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Cisatracurium

NIMBEX

What it isNondepolarizing muscle nicotinic-receptor antagonist cleared by Hofmann elimination; surgical and ICU paralysis.

Why this oneOrgan-independent clearance with little histamine release makes it especially useful in critically ill patients.

What limits itIts slow onset makes it unsuitable for rapid-sequence intubation. Paralysis provides no sedation or analgesia.

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Tracheal intubationAdult0.15-0.2 mg/kg IV bolus0.4 mg/kg (studied)
Maintenance neuromuscular blockadeAdult0.03 mg/kg IV bolus
Neuromuscular disease (intubation)Adultmax initial bolus 0.02 mg/kg0.02 mg/kg
Continuous infusion (surgical)Adult/peds ≥2 y3 mcg/kg/min1-2 mcg/kg/min
ICU mechanical ventilationAdult3 mcg/kg/min0.5-10.2 mcg/kg/min
Tracheal intubationInfant 1-23 mo0.15 mg/kg IV
Tracheal intubationChild 2-12 y0.1-0.15 mg/kg IV

Renal No adjustment needed (recovery profile unchanged; time to blockade ~1 min slower in end-stage renal disease)

Hepatic No adjustment needed (minor PK differences; no clinically significant change in recovery)

First maintenance bolus 40-50 min after 0.15 mg/kg initial dose (50-60 min after 0.2 mg/kg).

Instructions

Cautions

Adverse reactions

Pregnancy No human data; no maternal or fetal toxicity in animals. 10 mL multiple-dose vial contains benzyl alcohol — use a benzyl alcohol-free formulation in pregnancy.

Lactation No data on presence in human milk; 10 mL multiple-dose vial contains benzyl alcohol — consider a benzyl alcohol-free formulation.

NO BOXED WARNINGS

Principal riskNo sedation whatever; slow onset

Classes and tags

Clinical profile

Direct muscarinic antagonism0 / 4

Mechanism of action: Cisatracurium ballicule

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

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