Dosage/Direction for Use
Oral Cranial diabetes insipidus Adult: Initially, 100 mcg tid, adjust according to response. Maintenance: 100-200 mcg tid up to 100-1,200 mcg daily. Child: Same as adult dose. Oral Primary nocturnal enuresis Adult: Initially, 200 mcg at bedtime, may titrate up to 600 mcg to achieve desired response. Child: ≥6 yr Initially, 200 mcg at bedtime, may titrate up to 600 mcg to achieve desired response. Sublingual Cranial diabetes insipidus Adult: Initially, 60 mcg tid. Maintenance: 60-120 mcg tid up to 720 mcg daily. Child: Same as adult dose. Nasal Cranial diabetes insipidus Adult: 10-20 mcg once daily or bid. Child: 5-20 mcg daily. Infants may require lower dose. Nasal Diagnosis of diabetes insipidus Adult: 20 mcg as a single dose. Child: Same as adult dose. Nasal Renal function testing Adult: 40 mcg as a single dose. Child: ≤1 yr 10 mcg; >1-15 yr 20 mcg. Both given as a single dose. Nasal Nocturia associated with multiple sclerosis Adult: 10-20 mcg at bedtime. Nasal Type I Von Willebrand's disease Adult: 300 mcg; <50 kg: 150 mcg. Should be given 0.5-2 hr before surgery. Parenteral Cranial diabetes insipidus Adult: 1-4 mcg once daily via IV, IM or SC inj. Child: 0.4 mcg daily via IV, IM, SC inj. Parenteral Diagnosis of diabetes insipidus Adult: 2 mcg via IM or SC inj. Child: Same as adult dose. Parenteral Renal function testing Adult: 2 mcg via IM or SC inj. Child: Same as adult dose. Intravenous Type I Von Willebrand's disease Adult: 0.4 mcg/kg by slow infusion over 15-30 min before surgery. Further dose may be given at 12-hr interval. Child: Same as adult dose. Reconstitution: IV infusion: Dilute in 10 mL or 50 mL of NaCl 0.9% inj. Intravenous Testing of fibrinolytic response Adult: 0.4 mcg/kg infusion over 20 min. Child: Same as adult dose. Reconstitution: IV infusion: Dilute in 10 mL or 50 mL of NaCl 0.9% inj. Parenteral Headache following lumbar puncture Adult: 4 mcg via IM or SC inj, may be repeated after 24 hr if needed. May also be given as prophylaxis. |
Administration
May be taken with or without food.
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Contraindications
Cardiac insufficiency w/ ongoing diuretic treatment. Patient w/ habitual and psychogenic polydipsia, hyponatraemia or history of hyponatraemia. Moderate to severe renal impairment (CrCl <50 mL/min).
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Special Precautions
Patient w/ CV disease or cystic fibrosis, coronary artery insufficiency, at risk for increased intracranial pressure, predisposed to thrombus formation. Elderly and childn. Pregnancy and lactation. Monitoring Parameters Monitor BP and pulse during IV infusion.
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Adverse Reactions
Headache, nausea, stomach pain, allergic skin reaction and more severe general allergic reactions, cerebral or coronary thrombosis. Local irritation, congestion and epistaxis. Pain and swelling at the inj site.
Potentially Fatal: Anaphylaxis. |
Overdosage
Symptoms: Prolonged duration of action w/ an increased risk of water retention and/or hyponatraemia. Management: Symptomatic treatment. Fluid restriction.
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Drug Interactions
May enhance antidiuretic effect w/ NSAIDs (e.g. ibuprofen), indometacin, TCAs, chlorpromazine, carbamazepine, SSRIs, opiates, lamotrigine. May reduce antidiuretic effect w/ lithium, epinephrine (large dose), heparin, demeclocycline.
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Food Interaction
May reduce antidiuretic effect w/ alcohol.
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Action
Desmopressin increases cyclic adenosine monophosphate (cAMP) in renal tubular cells which increases water permeability resulting in reduced urine volume and enhanced urine osmolality. It also stimulates factor VII and plasminogen activator activity in the blood, but w/ minimal pressor activity.
Onset: Antidiuretic: Approx 60 min (oral); 15-30 min (intranasal). Duration: Approx 6-14 hr. Absorption: Absorbed minimally from the GI tract; absorbed from the nasal mucosa. Bioavailability: 0.08-0.16% (oral); 10-20% (intranasal). Time to peak plasma concentration: 0.9 hr (oral); 1.5 hr (intranasal). Excretion: Mainly via urine. Elimination half-life: 2-4 hr. |
Storage
Intravenous: Soln for inj: Store between 2-8°C. Protect from light. Nasal: Store between 20-25°C. Protect from light. Oral: Store between 20-25°C. Protect from light. Parenteral: Soln for inj: Store between 2-8°C. Protect from light. Sublingual: Store between 20-25°C. Protect from light.
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CIMS Class
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ATC Classification
H01BA02 - desmopressin ; Belongs to the class of vasopressin and analogues. Used in posterior pituitary lobe hormone preparations.
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