Is intravenous (IV) desmopressin available?

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Last updated: December 30, 2025View editorial policy

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IV Desmopressin Availability

Yes, intravenous (IV) desmopressin is available and FDA-approved for clinical use. The FDA-approved formulation is desmopressin acetate injection 4 mcg/mL, which can be administered intravenously, subcutaneously, or by direct IV injection depending on the indication 1.

FDA-Approved Formulations and Routes

IV desmopressin has been available since 1981 and is indicated for multiple clinical conditions 1, 2:

  • Hemophilia A and von Willebrand Disease (Type I): Administered as IV infusion at 0.3 mcg/kg diluted in sterile saline over 15-30 minutes 1
  • Diabetes Insipidus: Can be given by direct IV injection or subcutaneously at 0.5-1 mL (2-4 mcg) daily in divided doses 1
  • Bleeding disorders: The standard hemostatic dose is 0.3 mcg/kg IV infused over 15-30 minutes 1

Clinical Applications in Critical Care

Multiple clinical guidelines recommend IV desmopressin for specific hemostatic indications 3:

  • Antiplatelet reversal: The Neurocritical Care Society recommends desmopressin 0.4 mcg/kg IV × 1 for patients with intracranial hemorrhage on antiplatelet agents, with platelet transfusion added if neurosurgical intervention is required 3
  • Uremic platelet dysfunction: The American Society of Nephrology recommends 0.3 mcg/kg IV as first-line treatment, with hemostatic effects beginning within 1 hour and lasting 6-8 hours 4
  • Von Willebrand disease: For bleeding patients with types 1 and 2A, desmopressin is recommended first-line before specific VWF/FVIII concentrates 3

Administration Guidelines

For hemostatic purposes, the standard protocol is 1:

  • Dose: 0.3 mcg/kg body weight
  • Dilution: In 50 mL sterile saline for adults and children >10 kg; 10 mL for children ≤10 kg
  • Infusion time: 15-30 minutes
  • Timing: Administer 30 minutes before scheduled procedures
  • Monitoring: Blood pressure and pulse during infusion

Important Safety Considerations

Fluid restriction is mandatory to prevent water intoxication and hyponatremia 5, 1:

  • Limit evening fluid intake to ≤200 mL (6 ounces) 5
  • Monitor serum sodium levels, particularly with repeated dosing 4
  • The risk of hyponatremia is substantial, with rates of 146 per 1,000 person-years reported in population studies 6

Tachyphylaxis occurs after 3-5 doses due to depletion of endothelial VWF stores, limiting repeated administration to intervals >48 hours 3, 7, 1.

Common Pitfalls

  • Thromboembolic risk: Desmopressin can cause thromboembolic events in at-risk patients and should be used with caution in elderly populations 3, 5
  • Renal impairment: Avoid in severe renal impairment (CrCl <30 mL/min) as desmopressin is substantially excreted by the kidney 5, 1
  • Limited efficacy in specific conditions: Does not effectively reverse ticagrelor or prasugrel, and may be ineffective in COVID-19 patients on ECMO due to depleted endothelial stores 5
  • Vasodilator effects: Can cause arterial hypotension, reactive tachycardia, and facial flushing 5

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment of Uremic Platelet Dysfunction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Desmopressin Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Mechanism of Action and Clinical Effects of Desmopressin

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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