Medication info
Hanin Memantine Od Tablet 10 mg (Memantine Hydrochloride)

Hanin Memantine Od Tablet 10 mg (Memantine Hydrochloride)

Prescription medicationOrally disintegrating Tablet경구
Ingredient · strength
Memantine Hydrochloride›10mg / 1 tablet
Manufacturer / importer
환인제약(주)
Appearance
White round orally disintegrating tablet
Packaging
Domestic - 90 tablets/box [10 tablets/PTP×9], Export - 30 tablets/box [10 tablets/PTP×3]
Approval status
Active

MFDS item code 201706584 · Approved 2017.08.14 · Insurance code 657203190

Summary

Main use
Treatment of moderate to severe Alzheimer's disease
Who takes it
Adults
Adult dose
This medication is taken orally once daily and should be administered at the same time every day. If necessary, it can be taken twice daily. The maximum daily dosage increase is 20mg, and during the first three weeks, it should be increased by 5mg per week. First week (Days 1-7): 5mg once daily for 7 days. Second week (Days 8-14): 10mg once daily for 7 days. Third week (Days 15-21): 15mg once daily for 7 days.

Ingredients

Manufacturer
환인제약(주)

Efficacy & effects

Treatment of moderate to severe Alzheimer's disease

  • Moderate Alzheimer's disease
  • severe Alzheimer's disease
View approved original text

This medication is used for the treatment of moderate to severe Alzheimer's disease. It helps improve memory and cognitive function decline due to brain function impairment, thereby facilitating the patient's daily life. It also helps slow the progression of symptoms and improve the patient's quality of life.

How to take

Adult dose

This medication is taken orally once daily and should be administered at the same time every day. If necessary, it can be taken twice daily. The maximum daily dosage increase is 20mg, and during the first three weeks, it should be increased by 5mg per week. First week (Days 1-7): 5mg once daily for 7 days. Second week (Days 8-14): 10mg once daily for 7 days. Third week (Days 15-21): 15mg once daily for 7 days.

Precautions

This medication contains the artificial sweetener aspartame, which is metabolized in the body, so patients with the genetic disorder phenylketonuria should not take it. Care should be taken not to exceed the maximum daily allowance for aspartame, and it is safe for adults to consume below 2.4 grams per day. Patients who are allergic to any components of this medication or who have severe liver and kidney dysfunction should not take this medication. Patients with epilepsy or those who have experienced seizures should use this medication with caution, and it should be avoided when taken with certain NMDA antagonists due to increased risk of side effects. Patients with changes in urine acidity or uncontrolled cardiac disease and hypertension also need to be cautious. While taking this medication, side effects such as dizziness, headache, constipation, drowsiness, and hypertension may occur, and if symptoms are severe, a doctor should be consulted. There is potential for interaction with other medications, especially when taken with NMDA antagonists, antipsychotic drugs, muscle relaxants, and anticoagulants, so follow the instructions of a professional. Women who are pregnant or might become pregnant should consult a doctor before taking this medication, as it may affect the fetus. Nursing women should consider discontinuing breastfeeding, as this medication may pass into breast milk. Safety and efficacy in children and adolescents under 18 years have not been established, so use should be avoided. In case of overdose, central nervous system and gastrointestinal symptoms may occur, and prompt medical attention should be sought. This medication may affect the patient's reaction times, so caution is required when driving or operating machinery. Finally, store this medication out of reach of children and do not transfer it to another container as this is important for maintaining the quality of the medication.

Side effects and when to seek care immediately

Serious side effects

  • Seizure
  • psychotic reaction
  • hallucination
  • heart failure
  • venous thrombosis/thromboembolism
  • shortness of breath
  • pancreatitis
  • hepatitis

Mild side effects

  • Dizziness
  • headache
  • constipation
  • drowsiness
  • hypertension
  • fungal infection
  • drug hypersensitivity reaction
  • confusion
  • hallucination
  • psychotic reaction
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  • imbalance disorder
  • gait disturbance
  • seizure
  • heart failure
  • venous thrombosis/thromboembolism
  • shortness of breath
  • vomiting
  • pancreatitis
  • elevated liver function test results
  • hepatitis
  • fatigue

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

Storage

This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius. Proper storage ensures the safe retention of the medication's efficacy.

Appearance and packaging

Appearance

White round orally disintegrating tablet

Package unit

Domestic - 90 tablets/box [10 tablets/PTP×9], Export - 30 tablets/box [10 tablets/PTP×3]

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.