Medication info
Unirin Tablets 0.1 mg (Desmopressin Acetate)

Unirin Tablets 0.1 mg (Desmopressin Acetate)

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

MFDS item code 202003564 · Approved 2020.05.15 · Insurance code 648604080

Summary

Main use
Treatment of primary nocturnal enuresis (age 5 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 1 week, increase the dose to 0.2mg; if the effect remains insufficient, the dose may be increased at 1-week intervals up to 0.4mg. If there is no clinical effect within 4 weeks after dose determination, discontinue treatment. Initiation of treatment with this medicine is not recommended in patients aged 65 years or older. If treatment is necessary in an older patient, closely monitor serum sodium levels, etc. (Refer to 5. General Precautions under Precautions for Use)
Child dose
Primary nocturnal enuresis (5 years of age 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
CMG Pharmaceuticals Co., Ltd.

Efficacy & effects

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

  • Primary nocturnal enuresis
  • nighttime urinary symptoms
View approved original text

This medication is used for the treatment of primary nocturnal enuresis in children aged 5 and older and nighttime urinary symptoms related to nocturia in adults. In other words, it helps improve symptoms primarily for those who frequently urinate at night or have difficulty controlling urination. This medication contributes to reducing discomfort caused by enuresis and enhances 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 1 week, increase the dose to 0.2mg; if the effect remains insufficient, the dose may be increased at 1-week intervals up to 0.4mg. If there is no clinical effect within 4 weeks after dose determination, discontinue treatment. Initiation of treatment with this medicine is not recommended in patients aged 65 years or older. If treatment is necessary in an older patient, closely monitor serum sodium levels, etc. (Refer to 5. General Precautions under Precautions for Use)

Child dose

Primary nocturnal enuresis (5 years of age 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 by regulating the body’s fluid balance and may cause side effects such as hyponatremia or water intoxication; therefore, it is especially important for the elderly or patients with certain diseases to limit fluid intake. This medication should not be administered to patients with hypersensitivity, severely impaired cardiac function, those taking diuretics, patients with renal failure, or those with specific diseases. Pregnant women or those who may become pregnant, patients with hypertension or chronic kidney disease, as well as children and elderly patients should exercise increased caution when using this medication, and it should be administered under the physician's discretion if necessary. During the course of treatment with this medication, strict limitations on fluid intake should be maintained; excessive fluid intake can lead to symptoms such as headaches, nausea, weight gain, and in severe cases, seizures. Side effects may include hyponatremia, headaches, dizziness, and allergic reactions, and there is a higher risk of serious symptoms such as coma or seizures in the elderly. This medication may interact with other drugs, so caution is needed when taken with tricyclic antidepressants, diuretics, corticosteroids, and non-steroidal anti-inflammatory drugs. Pregnant women should use this medication only when absolutely necessary as it may cause uterine contractions, and breastfeeding women are advised to discontinue breastfeeding while using this medication. In cases of overdose, symptoms such as fluid retention and hyponatremia, leading to headaches, nausea, seizures, and loss of consciousness may occur, necessitating immediate medical attention, and treatment such as diuretic administration or fluid restriction may be required.

Side effects

  • coma
  • convulsions
  • weight gain
  • severe water intoxication
  • hyponatremia
  • allergic reaction
  • emotional disturbance
  • headache
  • abdominal pain
  • nausea
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  • allergic skin reaction
  • dizziness
  • peripheral edema
  • increased urination
  • thirst
  • anaphylaxis
  • malaise
  • vomiting
  • weight weight gain
  • cold sensation
  • loss of consciousness

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

Storage

This medication should be stored in a sealed container to protect it from air and moisture. A suitable storage temperature is room temperature between 1°C and 30°C. This will help maintain the medication’s effectiveness for a longer duration.

Appearance and packaging

Appearance

White oval tablet

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.

Questions about this medicine

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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.