Viewing nowAricept Tablets 23 mg (Donepezil Hydrochloride)
Donepezil Hydrochloride 23mg
Tablet · Prescription medication
Handok Co., Ltd.

MFDS item code 201307375 · Approved 2013.05.16 · Insurance code 652105800
Treatment of moderate to severe Alzheimer's type dementia symptoms
This medication is used to treat moderate to severe Alzheimer's type dementia symptoms. It helps improve memory decline and cognitive function deterioration caused by dementia, aiding the patient's daily living abilities. It also has the effect of slowing the progression of symptoms by facilitating signal transmission between nerve cells. It contributes to improving overall cognitive function and enhancing the quality of life for both patients and families. This drug has been proven safe and effective and is widely used in clinical settings. Therefore, it is effectively used for the treatment of moderate to severe Alzheimer's type dementia symptoms.
This medication is taken once daily just before bedtime, and can be administered regardless of food intake. The initial recommended dose of Donepezil Hydrochloride is 5 mg once daily. The drug reaches a steady state after 15 days of administration, so it is recommended to start with 5 mg for 4–6 weeks. After evaluating clinical responses, the dose may be increased to 10 mg, with caution regarding gastrointestinal adverse effects when increasing to 10 mg daily. Patients should take 10 mg daily for at least 3 months before considering further dosage adjustments.
This medication should not be used by women who are allergic to certain ingredients, pregnant, or nursing. Patients with genetically related lactose disorders should also not take this medication. Patients with heart disease or certain cardiac conduction disorders should use this medication cautiously as it may slow heart rate or cause arrhythmias. Patients with a history of peptic ulcers or those taking non-steroidal anti-inflammatory drugs should be cautious as gastrointestinal bleeding or ulcer exacerbation may occur. Patients with asthma or obstructive pulmonary disease should be careful as symptoms may worsen due to bronchoconstriction or increased mucus secretion. Patients with extrapyramidal disorders such as Parkinson's disease should be cautious as symptoms may worsen. This medication may cause various adverse reactions, including heart problems, gastrointestinal bleeding, liver dysfunction, cerebrovascular disorders, motor function disorders, serious muscle issues, and respiratory distress. Additionally, dizziness, drowsiness, insomnia, hallucinations, anxiety, and depression have been reported as central nervous system symptoms. During treatment, weight loss, decreased appetite, nausea, vomiting, and diarrhea may commonly occur, but these symptoms are usually temporary. This medication is approved only for the treatment of Alzheimer's type dementia and should not be used for other types of dementia or memory disorders. Treatment should be conducted under the diagnosis and supervision of an experienced physician, and discontinuation should be considered in the absence of treatment effects. Patients with heart disease should periodically check their heart condition through electrocardiograms, and patients with gastrointestinal disorders should observe for worsening gastrointestinal symptoms. This medication may affect driving or machinery operation abilities, so caution is required. Women who are pregnant or nursing should not use this medication without consulting a professional if absolutely necessary. Safety in children has not been established, so this drug should not be used in pediatric patients. This medication may interact with other drugs, so it is essential to consult a doctor or pharmacist if taking certain antibiotics, antidepressants, antiarrhythmics, cardiac medications, or anticholinergic drugs. In case of overdose, severe nausea, vomiting, sweating, decreased heart rate, respiratory distress, and seizures may occur, requiring immediate medical attention. This medication should be stored out of reach of children and should not be transferred to other containers.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, cough with accompanying fever, yellowing of skin or eyes (jaundice), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urinary retention
Not everyone experiences these, and they can vary from person to person.
Store this medication in a tightly sealed container to prevent air ingress, and keep it at room temperature between 1 to 30 degrees Celsius. This storage can help maintain the effectiveness of the drug.
Red, biconvex round film-coated tablet
30 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Tablet · Prescription medication
Handok Co., Ltd.

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Tablet · Prescription medication
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.