BOXED WARNING Serious or fatal respiratory failure; risk increased with volume overload or ACLF Grade 3 — assess SpO2 before start, do not initiate if hypoxic, monitor continuous pulse oximetry and discontinue if SpO2 <90%.
FDA dosing
Population
Start
Target
Max
Hepatorenal syndrome with rapid reduction in kidney function
Adults
0.85 mg (1 vial) IV q6h (Days 1–3)
0.85 mg q6h; may increase to 1.7 mg (2 vials) q6h on Day 4 if SCr decreased <30% from baseline
1.7 mg (2 vials) IV q6h
Renal Undefined
Hepatic No adjustment needed
Day 4: adjust dose by change in SCr from baseline; discontinue if SCr at/above baseline; continue until 24h after two consecutive SCr ≤1.5 mg/dL, max 14 days
Instructions
Reconstitute each vial with 5 mL 0.9% Sodium Chloride (0.85 mg/5 mL)
Give by slow IV bolus over 2 minutes via peripheral or central line; flush line after
Obtain baseline SpO2 and assess ACLF grade/volume status before first dose; monitor continuous pulse oximetry
Do not initiate in hypoxic patients (e.g., SpO2 <90%) until oxygenation improves; avoid in ACLF Grade 3
Contraindications
Hypoxia or worsening respiratory symptoms
Ongoing coronary, peripheral, or mesenteric ischemia
Cautions
Serious or fatal respiratory failure — manage volume overload
Adverse reactions may make patient ineligible for liver transplant (esp. MELD ≥35)
Vasoconstrictor — cardiac, cerebrovascular, peripheral, or mesenteric ischemia
Embryo-fetal toxicity — induces uterine contractions and endometrial ischemia
Adverse reactions
Abdominal pain
Nausea
Respiratory failure
Diarrhea
Dyspnea
Fluid overload
Pregnancy May cause fetal harm; induces uterine contractions and endometrial ischemia
Lactation No data on presence in milk; weigh clinical need against risk