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Pronunciation |
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(suks
in il KOE
leen) |
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U.S. Brand
Names |
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Anectine® Chloride Injection;
Anectine®
Flo-Pack®; Quelicin®
Injection |
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Generic
Available |
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No |
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Synonyms |
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Succinylcholine Chloride; Suxamethonium Chloride |
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Pharmacological Index |
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Neuromuscular Blocker Agent, Depolarizing |
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Use |
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Produces skeletal muscle relaxation in procedures of short duration such as
endotracheal intubation or endoscopic exams |
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Pregnancy Risk
Factor |
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C |
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Contraindications |
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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 |
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Warnings/Precautions |
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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 |
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Adverse
Reactions |
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>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) |
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Overdosage/Toxicology |
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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 |
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Drug
Interactions |
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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) |
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Stability |
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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 |
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Mechanism of
Action |
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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 |
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Pharmacodynamics/Kinetics |
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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
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Usual Dosage |
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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 |
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Administration |
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May be given by rapid I.V. injection without further
dilution |
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Monitoring
Parameters |
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Cardiac monitor, blood pressure monitor, and ventilator required during
administration; temperature, serum potassium and calcium, assisted ventilator
status |
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Test
Interactions |
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potassium
(S) |
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Mental Health: Effects
on Mental Status |
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None reported |
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Mental Health:
Effects on Psychiatric
Treatment |
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MAOIs may prolong the effects of succinylcholine |
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Patient
Information |
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Refrigerate |
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Dosage Forms |
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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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