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Albuterol Sulfate
Albuterol Sulfate
Pregnancy Category C
Drug classes
Sympathomimetic
Beta 2-selective adrenergic agonist
Bronchodilator
Antasthmatic
Therapeutic actions
In low doses, acts relatively selectively at beta2-adrenergic receptors to cause
bronchodilation and vasodilation; at higher doses, beta2 selectivity is lost, and the
drug acts at beta2 receptors to cause typical sympathomimetic cardiac effects.
Indications
Relief and prevention of bronchospasm in patients with reversible obstructive
airway disease
Inhalation: Treatment of acute attacks of bronchospasm
Prevention of exercise-induced bronchospasm
Unlabeled use: Adjunct in treating serious hyperkalemia in dialysis patients;
seems to lower potassium concentrations when inhaled by patients on
hemodialysis
Dosages
ADULTS
Oral
Initially, 2 or 4 mg (1–2 tsp syrup) tid–qid PO; may cautiously increase dosage if
necessary to 4 or 8 mg qid, not to exceed 32 mg/day.
Inhalation
One 200 mcg capsule q 4–6 hr up to two 200 mcg capsules q 4–6 hr.
o Prevention of exercise-induced asthma: One 200 mcg capsule inhaled
15 min before exercise.
PEDIATRIC PATIENTS
Oral, tablets
2–12 yr: For child 10–15 kg, use 1.25 mg; for child > 15 kg, use 2.5 mg.
12 yr: Use adult dosage.
Solution for inhalation
Adverse effects
CNS: Restlessness, apprehension, anxiety, fear, CNS stimulation, hyperkinesia,
insomnia, tremor, drowsiness, irritability, weakness, vertigo, headache
CV: Cardiac arrhythmias, tachycardia, palpitations, PVCs (rare), anginal pain
Dermatologic: Sweating, pallor, flushing
GI: Nausea, vomiting, heartburn, unusual or bad taste in mouth
GU: Increased incidence of leiomyomas of uterus when given in higher than
human doses in preclinical studies
Respiratory: Respiratory difficulties, pulmonary edema, coughing, bronchospasm,
paradoxical airway resistance with repeated, excessive use of inhalation
preparations
Nursing considerations
Assessment
History: Hypersensitivity to albuterol; tachyarrhythmias, tachycardia caused
by digitalisintoxication; general anesthesia with halogenated hydrocarbons or
cyclopropane; unstable vasomotor system disorders; hypertension; coronary
insufficiency, CAD; history of CVA; COPD patients who have developed
degenerative heart disease; diabetes mellitus; hyperthyroidism; history of seizure
disorders; psychoneurotic individuals; lactation
Physical: Weight; skin color, T, turgor; orientation, reflexes, affect; P, BP; R,
adventitious sounds; blood and urine glucose, serum electrolytes, thyroid function
tests, ECG
Interventions
Use minimal doses for minimal periods; drug tolerance can occur with prolonged
use.
Maintain a beta-adrenergic blocker (cardioselective beta-blocker, such as
atenolol, should be used with respiratory distress) on standby in case cardiac
arrhythmias occur.
Prepare solution for inhalation by diluting 0.5 mL 0.5% solution with 2.5 mL
normal saline; deliver over 5–15 min by nebulization.
Do not exceed recommended dosage; administer pressurized inhalation drug
forms during second half of inspiration, because the airways are open wider and
the aerosol distribution is more extensive.
Teaching points
Do not exceed recommended dosage; adverse effects or loss of effectiveness
may result. Read the instructions that come with respiratory inhalant.
You may experience these side effects: Dizziness, drowsiness, fatigue, headache
(use caution if driving or performing tasks that require alertness); nausea,
vomiting, change in taste (eat frequent small meals); rapid heart rate, anxiety,
sweating, flushing, insomnia.
Report chest pain, dizziness, insomnia, weakness, tremors or irregular heartbeat,
difficulty breathing, productive cough, failure to respond to usual dosage