Ballicules.com

Terlipressin

TERLIVAZ

What it isV1- and V2-receptor agonist producing splanchnic vasoconstriction; hepatorenal syndrome.

Why this oneIt is the first targeted vasoconstrictor approved to reverse hepatorenal syndrome with rapid kidney decline.

What limits itSerious or fatal respiratory failure and ischemia require oxygenation screening; avoid in hypoxia and monitor sodium.

FDA-approved for

FDA label

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 dosingPopulationStartTargetMax
Hepatorenal syndrome with rapid reduction in kidney functionAdults0.85 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 baseline1.7 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

Contraindications

Cautions

Adverse reactions

Pregnancy May cause fetal harm; induces uterine contractions and endometrial ischemia

Lactation No data on presence in milk; weigh clinical need against risk

⚠ BOXED WARNING

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Terlipressin ballicule

Terlipressin ballicule: receptor binding, kinetics and half-life diagram

Open Terlipressin in the interactive console ↗