Medication info
Neuritane Tablets 0.1mg (Desmopressin Acetate)

Neuritane Tablets 0.1mg (Desmopressin Acetate)

Prescription medicationTabletOral
Ingredient · strength
Desmopressin Acetate›0.1mg / 1 tablet
Manufacturer / importer
Nexpharm Korea Co., Ltd.
Appearance
White oval tablet
Packaging
For domestic use - 30 tablets/bottle
Approval status
Active

MFDS item code 201801175 · Approved 2018.03.15 · Insurance code 662503880

Summary

Main use
Treatment of nocturia associated with nocturnal polyuria in adults and primary nocturnal enuresis in children aged 5 years and older
Who takes it
Adults · Children
Adult dose
Treatment of nocturia associated with nocturnal polyuria (adults only) : Administer 0.1mg desmopressin acetate orally at bedtime. If the effect is insufficient after one week, increase the dose to 0.2mg; if the effect remains insufficient, the dose may be increased at one-week intervals up to 0.4mg. Discontinue treatment if there is no clinical effect within 4 weeks after dose titration. Treatment initiation with this drug is not recommended in patients aged 65 years or older. In elderly patients who require treatment, closely monitor serum sodium levels, etc. (See Precautions for Use, 5. General Precautions.)
Child dose
Primary nocturnal enuresis (age 5 years and older) : Administer 0.2mg desmopressin acetate orally at bedtime. If the effect is insufficient, the dose may be increased to 0.4mg. Whether to continue treatment should be determined after 3 months of treatment, following a treatment-free period of at least 1 week.

Ingredients

Manufacturer
Nexpharm Korea Co., Ltd.

Efficacy & effects

Treatment of nocturia associated with nocturnal polyuria in adults and primary nocturnal enuresis in children aged 5 years and older

  • Primary nocturnal enuresis
  • nocturia
  • symptoms of nocturia
View approved original text

This medication is used to treat the symptoms of primary nocturnal enuresis and nocturia occurring in children aged 5 years and older. It is also helpful in improving symptoms of nocturia occurring in adults. Therefore, it is effectively used for patients suffering from the problem of frequent urination at night.

How to take

Adult dose

Treatment of nocturia associated with nocturnal polyuria (adults only) : Administer 0.1mg desmopressin acetate orally at bedtime. If the effect is insufficient after one week, increase the dose to 0.2mg; if the effect remains insufficient, the dose may be increased at one-week intervals up to 0.4mg. Discontinue treatment if there is no clinical effect within 4 weeks after dose titration. Treatment initiation with this drug is not recommended in patients aged 65 years or older. In elderly patients who require treatment, closely monitor serum sodium levels, etc. (See Precautions for Use, 5. General Precautions.)

Child dose

Primary nocturnal enuresis (age 5 years and older) : Administer 0.2mg desmopressin acetate orally at bedtime. If the effect is insufficient, the dose may be increased to 0.4mg. Whether to continue treatment should be determined after 3 months of treatment, following a treatment-free period of at least 1 week.

Precautions

This medication acts to regulate the amount of water in the body, so it is important to avoid excessive water intake. Particularly, elderly patients or those with certain medical conditions are at risk of falling into a coma due to hyponatremia and water intoxication, so care should be taken to drink only enough water to quench thirst. Patients with allergies to this medication or those with specific heart or kidney diseases, patients on diuretics, and individuals with genetic conditions such as lactose intolerance should not take this medication. Patients with hypertension, atherosclerosis, chronic kidney disease, women of childbearing potential, children, and elderly patients should exercise greater caution when using this medication, especially in cases where there are diseases that can cause fluid and electrolyte imbalances. While taking this medication, side effects such as headaches, nausea, weight gain, and seizures may occur, particularly more frequently in elderly individuals. Fluid intake should be restricted from 1 hour before taking the medication until 8 hours after, and in cases of impaired kidney function, it should be limited to less than 0.5 liters for 12 hours after taking the medication. Additionally, this medication may interact with other drugs, so if other medications are being taken, it is essential to consult a doctor or pharmacist. Pregnant or breastfeeding women should use this medication under medical guidance as it may affect the fetus or newborn. In case of overdose, symptoms such as headaches, nausea, seizures, and loss of consciousness may occur, and immediate medical attention should be sought for proper treatment.

Side effects

  • Hyponatremia
  • fluid overload
  • coma
  • seizures
  • weight gain
  • allergic reactions
  • emotional disturbances
  • headache
  • abdominal pain
  • nausea
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  • allergic skin reactions
  • dizziness
  • peripheral edema
  • frequent urination
  • thirst
  • anaphylaxis

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

Storage

This medication may be sensitive to air or moisture, so it should be stored in a sealed container. It is advisable to maintain the storage temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the efficacy of the medication for a longer period.

Appearance and packaging

Appearance

White oval tablet

Package unit

For domestic use - 30 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.

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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.