Medication info
Memantine Tablets 10 mg (Memantine Hydrochloride)

Memantine Tablets 10 mg (Memantine Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Memantine Hydrochloride›10mg
Manufacturer / importer
일동제약(주)
Appearance
White, rectangular film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200500430 · Notified 2005.06.30 · Insurance code 642900500

Summary

Main use
Treatment of moderate to severe Alzheimer's disease
Who takes it
Adults
Adult dose
The maximum daily dose is 20 mg, and it should be increased by 5 mg per week over the first 3 weeks. In the first week (days 1-7): administer 5 mg once daily for 7 days. In the second week (days 8-14): administer 10 mg once daily (5 mg twice a day) for 7 days. In the third week (days 15-21): administer 15 mg once daily (10 mg in the morning and 5 mg in the evening) for 7 days. From the fourth week onward: administer 20 mg once daily (10 mg twice a day).

Ingredients

Manufacturer
일동제약(주)

Efficacy & effects

Treatment of moderate to severe Alzheimer's disease

  • Alzheimer's disease
View approved original text

This medication is used for the treatment of moderate to severe Alzheimer's disease. It helps alleviate the patient's cognitive decline and maintains the ability for daily activities.

How to take

Adult dose

The maximum daily dose is 20 mg, and it should be increased by 5 mg per week over the first 3 weeks. In the first week (days 1-7): administer 5 mg once daily for 7 days. In the second week (days 8-14): administer 10 mg once daily (5 mg twice a day) for 7 days. In the third week (days 15-21): administer 15 mg once daily (10 mg in the morning and 5 mg in the evening) for 7 days. From the fourth week onward: administer 20 mg once daily (10 mg twice a day).

Precautions

This medication should not be used in patients who are allergic to any component of this medication or in patients with severe liver or kidney dysfunction. Care should be taken when using this medication in patients with epilepsy, those who have experienced seizures, or those who are prone to seizures. Additionally, co-administration with NMDA antagonists such as amantadine, ketamine, or dextromethorphan may increase side effects, and should be avoided. Patients with changes in urine acidity (pH) or dietary habits that may increase urine acidity should be monitored carefully. There is insufficient clinical data in patients with myocardial infarction, heart failure, or uncontrolled hypertension, so administration should be cautious. While taking this medication, side effects such as dizziness, headache, constipation, drowsiness, and hypertension may occur. Mental confusion, hallucinations, and psychotic symptoms may also occur rarely, so caution is required. This medication may interact with other substances, so it is important to consult with a doctor or pharmacist if taken alongside antipsychotic medications, muscle relaxants, anticoagulants, etc. Women who are pregnant or may become pregnant should carefully consider the risks and benefits of using this medication, and discontinuation of breastfeeding is recommended while using it. Safety and efficacy in children and adolescents under 18 years of age have not been established. In case of overdose, serious symptoms such as coma, hallucinations, and seizures may occur, so immediate medical attention is necessary. This medication can affect the central nervous system, so care should be taken when driving or operating machinery. Finally, this medication should be kept out of reach of children and should not be transferred to other containers for safety.

Side effects and when to seek care immediately

Serious side effects

  • Seizures
  • heart failure
  • venous thromboembolism
  • shortness of breath
  • headache (including severe headache)
  • hallucinations
  • psychotic reactions
  • confusion
  • gait abnormalities
  • severe dizziness

Mild side effects

  • Dizziness
  • headache
  • constipation
  • drowsiness
  • hypertension
  • confusion
  • hallucinations
  • psychotic reactions
  • balance disorders
  • gait abnormalities
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  • seizures
  • heart failure
  • venous thromboembolism
  • shortness of breath
  • vomiting
  • elevated liver function test results
  • hepatitis
  • fatigue
  • diarrhea
  • agitation
  • aggression
  • delirium
  • unconsciousness

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container that is well-ventilated and kept at room temperature between 1 and 30 degrees Celsius. Storing it this way maintains the drug's effectiveness and prevents degradation.

Appearance and packaging

Appearance

White, rectangular film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.