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Atracurium (Atracurium Besylate)

Pfizer · FDA-approved approved Small molecule Quality 68/100

Nondepolarizing skeletal muscle relaxant that competitively antagonizes acetylcholine at motor end-plate cholinergic receptors.

Atracurium besylate is a nondepolarizing skeletal muscle relaxant indicated as an adjunct to general anesthesia for endotracheal intubation and muscle relaxation during surgery or mechanical ventilation. An initial dose of 0.4 to 0.5 mg/kg produces maximum neuromuscular block within 3 to 5 minutes with good intubation conditions in 2 to 2.5 minutes. Recovery begins approximately 20 to 35 minutes after injection with 95% recovery by 60 to 70 minutes. Contraindications include hypersensitivity to atracurium or benzyl alcohol, and numerous drug interactions may enhance neuromuscular blocking effects.

At a glance

Generic nameAtracurium Besylate
SponsorPfizer
Drug classNondepolarizing skeletal muscle relaxant
TargetCholinergic receptor sites on motor end-plate
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1983

Mechanism of action

Atracurium besylate antagonizes the neuromuscular action of acetylcholine by binding competitively with cholinergic receptor sites on the motor end-plate. This antagonism is inhibited and neuromuscular block reversed by acetylcholinesterase inhibitors such as neostigmine, edrophonium, and pyridostigmine. The duration of neuromuscular block produced by atracurium is approximately one-third to one-half the duration of block by d-tubocurarine, metocurine, and pancuronium at initially equipotent doses.

Approved indications

Common side effects

Serious adverse events

Drug interactions

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions

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