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.
Adult dose
Dose adjustments
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).
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Curated clinical cross-links plus same-class fallbacks.
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