Suxamethonium (Succinylcholine)
Brand names: Anectine, Scoline
Suxamethonium (succinylcholine) is a depolarising neuromuscular blocking agent providing very rapid, short-lived muscle relaxation, used principally for tracheal intubation during rapid sequence induction.
Adult dose
Paediatric dose
Dose adjustments
A normal single dose may be administered to patients with renal insufficiency in the absence of hyperkalaemia. Multiples or larger doses may cause clinically significant rises in serum potassium and should not be used.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to suxamethonium or to any of the excipients
- Patients who are not fully anaesthetised — suxamethonium has no effect on the level of consciousness
- Personal or family history of malignant hyperthermia (suxamethonium is a recognised potential triggering agent)
- History of previous prolonged apnoea after suxamethonium, or atypical plasma cholinesterase
- States causing reduced plasma cholinesterase: end stage hepatic failure, acute or chronic renal failure
- Patients recovering from major trauma or severe burns (greatest hyperkalaemia risk 5 to 70 days after injury, potentially longer with delayed healing)
- Neurological deficits involving spinal cord injury, peripheral nerve injury or acute major muscle wasting (upper and/or lower motor neurone lesions); patients immobilised for prolonged periods may be at similar risk
- Pre-existing hyperkalaemia (in the absence of hyperkalaemia and neuropathy, renal failure is not a contraindication to a normal single dose, but multiple or large doses should not be used)
- Open eye injuries, or where an increase in intra-ocular pressure is undesirable, unless the expected benefit outweighs the potential risk to the eye
Side effects
- Very common: muscle fasciculation and post-operative muscle pains; increased intragastric pressure
- Common: increased intraocular pressure; bradycardia, tachycardia; skin flushing; rash; transient blood potassium increase
- Rare: arrhythmias including ventricular arrhythmias and cardiac arrest; bronchospasm, prolonged respiratory depression, apnoea; myoglobinaemia and myoglobinuria; trismus
- Very rare: anaphylactic reactions; malignant hyperthermia
- Also reported: hypertension and hypotension; excessive salivation; rhabdomyolysis
Interactions
- Cardiac glycosides (digitalis-like drugs) — patients on cardiac glycosides are at increased risk of ventricular dysrhythmias; the elderly may be especially susceptible (§4.4, cross-referring §4.5)
- Other neuromuscular blocking drugs, both depolarising and non-depolarising — higher rate of cross-sensitivity; caution where there is a history of sensitivity to neuromuscular blocking drugs (§4.4)
Clinical monograph
How it works
It binds and persistently activates nicotinic acetylcholine receptors at the motor end-plate, causing initial fasciculation followed by sustained depolarisation that prevents further muscle contraction.
Prescribing in practice
- It can trigger malignant hyperthermia and cause life-threatening hyperkalaemia (notably in burns, crush or denervation injury and prolonged immobility), so it is contraindicated in patients at risk and dantrolene must be available.
- Action is terminated by plasma cholinesterase; deficiency (including the inherited atypical variant) causes prolonged paralysis requiring continued ventilation.
- Bradycardia can occur, especially with repeated doses or in children, and pre-treatment to attenuate this may be considered.
Monitoring
Continuous airway, ventilation, cardiac rhythm and temperature monitoring are required, with vigilance for signs of malignant hyperthermia and prolonged blockade.
Counselling the patient
- Gives very rapid, short-lasting muscle relaxation to allow emergency airway control.
- Team: ensure full resuscitation, dantrolene and ventilatory support are available before use.
- A personal or family history of problems under anaesthesia should be flagged, as it may indicate increased risk.
Evidence & guidelines
Suxamethonium remains a standard rapid-onset agent for rapid sequence induction, with its hyperkalaemia and malignant hyperthermia risks documented in the SPC and anaesthetic guidance.
Reference: NICE; Difficult Airway Society (DAS) 2015; UK MH Unit Guidelines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Train-of-Four (TOF) Neuromuscular Monitoring · Neuromuscular Blockade
- MAGGIC Heart Failure Risk Score · Heart Failure
- Long QT Syndrome (Schwartz Score) · Channelopathy / Sudden Cardiac Death
- New Ballard Score — Gestational Age Assessment · Gestational Age
- MGFA Clinical Classification for Myasthenia Gravis · Neuromuscular
- Myasthenia Gravis Activities of Daily Living (MG-ADL) Scale · Neuromuscular
- Difficult Airway Algorithm (DAS) · DAS 2015; Royal College of Anaesthetists
- Major Haemorrhage Protocol · NICE NG24; UK MHP guidelines
- New-Onset Atrial Fibrillation · ESC 2020 AF Guidelines; NICE NG196
- Hypertensive Emergency · ESC/ESH 2018 Hypertension Guidelines; NICE NG136
- Bradycardia Management · Resuscitation Council UK ABCDE; ESC 2021 Pacing Guidelines
- Ventricular Tachycardia / Fibrillation · Resuscitation Council UK ACLS; ESC 2022 Ventricular Arrhythmia Guidelines
Featured in these MRCEM clinical pathways
Suxamethonium (Succinylcholine) is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.
MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.