0.6 mg/kg IV (0.45 mg/kg lower option; up to 0.9-1.2 mg/kg bolus)
0.6 mg/kg IV
1.2 mg/kg IV
Rapid sequence intubation
Adults
0.6-1.2 mg/kg IV
0.6-1.2 mg/kg IV
1.2 mg/kg IV
Maintenance of neuromuscular block
Adults
0.1-0.2 mg/kg IV at 25% T1 recovery
0.1-0.2 mg/kg IV PRN
Continuous infusion maintenance
Adults
10-12 mcg/kg/min IV
4-16 mcg/kg/min IV (titrate to twitch)
Tracheal intubation
Pediatric
0.6 mg/kg IV (0.45 mg/kg option)
0.6 mg/kg IV
Renal No dosage adjustment (limited renal excretion); duration not prolonged but variable
Hepatic Use with caution; clinical duration prolonged in significant hepatic impairment; higher initial dose may be needed for RSI in ascites
Reduce infusion rate 30-50% with enflurane/isoflurane; potentiated in neuromuscular disease and hypermagnesemia; resistance with burns and chronic anticonvulsants
Instructions
IV use only; individualize dose and monitor with a peripheral nerve stimulator
Use only where intubation, mechanical ventilation, oxygen therapy, and an antagonist are immediately available
Must be accompanied by adequate anesthesia or sedation (no effect on consciousness or pain)
Do not mix with alkaline solutions (e.g., barbiturates)
For infusion, dilute to 0.5-5 mg/mL in D5W or lactated Ringer's; use within 24 h
Consider a reversal agent to prevent residual paralysis, especially in geriatric patients
Contraindications
Known hypersensitivity (e.g., anaphylaxis) to rocuronium or other neuromuscular blocking agents (cross-reactivity)
Cautions
Severe anaphylaxis; cross-reactivity among neuromuscular blocking agents
Risk of death from medication errors (accidental administration)
Requires adequate anesthesia/sedation
Residual paralysis - extubate only after sufficient recovery; higher risk in geriatric patients
Long-term ICU use: tolerance and myopathy (especially with corticosteroids)
Malignant hyperthermia reported
QTc prolongation with concomitant general anesthetics (pediatric data)
Increased pulmonary vascular resistance - caution in pulmonary hypertension/valvular disease
Profound effects in myasthenia gravis or Eaton-Lambert syndrome
Adverse reactions
Transient hypotension
Transient hypertension
Arrhythmia/tachycardia
Nausea/vomiting
Bronchospasm/wheezing
Rash, injection-site edema, pruritus
Pregnancy No drug-associated risk identified over decades of use; not recommended for rapid sequence induction in Cesarean section.
Lactation No available data.
NO BOXED WARNINGS
Principal riskNo sedation whatever — awareness under paralysis