Cisatracurium is a skeletal muscle relaxant used to facilitate tracheal intubation, muscle relaxation in surgery, or mechanical ventilation. Nimbex. Generic Name Cisatracurium DrugBank Accession Number DB00565 Background. Cisatracurium besylate is a bisquaternary benzylisoquinolinium stereoisomer of atracurium with intermediate onset and duration of neuromuscular blockade. It produces predictable, dose-dependent nondepolarizing blockade after intravenous administration, with clinical onset typically within 2 to 3 minutes and recovery in roughly 30 to 90 minutes depending on dose and monitoring methods. Elimination is largely organ independent via Hofmann elimination and ester hydrolysis, yielding degradation products including a monoquaternary acrylate intermediate and the tertiary amine metabolite laudanosine; because clearance does not depend on renal or hepatic function to the same extent as many other neuromuscular blockers, cisatracurium is preferred in patients with organ impairment. Pharmacodynamically it has a lower propensity for histamine release than atracurium and is monitored using peripheral nerve stimulation and quantitative neuromuscular transmission techniques for dose titration and reversal decisions.

Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium / Atracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
Parent: Cisatracurium
The principal related compounds and degradation products associated with cisatracurium are other stereoisomeric components from the atracurium mixture, the monoquaternary acrylate intermediate formed during Hofmann elimination, and the tertiary amine metabolite laudanosine; trace levels of related synthetic impurities from manufacture may also be present. Typical quality specifications used in industry and pharmacopeial monographs target very low amounts of related substances at release, for example individual known or unknown impurities generally controlled at low parts per hundred or parts per thousand levels; manufacturers commonly set limits such that single related substances are below approximately 0.2 to 0.5 percent and total related substances are below approximately 1.0 to 1.5 percent in the drug substance, while laudanosine in the finished drug product at release is often at or below about 0.05 to 0.1 percent. Actual acceptance criteria and analytical limits vary by manufacturer and regulatory monograph, and stability testing tracks increases in Hofmann elimination products under elevated temperature or pH to establish shelf life and storage conditions.
Cisatracurium is used to produce neuromuscular blockade to facilitate tracheal intubation, provide skeletal muscle relaxation during surgical procedures, and enable controlled mechanical ventilation in intensive care settings.
Cisatracurium is one of the stereoisomers of atracurium selected for clinical use because it provides similar intermediate-duration nondepolarizing blockade with less histamine release and more predictable pharmacokinetics; both undergo Hofmann elimination, but cisatracurium typically requires lower doses and yields fewer adverse hemodynamic effects.
Cisatracurium is a neuromuscular blocker that causes reversible skeletal muscle paralysis for the purpose of intubation and surgical relaxation; it is a pharmacologic paralytic used under controlled clinical conditions with airway and respiratory support available.
The common brand name for cisatracurium is Nimbex.