What is the recommended dose of vasopressin (antidiuretic hormone)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Recommended Vasopressin Dosing

For septic shock, vasopressin should be administered at an initial dose of 0.01 units/minute and titrated up by 0.005 units/minute every 10-15 minutes to a maximum of 0.07 units/minute, while for post-cardiotomy shock, start at 0.03 units/minute with a maximum of 0.1 units/minute. 1

Indications and Dosing Guidelines

Vasopressin is primarily used as an adjunctive vasopressor in shock states, particularly when patients are refractory to catecholamines. The FDA-approved dosing varies by indication:

Septic Shock

  • Initial dose: 0.01 units/minute
  • Titration: Increase by 0.005 units/minute every 10-15 minutes until target blood pressure is reached
  • Maximum dose: 0.07 units/minute 1

Post-Cardiotomy Shock

  • Initial dose: 0.03 units/minute
  • Titration: Increase by 0.005 units/minute every 10-15 minutes until target blood pressure is reached
  • Maximum dose: 0.1 units/minute 1

Administration Considerations

  • Vasopressin should be diluted in normal saline (0.9% sodium chloride) or 5% dextrose in water (D5W) prior to intravenous administration 1
  • Discard unused diluted solution after 18 hours at room temperature or 24 hours under refrigeration 1
  • Vasopressin is not recommended as a first-line agent but rather as an adjunct to norepinephrine 2
  • After target blood pressure has been maintained for 8 hours without catecholamines, taper vasopressin by 0.005 units/minute every hour as tolerated 1

Safety Considerations and Monitoring

  • Doses higher than 0.04 units/minute have not been associated with increased effectiveness and may be associated with higher adverse effects 3
  • Cardiac arrests have been reported at doses of 0.05 units/minute or higher 3
  • Vasopressin is not recommended for cardiogenic shock without ScvO2/CO monitoring 4
  • Monitor for adverse effects including:
    • Cardiac and peripheral ischemia
    • Arrhythmias
    • Hypertension
    • Bowel ischemia 4

Timing of Vasopressin Addition

Recent evidence suggests earlier addition of vasopressin (within 3 hours of starting norepinephrine) may be beneficial:

  • Associated with faster time to shock resolution (37.6 hours vs 60.7 hours) 5
  • May decrease ICU length of stay 5
  • A 2025 reinforcement learning study suggests more frequent and earlier use of vasopressin than current practice patterns, associated with reduced mortality 6

Special Populations

Pediatric Patients

  • Low-dose arginine vasopressin (≤0.04 units/kg/min) has short-term hemodynamic benefits in children with vasodilatory shock 4
  • Monitor renal function closely as pediatric patients may experience increased urea and creatinine levels and decreased urine output with longer duration or higher cumulative doses 7
  • Platelet counts may be significantly lower during infusion 7

Important Caveats

  • Always establish arterial line monitoring when using vasopressors 2
  • Monitor parameters including blood pressure, heart rate, urine output, skin perfusion, mental status, lactate clearance, and renal and liver function tests 2
  • Target mean arterial pressure (MAP) ≥65 mmHg 2
  • Titrate to the lowest dose compatible with a clinically acceptable response 1

By following these evidence-based dosing guidelines and monitoring parameters, vasopressin can be safely and effectively used as an adjunctive vasopressor in appropriate shock states.

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.