions (such as widespread rash, blistering, or mucosal involvement) occur, stop the medication and seek urgent medical evaluation.
Common side effects include nausea, vomiting, diarrhea, decreased appetite, weight loss, dizziness, fatigue, muscle cramps, headache, insomnia, and vivid dreams. These are most frequent during the first weeks of therapy or after a dose increase, and many diminish with continued use or by adjusting administration time. Taking with a small snack may ease gastrointestinal symptoms.
Less common but more serious effects can include bradycardia, syncope, atrioventricular block, gastrointestinal bleeding or ulceration, urinary incontinence, seizures, and rare skin reactions (including Stevens-Johnson syndrome). Rhabdomyolysis and neuroleptic malignant syndrome–like reactions have been reported rarely. Seek medical attention if experiencing fainting spells, chest pain, severe abdominal pain, black stools, coughing or vomiting blood, new confusion or agitation beyond baseline, or severe muscle pain and dark urine.
Caregivers play a key role in observing changes. Keeping a simple log of sleep quality, appetite, bowel habits, alertness, mood, and daily function during the first two months can help clinicians judge benefit versus side effects and tailor the plan accordingly.
Aricept’s effects can be influenced by other medicines. Anticholinergic drugs (such as diphenhydramine, certain bladder antispasmodics like oxybutynin or tolterodine, and some tricyclic antidepressants) may counteract donepezil’s benefits by blocking acetylcholine. Conversely, other cholinergic agents can increase side effects. Caution is warranted with neuromuscular blockers (particularly succinylcholine) used during anesthesia due to prolonged neuromuscular blockade.
Additive bradycardia may occur with beta-blockers (e.g., metoprolol), some calcium channel blockers (e.g., verapamil, diltiazem), digoxin, or amiodarone. Monitor heart rate and symptoms like dizziness or near-syncope when these combinations are unavoidable. Nonsteroidal anti-inflammatory drugs can raise the risk of gastrointestinal bleeding; gastroprotection may be considered for at-risk patients.
Donepezil is metabolized mainly by CYP2D6 and CYP3A4. Potent inhibitors (such as ketoconazole, clarithromycin, fluoxetine, paroxetine, or quinidine) may increase donepezil levels and side effects; dose adjustments or closer monitoring may be needed. Inducers (such as carbamazepine, phenytoin, rifampin, or St. John’s wort) may reduce effectiveness. Because polypharmacy is common in older adults, always provide a complete, up-to-date medication list—including over-the-counter drugs and supplements—at each visit.
If a dose of Aricept is missed, take it as soon as remembered the same day. If it is nearly time for the next dose, skip the missed dose and resume the regular schedule. Do not double up to make up for a missed dose. If several days of doses are missed—particularly more than seven days—consult the prescriber before restarting. Re-titration from a lower dose may be recommended to reduce side effects when resuming therapy.
Overdose can lead to a cholinergic crisis, with symptoms such as severe nausea, vomiting, drooling, sweating, slow heart rate, low blood pressure, collapse, difficulty breathing, muscle weakness, and seizures. This is a medical emergency. In the United States, call Poison Control at 1-800-222-1222 or seek emergency care immediately. Treatment is supportive; atropine may be used by medical professionals as an antidote. Keep Aricept out of reach of children and individuals who might accidentally ingest extra doses.
Store Aricept at room temperature, ideally between 68°F and 77°F (20°C to 25°C), in a dry place away from excess heat and moisture. Keep tablets in their original container with the lid tightly closed, and avoid bathroom storage where humidity fluctuates. The orally disintegrating tablets should remain in the blister until use to protect from moisture. Dispose of expired or unused medication through a community take-back program or according to pharmacist guidance; do not flush unless specifically instructed.
In the United States, Aricept is a prescription-only medication. Federal and state laws require a valid prescription from a licensed clinician based on an appropriate medical evaluation and ongoing monitoring. Attempts to buy Aricept without prescription are unsafe and may be illegal. Proper diagnosis, assessment of risks and benefits, and a plan for follow-up are essential for safe use, particularly in older adults with multiple medical conditions or medications.
HealthSouth Rehabilitation Hospital of Tallahassee supports patients and caregivers by providing structured, lawful pathways to dementia care. While it does not dispense Aricept without a prescription, its care teams can coordinate comprehensive evaluation, memory and functional assessments, medication management, and referrals to licensed prescribers and pharmacies. Through this integrated approach, patients can access Aricept when appropriate, receive counseling on side effects and interactions, and benefit from ongoing monitoring that maximizes safety and therapeutic value.
If you or a loved one is exploring treatment with Aricept, schedule a professional evaluation rather than seeking the medication directly. A clinician can confirm the diagnosis, rule out reversible causes of cognitive change, discuss realistic goals, and tailor dosing and follow-up to the individual’s needs. This medically supervised route is the safest, most effective way to start and maintain therapy with Aricept.
1 Aricept (donepezil) is a cholinesterase inhibitor prescribed to treat mild, moderate, and severe Alzheimer’s disease. It helps improve or maintain memory, thinking, and daily functioning for a time, but it does not cure dementia.
2 Donepezil blocks the enzyme acetylcholinesterase, which breaks down acetylcholine, a key neurotransmitter for memory and cognition. By increasing acetylcholine levels, it can modestly improve communication between brain cells.
3 Aricept does not cure Alzheimer’s or stop the disease. It can slow symptom decline and provide modest improvements or stability in cognitive and functional measures for months to years in some patients.
4 Adults with a clinical diagnosis of Alzheimer’s disease across mild to severe stages may be candidates. Clinicians weigh potential benefits against risks in people with bradycardia, significant cardiac conduction problems, active peptic ulcer disease, severe weight loss, or severe liver disease.
5 The usual starting dose is 5 mg once daily. After 4–6 weeks, many patients increase to 10 mg once daily; those with moderate to severe disease may move to 23 mg once daily after at least 3 months on 10 mg. It can be taken in the morning or evening, ideally at the same time each day.
6 Some people notice changes within a few weeks, but full assessment typically requires 6–12 weeks at a therapeutic dose. Benefits may include better attention, memory, communication, or daily function, often reported by caregivers.
7 Nausea, diarrhea, loss of appetite, weight loss, muscle cramps, fatigue, dizziness, and insomnia or vivid dreams are common and often lessen after dose adjustments or time. Taking the dose in the morning or with a small snack can help with sleep or stomach issues.
8 Seek medical attention for fainting, very slow heartbeat, severe vomiting, black stools, blood in vomit, severe abdominal pain, seizures, or new or worsening breathing problems. Call a clinician promptly for significant weight loss or dehydration.
9 Yes. Donepezil can cause insomnia and intense dreams, especially when taken at night. Switching to a morning dose often reduces these effects.
10 It can be taken with or without food. If nausea occurs, taking it with a light meal or snack may help.
11 Strong CYP3A4 or CYP2D6 inhibitors (for example, ketoconazole, erythromycin, paroxetine) can raise donepezil levels; inducers (for example, carbamazepine, phenytoin, rifampin, St. John’s wort) can lower them. Combining with anticholinergic drugs (for example, diphenhydramine, oxybutynin) may reduce benefit, while beta-blockers or other drugs that slow the heart can heighten bradycardia risk. NSAIDs can increase the risk of stomach bleeding.
12 Aricept is FDA-approved for Alzheimer’s disease. Evidence suggests benefit in dementia with Lewy bodies and Parkinson’s disease dementia, but rivastigmine has the specific approval for Parkinson’s disease dementia. Use in vascular dementia is off-label and individualized.
13 Donepezil is available as standard tablets and orally disintegrating tablets (ODT) that melt on the tongue without water. This can help patients with dysphagia.
14 Treatment is continued as long as there is perceived cognitive, behavioral, or functional benefit without intolerable side effects. It may be stopped if there is progressive decline with no clear benefit, severe adverse effects, or based on patient and caregiver goals.
15 Yes. FDA-approved generics must demonstrate bioequivalence to brand Aricept. Most patients experience the same clinical effectiveness and safety at lower cost.
16 Head-to-head studies show broadly similar modest benefits for cognition and daily function in Alzheimer’s disease. Individual response varies; some patients do better on one agent than another.
17 The rivastigmine transdermal patch often causes less nausea and vomiting than oral cholinesterase inhibitors, including Aricept. Skin irritation at the patch site can occur and should be rotated and monitored.
18 Overall effectiveness is comparable. Galantamine also modulates nicotinic receptors, while donepezil selectively inhibits acetylcholinesterase; in practice, choice depends on tolerability, dosing preferences, comorbidities, and prior response.
19 Aricept is once daily at all doses. Rivastigmine is twice daily orally or once daily via patch. Galantamine is twice daily immediate-release or once daily extended-release. Many find Aricept or the rivastigmine patch simplest.
20 All can cause gastrointestinal upset, weight loss, dizziness, and bradycardia. Rivastigmine tends to have more GI effects orally but fewer with the patch; donepezil can cause vivid dreams; galantamine may be slightly more activating in some patients.
21 Rivastigmine has FDA approval for Parkinson’s disease dementia and is often favored there. Donepezil and galantamine show benefit in Lewy body disorders and are used off-label when appropriate.
22 The rivastigmine transdermal patch typically has the lowest rate of nausea and vomiting. If tablets are preferred, starting low and going slow with Aricept or galantamine may still be successful.
23 All agents can lower appetite and weight, but rivastigmine (especially oral) may carry a slightly higher risk of weight loss due to GI effects. Monitoring weight regularly is recommended regardless of choice.
24 Yes. Clinicians often stop one and start another at its starting dose the next day, then retitrate. Switching is considered for intolerance, lack of benefit, or practical issues like swallowing or adherence.
25 All three have generics in most regions, which lowers cost. Donepezil is widely available and often among the least expensive, but prices vary by pharmacy, dose, and insurance.
26 Donepezil and galantamine are metabolized by CYP enzymes (3A4 and 2D6), so inhibitors and inducers can alter levels. Rivastigmine has minimal CYP metabolism, so it has fewer pharmacokinetic interactions but shares class effects like bradycardia with beta-blockers and increased GI bleeding risk with NSAIDs.
27 Tacrine, an older cholinesterase inhibitor, is rarely used due to significant liver toxicity and frequent monitoring needs. Donepezil offers similar or better efficacy with a much safer profile and has largely replaced tacrine in practice.