Succinylcholine (Suxamethonium Chloride)
- Atc Codes:M03AB01
- CAS Codes:71-27-2#6101-15-1
- PHARMGKB ID:71-27-2#6101-15-1
Table of contents
- Brand Names
- Chemistry
- Pharmacologic Category
- Mechanism of Action
- Therapeutic Use
- Pregnancy and Lactation Implications
- Contraindications
- Warnings and Precautions
- Adverse Reactions
- Caution and personalized dose adjustment in patients with the following genotypes
- Other genes that may be involved
- Substrate of
- Drug Interactions
- Dosage
- Pharmacokinetics and Pharmacodynamics
- Special Considerations
Brand Names
Europe
Austria: Lysthenon; Belgium: Myoplegine; Bulgaria: Lysthenon; Estonia: Lysthenon; Finland: Sukolin; France: Celocurine; Germany: Lysthenon, Pantolax, Succinyl-Asta, Succinylcholin; Greece: Lycitrope, Mioflex; Ireland: Anectine, Suxamethonium Chloride; Italy: Midarine, Succinil; Latvia: Lysthenon; Lithuania: Lysthenon; Luxembourg: Myoplegine, Succinyl-Asta; Malta: Anectine; Netherlands: Curalest, Suxamethoniumchloride; Poland: Chlorsuccillin; Portugal: Mioflex, Suxametónio; Romania: Lysthenon; Slovakia: Lysthenon, Succinylcholinjodid; Spain: Anectine, Mioflex; Sweden: Celocurin; UK: Anectine, Suxamethonium Chloride.
North America
Canada: Quelicin, Succinylcholine Chloride; USA: Anectine, Quelicin.
Latin America
Argentina: Actirelax, Fosfitone, Succi, Succinilcolina; Brazil: Quelicin, Succitrat, Succnil Colin; Mexico: Anectine.
Asia
Japan: Succin, Relaxin.
Drug combinations
Chemistry
Succinylcholine Chloride: C~14~H~30~Cl~2~N~2~O~4~. Mw: 361.31. (1) Ethanaminium, 2,2′-[(1,4-dioxo-1,4-butanediyl)bis(oxy)]bis[N,N,N-trimethyl-], dichloride; (2) Choline chloride succinate (2:1). CAS-71-27-2; CAS-6101-15-1 (dihydrate).
Pharmacologic Category
Skeletal Muscle Relaxants; Neuromuscular Blocking Agents, Depolarizing. (ATC-Code: M03AB01).
Mechanism of action
Produces skeletal muscle relaxation by causing decreased response to acetylcholine (ACh) at myoneural (neuromuscular) junction of skeletal muscle. Exhibits high affinity for ACh receptor sites and produces depolarization of motor end-plate at myoneural junction, resulting in transient twitching or fasciculation of skeletal muscles, followed by muscle paralysis. Stimulates cardiac vagus and subsequently sympathetic ganglia.
Therapeutic use
Adjunct to general anesthesia to facilitate both rapid sequence and routine endotracheal intubation and to relax skeletal muscles during surgery. To reduce intensity of muscle contractions of pharmacologically- or electrically-induced convulsions.
Pregnancy and lactiation implications
Reproduction studies not conducted. Small amounts cross placenta. Sensitivity to succinylcholine may be increased due to ~24% decrease in plasma cholinesterase activity during pregnancy and several days postpartum. Excretion in breast milk unknown (use with caution in nursing women).
Unlabeled use
Contraindications
Hypersensitivity to succinylcholine or any component of the formulation. Personal or familial history of malignant hyperthermia. Myopathies associated with elevated serum creatine phosphokinase values. Acute phase of injury following major burns, multiple trauma, extensive denervation of skeletal muscle or upper motor neuron injury.
Warnings and precautions
Risk of bradycardia may be increased with second dose and may occur more in children (occurrence may be reduced by pre-treating with atropine). May increase intraocular pressure (caution with narrow-angle glaucoma or penetrating eye injuries). Use may be associated with acute onset of malignant hyperthermia (higher risk if concomitant administration of volatile anesthetics). May increase vagal tone. Use with caution in extensive or severe burns (risk of hyperkalemia). Alkalosis, hypercalcemia, demyelinating lesions, peripheral neuropathies, denervation, infection, muscle trauma, and diabetes mellitus may result in antagonism of neuromuscular blockade. Electrolyte abnormalities, severe hyponatremia, severe hypocalcemia, severe hypokalemia, hypermagnesemia, neuromuscular diseases, acidosis, acute intermittent porphyria, Eaton-Lambert syndrome, myasthenia gravis, renal failure, and hepatic failure may result in potentiation of neuromuscular blockade. Use with caution in patients suspected of being homozygous for the atypical plasma cholinesterase gene. Plasma cholinesterase activity may also be reduced by burns, decompensated heart disease, infections, malignant tumors, myxedema, pregnancy, severe hepatic or renal dysfunction, ulcer, and certain medications and chemicals. Use with caution in the elderly; effects and duration are more variable. Acute rhabdomyolysis with hyperkalemia, ventricular arrhythmias and cardiac arrest reported (rarely) in children with undiagnosed skeletal muscle myopathy (use in children should be reserved for emergency intubation or where immediate airway control is necessary). Maintenance of an adequate airway and respiratory support is critical.