Last reviewed · How we verify

Muscle Relaxant (Rocuronium)

Ostfold Hospital Trust · FDA-approved active Small molecule

Rocuronium blocks acetylcholine receptors at the neuromuscular junction, preventing muscle contraction and causing paralysis.

Rocuronium blocks acetylcholine receptors at the neuromuscular junction, preventing muscle contraction and causing paralysis. Used for Facilitation of endotracheal intubation during anesthesia induction, Maintenance of neuromuscular blockade during general anesthesia for surgical procedures.

At a glance

Generic nameMuscle Relaxant (Rocuronium)
Also known asEsmeron MSD
SponsorOstfold Hospital Trust
Drug classNon-depolarizing neuromuscular blocking agent
TargetNicotinic acetylcholine receptor (neuromuscular junction)
ModalitySmall molecule
Therapeutic areaAnesthesiology
PhaseFDA-approved

Mechanism of action

Rocuronium is a non-depolarizing neuromuscular blocking agent that competitively antagonizes acetylcholine at the nicotinic receptors on the motor end plate. By occupying these receptors, it prevents acetylcholine from binding and initiating muscle contraction, resulting in skeletal muscle paralysis. This effect is reversible and used during anesthesia to facilitate intubation and surgical procedures.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: