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Desmopressin

DDAVP

What it isVasopressin V2-receptor agonist; diabetes insipidus, nocturnal enuresis, and bleeding in von Willebrand disease.

Why this oneV2 selectivity produces antidiuresis without vasoconstriction and releases stored von Willebrand factor.

What limits it⚑ Hyponatremia can be severe or fatal—restrict fluid and monitor sodium in higher-risk patients.

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Central diabetes insipidusAdults & children0.05 mg BID0.1-0.8 mg/day divided (range 0.1-1.2 mg/day divided BID-TID)1.2 mg/day
Primary nocturnal enuresis>=6 yr0.2 mg QHStitrate to 0.6 mg QHS0.6 mg QHS

Renal Contraindicated if CrCl <50 mL/min (moderate-to-severe renal impairment)

Hepatic Undefined

Instructions

Contraindications

Cautions

Adverse reactions

Pregnancy Category B; no fetal harm in animal studies; use only if clearly needed

Lactation Undefined

NO BOXED WARNINGS

Principal riskSevere hyponatremia unless fluid is restricted

Cost, est. cash$20–$1,500/month

Generic entry1997

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

Mechanism of action: Desmopressin ballicule

Desmopressin ballicule: receptor binding, kinetics and half-life diagram

Open Desmopressin in the interactive console ↗

Memory aids: mascots and interaction avatars

Desmopressin DDAVP mascot mnemonic cartoon
“Desert Preston a.k.a. Dee Dee the Aviator”
Filled with water → causes hyponatremia
Lowers serum sodium
Desmopressin no kinetic interactions avatar
no kinetic interactions

Open Desmopressin in the interactive console ↗