Vasopressin (20IU)

Clinical Pharmacologist's Monograph

⚠️ Prescription Only: This medicine is Schedule H/H1. Do not self-medicate.

1. Clinical Overview

Vasopressin (20IU) is a synthetic analogue of the endogenous antidiuretic hormone (ADH), arginine vasopressin. It is a potent vasoconstrictor and antidiuretic agent, primarily used in critical care settings in India for the management of vasodilatory shock, gastrointestinal bleeding, and during certain surgical procedures. It acts on V1 receptors in vascular smooth muscle to cause vasoconstriction and on V2 receptors in renal collecting ducts to promote water reabsorption.

OnsetDurationBioavailability
Rapid; within minutes of intravenous administration.Short; approximately 30 to 60 minutes for pressor effects; antidiuretic effect lasts 2-8 hours.Negligible via oral route; 100% via intravenous (IV) route.

2. Mechanism of Action

Vasopressin is an agonist at vasopressin receptors (V1, V2, and V3). Its primary therapeutic effects in critical care are mediated through V1 receptors on vascular smooth muscle, leading to potent vasoconstriction, especially in the splanchnic, cutaneous, and coronary beds. This increases systemic vascular resistance and mean arterial pressure. At higher doses, it also activates V2 receptors in the renal collecting ducts, increasing water permeability via aquaporin-2 channels, leading to antidiuresis.

3. Indications & Uses

  • Vasodilatory shock (e.g., septic shock, post-cardiotomy shock) as an adjunct to catecholamines
  • Control of bleeding from esophageal varices (used with endoscopic therapy)
  • During certain types of cardiac arrest (as per ACLS guidelines, though epinephrine is first-line)

4. Dosage & Administration

Adult Dosage: Vasodilatory Shock: 0.01-0.04 units/minute as continuous IV infusion. Titrate to target MAP. Esophageal Varices: 0.2-0.4 units/minute IV infusion, may be increased to 0.8 units/minute if bleeding continues. Cardiac Arrest: 40 IU as a single IV/IO bolus (replaces first or second dose of epinephrine).

Administration: MUST BE DILUTED before IV administration. For infusion: Dilute 20 IU in 100 mL of Normal Saline or 5% Dextrose to a concentration of 0.2 units/mL. Administer via a central venous catheter preferred to avoid peripheral tissue necrosis. Use an infusion pump. Monitor blood pressure, heart rate, ECG, urine output, and signs of peripheral ischemia continuously.

5. Side Effects

Common side effects may include:

  • Pallor
  • Nausea, abdominal cramps
  • Headache
  • Sweating
  • Tremor
  • Fluid retention, hyponatremia (with prolonged use)

6. Drug Interactions

DrugEffectSeverity
Catecholamines (Noradrenaline, Adrenaline)Additive/synergistic pressor effects; increased risk of severe hypertension and cardiac arrhythmias.Major
Ganglion-blocking agents (e.g., Trimethaphan)Markedly increased pressor sensitivity to vasopressin.Major
Carbamazepine, Chlorpropamide, NSAIDsMay potentiate the antidiuretic (V2) effect, increasing risk of water intoxication and hyponatremia.Moderate
HeparinVasopressin may partially counteract the anticoagulant effect of heparin.Moderate
Lithium, DemeclocyclineAntagonize the antidiuretic effect of vasopressin.Moderate
AlcoholInhibits vasopressin secretion; may reduce antidiuretic effect.Minor

7. Patient Counselling

  • This medication will be administered by healthcare professionals in a hospital.
  • Report immediately any chest pain, shortness of breath, severe headache, or numbness/coldness in limbs.
  • Inform the doctor of all other medications you are taking.

8. Toxicology & Storage

Overdose: Manifestations include hypertension, bradycardia, arrhythmias, myocardial ischemia/infarction, severe peripheral vasoconstriction leading to gangrene, water intoxication (headache, drowsiness, confusion, seizures, coma), hyponatremia, nausea, abdominal cramps, and uterine cramps.

Storage: Store unopened vials at 2°C to 8°C (refrigerate). Do not freeze. Protect from light. After dilution, the solution is chemically stable for up to 24 hours at room temperature. However, it should be used immediately due to microbiological risk. Do not use if solution is discolored or contains particulate matter.