Viewing nowPMS Memantine Tablet 5mg (Memantine Hydrochloride)
Memantine Hydrochloride 5mg
Tablet · Prescription medication
Genupharm Co., Ltd.

MFDS item code 202500256 · Approved 2025.02.07 · Insurance code 698004750
Treatment for moderate to severe Alzheimer's disease
This medication is used to improve memory decline and cognitive impairment in patients with moderate to severe Alzheimer's disease. It helps stabilize the patient's condition and enhance the quality of daily life.
This medication is administered orally once a day and should be taken at the same time every day. If necessary, it may be taken twice a day. 1. Adults Dose increment: The maximum daily dose is 20mg, and it is increased by 5mg per week for the first 3 weeks. - First week (Days 1-7): 5mg once daily - Second week (Days 8-14): 10mg once daily - Third week (Days 15-21): 15mg once daily
This drug should not be used in patients with known allergies to its components or in those with severe liver or kidney disorders. Caution should be exercised in patients with epilepsy, a history of seizures, or a high risk of seizures. Concurrent use with other drugs that have similar effects may increase central nervous system side effects, so co-administration should be avoided. Patients in situations where urine acidity (pH) may change should be monitored closely as the drug's efficacy may be affected. For patients with uncontrolled heart disease or hypertension, the safety has not been adequately validated; therefore, caution should be used. This medication contains specific dyes, and patients with allergies to these components should be careful. Potential side effects include dizziness, headache, constipation, drowsiness, hypertension, and others. Consult a doctor if symptoms are severe. There may be interactions with other medications, so patients taking antipsychotics, muscle relaxants, anticoagulants, etc., should inform their doctor. Women who are pregnant or may become pregnant must consult a doctor before taking this medication. It is advisable to discontinue breastfeeding while on this drug. The safety and efficacy of this medication have not been established in children or adolescents under 18 years of age. In cases of overdose, serious symptoms such as confusion, drowsiness, dizziness, hallucinations, and seizures may occur; thus, adherence to dosage is crucial, and immediate hospital visit is required in case of overdose. This medicine can affect the central nervous system, so caution is necessary when driving or operating machinery. Keep out of reach of children and avoid transferring to other containers.
Seizures, severe allergic reactions (drug hypersensitivity), hypertension, thrombosis, respiratory distress, liver abnormalities (elevated liver function tests, hepatitis), severe edema (heart failure), serious neurological symptoms (seizures, confusion, hallucinations, psychotic reactions), severe skin adverse reactions (not previously reported), reduced urine output (not previously reported)
Not everyone experiences these, and they can vary from person to person.
Store this medication in a tightly sealed container to prevent air or moisture from entering. It is also advisable to keep it at room temperature between 1 to 30 degrees Celsius, avoiding extreme heat or cold.
Yellow oblong film-coated tablet
100 tablets/bottle, 30 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.