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Neuromuscular Blocker Pregnancy: Should not be administered to pregnant women unless the expected benefit outweighs possible risks to the foetus; in normal therapeutic doses it does not cross the placental barrier in sufficient amounts to affect the respiration of the infant, and the benefits of use as part of a rapid sequence induction normally outweigh the possible risk. Plasma cholinesterase falls during the first trimester and further after delivery, so a high proportion of pregnant and puerperal patients may exhibit mildly prolonged neuromuscular blockade. Breast-feeding: it is not known whether suxamethonium or its metabolites are excreted in human milk — caution should be exercised.

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.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 1 mg/kg intravenously to achieve endotracheal intubation (usually produces muscular relaxation in about 30 to 60 seconds, with a duration of action of about 2 to 6 minutes)
Route: Intravenous bolus injection (usual method); may also be given by intramuscular bolus injection or by intravenous infusion
Frequency: Single dose for intubation; supplementary doses of 50% to 100% of the initial dose at 5 to 10 minute intervals will maintain muscle relaxation during short surgical procedures performed under general anaesthesia
Max: The total dose given by repeated intravenous injection or continuous infusion should not exceed 500 mg per hour
Dose depends on body weight, degree of muscular relaxation required, route of administration and individual response. Larger doses produce more prolonged relaxation, but doubling the dose does not necessarily double the duration. PROLONGED PROCEDURES — intravenous infusion as a 0.1% to 0.2% solution, diluted in 5% glucose solution or sterile isotonic saline solution, at a rate of 2.5 to 4 mg per minute, adjusted according to individual response. Monitoring of neuromuscular function is recommended during infusion or when relatively large cumulative doses are given over a short period. ELDERLY — dosage requirements comparable to younger adults; the elderly may be more susceptible to cardiac arrhythmias, especially if digitalis-like drugs are also being taken. REDUCED PLASMA CHOLINESTERASE — prolonged and intensified neuromuscular blockade may occur; it may be advisable to administer reduced dosages. HEPATIC IMPAIRMENT — plasma cholinesterase levels often fall in liver disease but are seldom low enough to significantly prolong suxamethonium-induced apnoea. Suxamethonium paralyses respiratory muscles and has no effect on consciousness; administer only by or under close supervision of an anaesthetist, with facilities for immediate endotracheal intubation and intermittent positive pressure ventilation. Pre-treatment with intravenous atropine or glycopyrrolate can significantly reduce suxamethonium-related bradycardia. NOTE ON SOURCES: §4.5 was not captured in the fetched bundle — the interactions listed are taken from the §4.3/§4.4 text that was captured; clinician to check the full §4.5.

Paediatric dose

Route: Intravenous (intramuscular alternative — see notes)
Frequency: Single dose for intubation; when given as intravenous infusion in children the dosage is as for adults with a proportionately lower initial infusion rate based on body weight
Max: A total dose of 150 mg should not be exceeded (stated for the intramuscular route)
The SPC gives two age-band intravenous doses, so no single per-kg value can be entered: 'The recommended intravenous dose of Suxamethonium for neonates and infants is 2 mg/kg. A dose of 1 mg/kg in older children is recommended.' Infants and young children are more resistant to suxamethonium compared with adults. INTRAMUSCULAR: 'Suxamethonium may be given intramuscularly to infants at doses up to 4 to 5 mg/kg and in older children up to 4 mg/kg. These doses produce muscular relaxation within about 3 minutes. A total dose of 150 mg should not be exceeded.' Bradycardias are more commonly observed in children. There are case reports of hyperkalaemia-related cardiac arrest following suxamethonium in patients with congenital cerebral palsy, tetanus, Duchenne muscular dystrophy and closed head injury, and rarely in children with hitherto undiagnosed muscular disorders. Verify against a children's formulary before use.

Dose adjustments

Renal

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.

📚 MRCEM Revision

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.