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ADH Analogue Pregnancy: Caution should be exercised when prescribing to pregnant women; blood pressure monitoring is recommended because of the increased risk of pre-eclampsia. Data on a limited number (n=53) of exposed pregnancies in women with diabetes insipidus indicate rare cases of malformations; animal studies do not indicate direct or indirect harmful effects. Lactation: the amounts transferred to the child after high-dose desmopressin are considerably less than those required to influence diuresis, so it is not considered necessary to stop breastfeeding.

Desmopressin (Paediatric)

Brand names: DesmoMelt, DDAVP, Desmospray

Desmopressin is a synthetic vasopressin analogue used in children for primary nocturnal enuresis, cranial diabetes insipidus and certain bleeding disorders such as mild haemophilia A and von Willebrand disease.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Primary nocturnal enuresis — children from 5 years of age and adults up to 65 years of age with normal urine concentrating ability: 120 micrograms at bedtime. If this dose is not sufficiently effective, the dose may be increased up to 240 micrograms
Route: Sublingual — place the tablet under the tongue, where it dissolves without the need for water
Frequency: Once daily, at bedtime
Max: Nocturnal enuresis: up to 240 micrograms sublingually at bedtime. Diabetes insipidus: the total daily sublingual dose normally lies in the range 120 micrograms to 720 micrograms
PAEDIATRIC POPULATION: the SPC states desmopressin is indicated for treatment in this population and that 'Dose recommendations are the same as in adults' — the dose is a fixed sublingual dose, not a per-kg dose, which is why paedDose is null; the regimen above applies to children from 5 years of age. Paediatric dosing should also be verified against a children's formulary. FLUID RESTRICTION IS MANDATORY in enuresis: fluid intake must be limited to a minimum from 1 hour before administration until the next morning (at least 8 hours after). Treatment without concomitant reduction of fluid intake may lead to water retention and/or hyponatraemia, with or without warning signs (headache, nausea/vomiting, weight gain and, in severe cases, convulsions). If such signs occur, interrupt treatment until the patient has fully recovered, and enforce strict fluid restriction when restarting. DURATION: sublingual tablets are intended for treatment periods of up to 3 months; reassess the need for continued treatment by means of a period of at least 1 week without the medicine. If adequate clinical effect is not achieved within 4 weeks following appropriate dose titration, discontinue. DIABETES INSIPIDUS: dosage is individual; a suitable starting dose in adults AND children is 60 micrograms three times daily sublingually, adjusted according to response; for the majority of patients the maintenance dose is 60 micrograms to 120 micrograms sublingually three times daily. POST-HYPOPHYSECTOMY POLYURIA/POLYDIPSIA: the dose should be controlled by measurement of urine osmolality. ELDERLY: initiation of treatment in patients over 65 years of age is not recommended. HEPATIC IMPAIRMENT: no dose adjustment needed. Food intake may reduce the intensity and duration of the antidiuretic effect at low doses. Interrupt treatment during acute intercurrent illnesses characterised by fluid and/or electrolyte imbalance (systemic infections, fever, gastroenteritis). Consider severe bladder dysfunction and outlet obstruction before starting treatment for enuresis. NOTE: the US label in the same bundle (desmopressin acetate TABLETS, American Health Packaging) is a different formulation with different figures (central diabetes insipidus: start 0.05 mg twice daily, usual range 0.1 mg to 0.8 mg daily in divided doses, total daily range 0.1 mg to 1.2 mg; primary nocturnal enuresis from age 6 years: 0.2 mg at bedtime, titrated up to 0.6 mg) — these are oral-tablet US figures and have NOT been used for the dose above.

Dose adjustments

Renal

Contraindicated in moderate and severe renal insufficiency (creatinine clearance below 50 ml/min). Care should be taken with patients who have reduced renal function; in chronic renal disease the antidiuretic effect of desmopressin would be less than normal. No numerical dose adjustment is given.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to desmopressin or to any of the excipients
  • Known or suspected cardiac insufficiency and other conditions requiring treatment with diuretic agents
  • Moderate and severe renal insufficiency (creatinine clearance below 50 ml/min)
  • Known hyponatraemia, or syndrome of inappropriate ADH secretion (SIADH)
  • Habitual or psychogenic polydipsia (urine production exceeding 40 ml/kg/24 hours) and alcohol abuse
  • For primary nocturnal enuresis: should only be used in patients with normal blood pressure, and should not be prescribed to patients over the age of 65

Side effects

  • Hyponatraemia — the most serious adverse reaction; associated with headache, nausea, vomiting, decreased serum sodium, weight increase, malaise, abdominal pain, muscle cramps, dizziness, confusion, decreased consciousness and, in severe cases, convulsions and coma
  • Headache (common); somnolence (uncommon)
  • Abdominal pain, nausea, vomiting and diarrhoea (common)
  • Affect lability and aggression (common); anxiety symptoms, nightmares and mood swings (uncommon) — in children these psychiatric effects are generally reversed on treatment discontinuation
  • Peripheral oedema and fatigue (common); irritability (rare)
  • Hypertension (uncommon); bladder and urethral symptoms (uncommon)

Interactions

  • Substances known to induce SIADH — tricyclic antidepressants, selective serotonin reuptake inhibitors, chlorpromazine and carbamazepine — may cause an additive antidiuretic effect, increasing the risk of water retention and/or hyponatraemia
  • Sulfonylurea antidiabetics, particularly chlorpropamide — additive antidiuretic effect
  • NSAIDs — may induce water retention and/or hyponatraemia
  • Loperamide — concomitant treatment may result in a 3-fold increase in desmopressin plasma concentrations, increasing the risk of water retention and/or hyponatraemia
  • When any of these are co-prescribed, take precautions to avoid hyponatraemia including careful attention to fluid restriction and more frequent monitoring of serum sodium

Clinical monograph

How it works

It acts on renal V2 receptors to increase water reabsorption in the collecting ducts, concentrating urine, and additionally raises plasma factor VIII and von Willebrand factor.

Prescribing in practice

  • The key paediatric hazard is hyponatraemic water intoxication and seizures, so fluid intake must be restricted around dosing and the drug withheld during vomiting, diarrhoea or other fluid balance disturbance.
  • Avoid in children with habitual or psychogenic polydipsia and use cautiously in those with conditions predisposing to fluid or electrolyte imbalance.
  • For nocturnal enuresis avoid fluids from shortly before until the morning after a dose and use a children's formulary for route and frequency.

Monitoring

Monitor for signs of fluid overload and hyponatraemia, with periodic review of weight and serum sodium especially when treatment is prolonged or during intercurrent illness.

Counselling the patient

  • Limit drinks in the evening and stop the medicine if the child is unwell with vomiting or diarrhoea.
  • Seek help urgently for headache, nausea, drowsiness or fits, which may indicate low sodium.
  • Take the dose at the time advised, typically before bedtime for bedwetting.

Evidence & guidelines

NICE guidance supports desmopressin as a first-line option for managing nocturnal enuresis in children, with hyponatraemia recognised as the principal safety concern.

Reference: NICE Enuresis in Children CG111; ICCS Enuresis Guidelines 2020; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.