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.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Tracheal intubation | Adult | 0.15-0.2 mg/kg IV bolus | 0.4 mg/kg (studied) | |
| Maintenance neuromuscular blockade | Adult | 0.03 mg/kg IV bolus | ||
| Neuromuscular disease (intubation) | Adult | max initial bolus 0.02 mg/kg | 0.02 mg/kg | |
| Continuous infusion (surgical) | Adult/peds ≥2 y | 3 mcg/kg/min | 1-2 mcg/kg/min | |
| ICU mechanical ventilation | Adult | 3 mcg/kg/min | 0.5-10.2 mcg/kg/min | |
| Tracheal intubation | Infant 1-23 mo | 0.15 mg/kg IV | ||
| Tracheal intubation | Child 2-12 y | 0.1-0.15 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).
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
