Medication info
Dyturin Tablets 0.1 mg (Desmopressin Acetate)

Dyturin Tablets 0.1 mg (Desmopressin Acetate)

Prescription medicationTabletOral
Ingredient · strength
Desmopressin Acetate›0.1mg / 1 tablet
Manufacturer / importer
Jongkundang Co., Ltd.
Appearance
White, convex, oval tablets
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 201400932 · Approved 2014.02.28 · Insurance code 643306730

Summary

Main use
Treatment of primary nocturnal enuresis (age 5 years and older) and nocturia associated with nocturnal polyuria (adults)
Who takes it
Adults · Children
Adult dose
Treatment of nocturia associated with nocturnal polyuria (adults only) : Administer desmopressin acetate 0.1mg 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. Initiating treatment with this medicine is not recommended in patients aged 65 years and older. In elderly patients who require treatment, monitor serum sodium levels closely. (See section 5, General Precautions, under Precautions for Use.)
Child dose
Primary nocturnal enuresis (5 years and older) : Administer desmopressin acetate 0.2mg 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 administration, following a treatment-free period of at least 1 week.

Ingredients

Manufacturer
Jongkundang Co., Ltd.

Efficacy & effects

Treatment of primary nocturnal enuresis (age 5 years and older) and nocturia associated with nocturnal polyuria (adults)

  • Primary nocturnal enuresis
  • nocturia symptoms
View approved original text

This medication is used to treat primary nocturnal enuresis in patients aged 5 years and older, as well as nocturia symptoms associated with nocturia in adults. It helps alleviate the symptoms of frequent urination at night and aids in sound sleep. It is effective in improving the patient's symptoms and enhancing their quality of life.

How to take

Adult dose

Treatment of nocturia associated with nocturnal polyuria (adults only) : Administer desmopressin acetate 0.1mg 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. Initiating treatment with this medicine is not recommended in patients aged 65 years and older. In elderly patients who require treatment, monitor serum sodium levels closely. (See section 5, General Precautions, under Precautions for Use.)

Child dose

Primary nocturnal enuresis (5 years and older) : Administer desmopressin acetate 0.2mg 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 administration, following a treatment-free period of at least 1 week.

Precautions

This medication acts to regulate the balance of body fluids; therefore, care should be taken to avoid excessive fluid intake, especially in the elderly or patients with certain disorders. It should not be used in patients who are allergic to this medication or have certain heart or kidney diseases. Additionally, patients with genetic issues such as lactose intolerance should not take this medication. Caution is advised when administering this drug to patients with hypertension, cardiovascular diseases, chronic kidney diseases, pregnant women, children, and elderly patients. Fluid intake should be restricted while taking this medication, as excessive fluid intake can be harmful. The medication may cause side effects such as hyponatremia, coma due to excessive fluid, seizures, and weight gain; if symptoms appear, consult a doctor immediately. This medication may interact with other drugs, so it's essential to inform healthcare providers of any other medications being taken. Pregnant or breastfeeding women must be cautious when using this medication, and breastfeeding should be discontinued if necessary. In cases of overdose, serious symptoms such as headache, nausea, seizures, and loss of consciousness may occur; hence, dosage should be adjusted according to symptoms, and medical treatment should be sought if necessary.

Side effects

  • coma
  • seizures
  • weight gain
  • severe water intoxication
  • hyponatremia
  • allergic reactions
  • emotional disturbances
  • headache
  • abdominal pain
  • nausea
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  • allergic skin reactions
  • dizziness
  • peripheral edema
  • frequency of urination
  • thirst
  • anaphylaxis
  • malaise
  • vomiting
  • weight increase
  • cold sensation
  • loss of consciousness

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

Storage

Store this medication in a tightly sealed container to prevent exposure to air or moisture. It is recommended to maintain the storage temperature between 1 and 30 degrees Celsius at room temperature, as this will help preserve the efficacy of the drug.

Appearance and packaging

Appearance

White, convex, oval tablets

Package unit

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.