Medication info
Montesem Tablet (Domperidone Maleate)

Montesem Tablet (Domperidone Maleate)

Prescription medicationTabletOral
Ingredient · strength
Domperidone Maleate›12.72mg
Manufacturer / importer
Medica Korea Co., Ltd.
Appearance
White round tablet
Packaging
Domestic - 300 tablets/bottle, Export - 100 tablets/box [10 tablets/PTP×10]
Approval status
Active

MFDS item code 199701401 · Notified 1997.08.11 · Insurance code 646001090

Summary

Main use
Relief of nausea and vomiting
Who takes it
Adults · Children
Adult dose
In general, do not use for more than 1 week.
Child dose
Adolescents (12 years and older, weighing 35 kg or more): Administer domperidone 10 mg (5 mg when levodopa is administered) orally per dose 3 times daily before meals. The maximum daily dose is 30 mg.

Ingredients

Manufacturer
Medica Korea Co., Ltd.

Efficacy & effects

Relief of nausea and vomiting

  • Symptoms of nausea and vomiting
View approved original text

This medication is used to relieve symptoms of nausea and vomiting.

How to take

Adult dose

In general, do not use for more than 1 week.

Child dose

Adolescents (12 years and older, weighing 35 kg or more): Administer domperidone 10 mg (5 mg when levodopa is administered) orally per dose 3 times daily before meals. The maximum daily dose is 30 mg.

Precautions

This medication should not be used in certain patients. For example, it can be dangerous to administer this medication to patients who have allergies to it or have bleeding, obstruction, or perforation in the stomach. Additionally, it should not be used in patients with prolactin-secreting tumors, certain heart diseases, severely impaired liver function, or women who are pregnant or may become pregnant. This medication contains lactose and is not suitable for patients with genetic problems such as lactose intolerance or galactose intolerance. Caution should be exercised when administering this medication to children, especially those weighing less than 35 kg, as well as to patients with impaired kidney or liver function, elderly patients, and patients with a history of heart disease. Drowsiness or dizziness may occur during treatment with this medication, so caution should be taken when driving or operating machinery. Additionally, because this medication is metabolized in the liver, dose adjustments may be necessary for patients with liver damage, and the number of doses and dosages should be reduced for patients with kidney failure. There is a risk of cardiac-related side effects, so patients with arrhythmias or electrolyte imbalances should not use this medication, and immediate consultation with a physician is necessary if cardiac symptoms appear. There are many drug interactions, so caution is needed when administering with certain antibiotics, antifungals, antiarrhythmics, antipsychotics, etc., and some medications are contraindicated for concurrent use. It is advisable not to take this medication during pregnancy or breastfeeding, and if breastfeeding, consultation with a physician is required as side effects may occur in the infant. In case of overdose, neurological symptoms or cardiac problems may arise, necessitating immediate visit to a medical institution for appropriate treatment. This medication should be stored out of reach of children and kept in its original container, ensuring it is not mixed with other medications.

Side effects

  • dyspepsia
  • gastroesophageal reflux disease
  • irritable bowel syndrome
  • nausea
  • vomiting
  • dry mouth
  • loss of libido
  • anxiety
  • drowsiness
  • headache
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  • diarrhea
  • rash
  • itching
  • hyperprolactinemia
  • breast pain
  • breast tenderness
  • asthenia
  • restlessness
  • breast discharge
  • gynecomastia
  • breast swelling
  • depressive disorder
  • hypersensitivity
  • lactation disorder
  • irregular menstruation
  • anaphylactic reaction
  • agitation
  • irritability
  • dizziness
  • extrapyramidal disorder
  • convulsions
  • ocular myoclonus
  • ventricular arrhythmia
  • acute cardiac death
  • Torsades de Pointes
  • QTc prolongation
  • vascular edema
  • urticaria
  • urinary retention
  • gynecomastia
  • amenorrhea
  • abnormal liver function tests
  • increased serum prolactin
  • edema
  • confusion
  • altered consciousness
  • spatial disorientation
  • Parkinson's syndrome

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

Storage

This medication may be sensitive to air and moisture, so it must be stored in a tightly sealed container. It is recommended to maintain a storage temperature between 1°C and 30°C. Proper storage will help preserve the effectiveness of the medication for a longer period.

Appearance and packaging

Appearance

White round tablet

Package unit

Domestic - 300 tablets/bottle, Export - 100 tablets/box [10 tablets/PTP×10]

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

No questions yet.

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.