Medication info
Desrin Tablet 0.1 mg (Desmopressin Acetate)

Desrin Tablet 0.1 mg (Desmopressin Acetate)

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

MFDS item code 201508213 · Approved 2015.12.11 · Insurance code 652606210

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. Initiation of treatment with this medicine is not recommended in patients aged 65 years or older. In elderly patients who require treatment, closely monitor serum sodium levels and other relevant parameters. (Refer to 5. General Precautions under Precautions for Use.)
Child dose
Primary nocturnal enuresis (5 years and older) Administer 0.2mg desmopressin acetate orally at bedtime. If the effect is insufficient, the dose may be increased up 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
Albogen Korea 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
  • nocturia symptoms
View approved original text

This medication is used to treat primary nocturnal enuresis in patients aged 5 years and older, and nocturia symptoms associated with nocturia in adults.

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. Initiation of treatment with this medicine is not recommended in patients aged 65 years or older. In elderly patients who require treatment, closely monitor serum sodium levels and other relevant parameters. (Refer to 5. General Precautions under Precautions for Use.)

Child dose

Primary nocturnal enuresis (5 years and older) Administer 0.2mg desmopressin acetate orally at bedtime. If the effect is insufficient, the dose may be increased up 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 affects water regulation in the body, so it is important to drink water only when feeling thirsty. Excessive fluid intake can lead to hyponatremia or water intoxication, which in severe cases can cause unconsciousness. This medication should not be used in patients with certain diseases or conditions. For example, patients who are allergic to the components of this medication, those with severely impaired kidney function, heart failure patients, and patients with certain genetic disorders should avoid this medication. Moreover, patients with hypertension, chronic kidney disease, pregnant women, and elderly patients should use this medication with more caution and should have regular blood tests as instructed by their physicians. Side effects from this medication may include headache, nausea, skin allergic reactions, and hyponatremia, and the risk of severe water intoxication leading to unconsciousness or seizures is higher in elderly or certain patients. Fluid intake should be strictly limited during treatment, and it is essential not to drink a lot of water for a certain period before and after administration. Failure to adhere to fluid intake restrictions can lead to dangerous symptoms from excessive water retention in the body. This medication may interact with other medications, so if you are taking other drugs such as antidepressants, diuretics, or steroids, you must inform your doctor or pharmacist. Women who are pregnant or breastfeeding should use this medication with caution, and breastfeeding should be stopped while using this medication. In case of overdose, symptoms like headache, nausea, seizures, and loss of consciousness may appear, so if these symptoms occur, seek medical attention immediately for appropriate treatment. In case of overdose, fluid consumption should be limited, and if necessary, diuretics may be required.

Side effects

  • Coma
  • convulsions
  • weight gain
  • hyponatremia
  • water intoxication
  • allergic reactions
  • emotional disturbance
  • headache
  • abdominal pain
  • nausea
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  • allergic skin reactions
  • dizziness
  • peripheral edema
  • frequent urination
  • dry mouth
  • anaphylaxis
  • malaise
  • vomiting
  • cold sensations
  • loss of consciousness

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

Storage

This medication should be stored in a tightly closed container to prevent air or moisture from entering. It is advisable to store it at room temperature between 1 degree and 30 degrees.

Appearance and packaging

Appearance

White convex 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.

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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.