Danirinsereup 0.2 mg (Desmopressin Acetate)

Adult dose

Treatment of nocturia associated with nocturnal polyuria (adults only) Administer 0.1mg of 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.

Child dose

Primary nocturnal enuresis (age 5 years and older): Administer 0.2mg of 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.

This medication helps regulate the body's fluid balance, but caution is needed as hyponatremia and water intoxication can occur, especially in elderly patients or those with certain diseases. This medicine should not be used in patients who have had allergic reactions to its ingredients, those with severe heart failure or renal impairment, and patients with certain neurological disorders. Patients with hypertension or cardiovascular diseases, chronic kidney diseases, pregnant women or women who may become pregnant, and children and the elderly should use this medication with extra caution. Water intake should be limited while taking this medication, and it is especially important not to consume a lot of water for a certain period before and after administration. Side effects may include headaches, nausea, skin reactions, and hyponatremia; in severe cases, symptoms such as coma or seizures may occur, so if any unusual symptoms appear, consult a healthcare professional immediately. This medication may interact with other drugs, so if you are currently taking any medication, be sure to inform your doctor or pharmacist. Women who are pregnant or breastfeeding should make a careful decision considering the potential effects on the fetus or newborn, and it is recommended to discontinue breastfeeding while using this medication. In case of overdose, excessive fluid accumulation in the body can worsen hyponatremia, so if symptoms appear, visit a hospital immediately for appropriate treatment.

• coma
• convulsion
• weight gain
• allergic reaction
• hyponatremia
• emotional disorder
• headache
• abdominal pain
• nausea
• allergic skin reaction

This medicine should be stored in a tightly sealed container to avoid exposure to air or moisture. It is important to maintain the storage temperature between 1 and 30 degrees Celsius at room temperature. Proper storage will help maintain the drug's efficacy and safety.

Appearance

White or light yellow granular preparation

Package unit

1 packet (500 mg) x 30 packets/box