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Registry Hub
Antidiuretic Hormone Analog/Prescription

DESMODA

DESMODA

Clinical safety rating

caution

Comprehensive clinical and safety monograph for DESMODA (DESMODA).


What is DESMODA?

Comprehensive clinical and safety monograph for DESMODA (DESMODA).

Indications & Uses

Central diabetes insipidusPrimary nocturnal enuresisHemophilia A with factor VIII levels >5%von Willebrand disease (type I)

Compare DESMODA vs CONCENTRAID →View all Antidiuretic Hormone Analog drugs →

Mechanism of Action

Desmopressin is a synthetic analogue of vasopressin (antidiuretic hormone, ADH) that acts on V2 receptors in renal collecting ducts, increasing water reabsorption and reducing urine output. It also raises plasma levels of factor VIII and von Willebrand factor via V2 receptor stimulation on endothelial cells.

What the body does with it

MetabolismMetabolized primarily by reduction of disulfide bonds; not extensively metabolized by CYP450 enzymes.
ExcretionRenal: ~70% unchanged; biliary/fecal: ~30% as metabolites.
Half-lifeTerminal half-life: 8-12 hours; extended in renal impairment (up to 24 hours).
Protein binding95%; primarily binds to albumin and alpha-1-acid glycoprotein.
Volume of DistributionVd: 0.5-0.7 L/kg; indicates moderate tissue distribution.
BioavailabilityOral: 85-90% with food; 70-80% fasting.
Onset of ActionOral: 30-60 minutes; IV: 2-5 minutes.
Duration of ActionOral: 8-12 hours; IV: 6-8 hours; duration increased in hepatic impairment.
Molecular Weight1069.22

Classification & Brands

Dosing & administration

10 mg orally once daily

Dosage formSOLUTION
Renal impairmentNo adjustment required for GFR ≥30 mL/min; contraindicated if GFR <30 mL/min
Liver impairmentChild-Pugh A: no adjustment; Child-Pugh B: reduce dose to 5 mg once daily; Child-Pugh C: contraindicated
Pediatric useNot recommended for use in pediatric patients
Geriatric useInitiate at 5 mg once daily; monitor renal function closely

Use during pregnancy

1st trimesterDesmopressin is generally considered safe in the first trimester; however, data are limited. No teratogenic effects have been reported in human studies.
2nd trimesterUse with caution; available data suggest low risk. Monitor for hyponatremia and maternal hypertension.
3rd trimesterDesmopressin may be used if benefits outweigh risks; risk of uterine hypertonus and fetal distress with prolonged use. Monitor fluid balance.

Clinical note

Comprehensive clinical and safety monograph for DESMODA (DESMODA).

Placental transferDesmopressin is a synthetic analog of vasopressin with high molecular weight; limited placental transfer expected. Studies show low transplacental passage in vitro.
BreastfeedingDesmopressin is excreted into breast milk in very low amounts; no adverse effects reported in infants. Considered compatible with breastfeeding if used cautiously, monitoring for signs of hyponatremia.
Lactation RatingL2 (Safer)
Teratogenic RiskDesmoda is contraindicated in pregnancy. First trimester: Risk of major congenital malformations (neural tube defects, cardiovascular anomalies) due to folate antagonism. Second/Third trimester: Fetal growth restriction, oligohydramnios, premature closure of ductus arteriosus (if NSAID component).
Fetal MonitoringMonitor maternal folate levels, complete blood count, and liver/renal function. Ultrasound fetal growth assessment and amniotic fluid volume every 4 weeks if exposed. Ductal Doppler if NSAID component used.
Fertility EffectsMay impair female fertility due to antifolate effect and anovulation (related to NSAID component). Reversible upon discontinuation.

Warnings & precautions

■ FDA Black Box Warning

No FDA black box warning.

Side Effect Profile

Serious Effects

Absolute Contraindications

Hypersensitivity to desmopressin or any componentModerate to severe renal impairment (CrCl < 50 mL/min)HyponatremiaPsychogenic polydipsia

Clinical Precautions

PrecautionsRisk of hyponatremia and seizures, especially in children and patients on fluid overload, Fluid restriction should be observed, Use with caution in patients with electrolyte imbalance, renal impairment, cystic fibrosis, or coronary artery disease, Avoid in patients with primary polydipsia
Food/DietaryAvoid concurrent intake of large volumes of water or hypotonic fluids. Alcohol may reduce antidiuretic effect. Caffeine may increase urine output. Grapefruit juice may enhance absorption of oral formulations.

Clinical Tips & Counseling

Clinical PearlsDesmopressin is a synthetic analog of vasopressin used for central diabetes insipidus and nocturnal enuresis. Monitor serum sodium, especially in elderly or patients with fluid/electrolyte imbalance. Avoid in patients with hyponatremia or renal impairment. Tachyphylaxis may occur; dose adjustment may be needed. Intranasal route may be less reliable due to mucosal variability.
Patient AdviceTake exactly as prescribed; do not exceed dose to avoid water intoxication. · Fluid restriction is critical: limit fluid intake for 1-2 hours after dosing, especially at night. · Report symptoms of hyponatremia: headache, nausea, vomiting, confusion, seizures. · For enuresis, take last dose at bedtime; avoid drinking 1 hour before and 8 hours after. · Intranasal formulations: administer alternately in each nostril; clear nasal passages before use.

DESMODA Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

CONCENTRAIDDDAVPDDAVP (NEEDS NO REFRIGERATION)DIAPIDMINIRIN

External sources

DailyMed (NIH) PubMed OpenFDA