Look Up > Drugs > Succinylcholine
Succinylcholine
Pronunciation
U.S. Brand Names
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Stability
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Administration
Monitoring Parameters
Test Interactions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Patient Information
Dosage Forms

Pronunciation
(suks in il KOE leen)

U.S. Brand Names
Anectine® Chloride Injection; Anectine® Flo-Pack®; Quelicin® Injection

Generic Available

No


Synonyms
Succinylcholine Chloride; Suxamethonium Chloride

Pharmacological Index

Neuromuscular Blocker Agent, Depolarizing


Use

Produces skeletal muscle relaxation in procedures of short duration such as endotracheal intubation or endoscopic exams


Pregnancy Risk Factor

C


Contraindications

Malignant hyperthermia, myopathies associated with elevated serum creatine phosphokinase (CPK) values, narrow-angle glaucoma, hyperkalemia, penetrating eye injuries, disorders of plasma pseudocholinesterase, hypersensitivity to succinylcholine or any component


Warnings/Precautions

Use in pediatrics and adolescents; use with caution in patients with pre-existing hyperkalemia, paraplegia, extensive or severe burns, extensive denervation of skeletal muscle because of disease or injury to the CNS or with degenerative or dystrophic neuromuscular disease; may increase vagal tone


Adverse Reactions

>10%:

Ocular: Increased intraocular pressure

Miscellaneous: Postoperative stiffness

1% to 10%:

Cardiovascular: Bradycardia, hypotension, cardiac arrhythmias, tachycardia

Gastrointestinal: Intragastric pressure, salivation

<1%: Hypertension, rash, itching, erythema, hyperkalemia, myalgia, myoglobinuria, apnea, bronchospasm, circulatory collapse, malignant hyperthermia

Causes of prolonged neuromuscular blockade:

Excessive drug administration

Cumulative drug effect, decreased metabolism/excretion (hepatic and/or renal impairment)

Accumulation of active metabolites

Electrolyte imbalance (hypokalemia, hypocalcemia, hypermagnesemia, hypernatremia)

Hypothermia

Drug interactions

Increased sensitivity to muscle relaxants (eg, neuromuscular disorders such as myasthenia gravis or polymyositis)


Overdosage/Toxicology

Symptoms of overdose include respiratory paralysis, cardiac arrest

Bradyarrhythmias can often be treated with atropine 0.1 mg (infants); do not treat with anticholinesterase drugs (eg, neostigmine, physostigmine) since this may worsen its toxicity by interfering with its metabolism


Drug Interactions

Increased toxicity: Anticholinesterase drugs (neostigmine, physostigmine, or pyridostigmine) in combination with succinylcholine can cause cardiorespiratory collapse; cyclophosphamide, oral contraceptives, lidocaine, thiotepa, pancuronium, lithium, magnesium salts, aprotinin, chloroquine, metoclopramide, terbutaline, and procaine enhance and prolong the effects of succinylcholine

Prolonged neuromuscular blockade:

Inhaled anesthetics

Local anesthetics

Calcium channel blockers

Antiarrhythmics (eg, quinidine or procainamide)

Antibiotics (eg, aminoglycosides, tetracyclines, vancomycin, clindamycin)

Immunosuppressants (eg, cyclosporine)


Stability

Refrigerate (2°C to 8°C/36°F to 46°F); however, remains stable for 14 days unrefrigerated; powder form does not require refrigeration

Stability of parenteral admixture at refrigeration temperature (4°C): 24 hours in D5W or NS

I.V. form is incompatible when mixed with sodium bicarbonate, pentobarbital, thiopental


Mechanism of Action

Acts similar to acetylcholine, produces depolarization of the motor endplate at the myoneural junction which causes sustained flaccid skeletal muscle paralysis produced by state of accommodation that developes in adjacent excitable muscle membranes


Pharmacodynamics/Kinetics

Onset of effect: I.M.: 2-3 minutes; I.V.: Complete muscular relaxation occurs within 30-60 seconds of injection

Duration: I.M.: 10-30 minutes; I.V.: 4-6 minutes with single administration

Metabolism: Rapidly hydrolyzed by plasma pseudocholinesterase


Usual Dosage

I.M., I.V.:

Older Children and Adolescents: Intermittent: Initial: 1 mg/kg/dose one time; maintenance: 0.3-0.6 mg/kg every 5-10 minutes as needed

Adults: 0.6 mg/kg (range: 0.3-1.1 mg/kg) over 10-30 seconds, up to 150 mg total dose

Maintenance: 0.04-0.07 mg/kg every 5-10 minutes as needed

Continuous infusion: 2.5 mg/minute (or 0.5-10 mg/minute); dilute to concentration of 1-2 mg/mL in D5W or NS

Note: Pretreatment with atropine may reduce occurrence of bradycardia

Dosing adjustment in hepatic impairment: Dose should be decreased in patients with severe liver disease


Administration

May be given by rapid I.V. injection without further dilution


Monitoring Parameters

Cardiac monitor, blood pressure monitor, and ventilator required during administration; temperature, serum potassium and calcium, assisted ventilator status


Test Interactions

potassium (S)


Mental Health: Effects on Mental Status

None reported


Mental Health: Effects on Psychiatric Treatment

MAOIs may prolong the effects of succinylcholine


Patient Information

Refrigerate


Dosage Forms

Injection, as chloride: 20 mg/mL (10 mL); 50 mg/mL (10 mL); 100 mg/mL (5 mL, 10 mL, 20 mL)

Powder for injection, as chloride: 100 mg, 500 mg, 1 g


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