|
|
|
Pronunciation |
|
(ter
BYOO ta
leen) |
|
|
U.S. Brand
Names |
|
Brethaire®; Brethine®;
Bricanyl® |
|
|
Generic
Available |
|
No |
|
|
Synonyms |
|
Terbutaline Sulfate |
|
|
Pharmacological Index |
|
Beta2 Agonist |
|
|
Use |
|
Bronchodilator in reversible airway obstruction and bronchial
asthma |
|
|
Pregnancy Risk
Factor |
|
B |
|
|
Contraindications |
|
Hypersensitivity to terbutaline or any component, cardiac arrhythmias
associated with tachycardia, tachycardia caused by digitalis
intoxication |
|
|
Warnings/Precautions |
|
Excessive or prolonged use may lead to tolerance; paradoxical
bronchoconstriction may occur with excessive use; if it occurs, discontinue
terbutaline immediately |
|
|
Adverse
Reactions |
|
>10%:
Central nervous system: Nervousness, restlessness
Neuromuscular & skeletal: Trembling
1% to 10%:
Cardiovascular: Tachycardia, hypertension
Central nervous system: Dizziness, drowsiness, headache, insomnia
Gastrointestinal: Xerostomia, nausea, vomiting, bad taste in mouth
Neuromuscular & skeletal: Muscle cramps, weakness
Miscellaneous: Diaphoresis
<1%: Chest pain, arrhythmias, paradoxical bronchospasm
|
|
|
Overdosage/Toxicology |
|
Symptoms of overdose include seizures, nausea, vomiting, tachycardia, cardiac
dysrhythmias, hypokalemia
In cases of overdose, supportive therapy should be instituted; prudent use of
a cardioselective beta-adrenergic blocker (eg, atenolol or metoprolol) should be
considered, keeping in mind the potential for induction of bronchoconstriction
in an asthmatic individual. Dialysis has not been shown to be of value in the
treatment of an overdose with this agent. |
|
|
Drug
Interactions |
|
Decreased effect with beta-blockers
Increased toxicity with MAO inhibitors, TCAs |
|
|
Stability |
|
Store injection at room temperature; protect from heat, light, and from
freezing; use only clear solutions |
|
|
Mechanism of
Action |
|
Relaxes bronchial smooth muscle by action on beta2-receptors with
less effect on heart rate |
|
|
Pharmacodynamics/Kinetics |
|
Onset of action: Oral: 30-45 minutes; S.C.: Within 6-15 minutes
Protein binding: 25%
Metabolism: In the liver to inactive sulfate conjugates
Bioavailability: S.C. doses are more bioavailable than oral
Half-life: 11-16 hours
Elimination: In urine |
|
|
Usual Dosage |
|
Children <12 years:
Oral: Initial: 0.05 mg/kg/dose 3 times/day, increased gradually as required;
maximum: 0.15 mg/kg/dose 3-4 times/day or a total of 5 mg/24 hours
S.C.: 0.005-0.01 mg/kg/dose to a maximum of 0.3 mg/dose every 15-20 minutes
for 3 doses
Nebulization: 0.01-0.03 mg/kg/dose every 4-6 hours
Inhalation: 1-2 inhalations every 4-6 hours
Children >12 years and Adults:
Oral:
12-15 years: 2.5 mg every 6 hours 3 times/day; not to exceed 7.5 mg in 24
hours
>15 years: 5 mg/dose every 6 hours 3 times/day; if side effects occur,
reduce dose to 2.5 mg every 6 hours; not to exceed 15 mg in 24 hours
S.C.: 0.25 mg/dose repeated in 15-30 minutes for one time only; a total dose
of 0.5 mg should not be exceeded within a 4-hour period
Nebulization: 0.01-0.03 mg/kg/dose every 4-6 hours
Inhalation: 2 inhalations every 4-6 hours; wait 1 minute between inhalations
Dosing adjustment/comments in renal impairment:
Clcr 10-50 mL/minute: Administer at 50% of normal dose
Clcr <10 mL/minute: Avoid use |
|
|
Monitoring
Parameters |
|
Serum potassium, heart rate, blood pressure, respiratory
rate |
|
|
Mental Health: Effects
on Mental Status |
|
Restlessness and nervousness are common; may cause dizziness, drowsiness, or
insomnia |
|
|
Mental Health:
Effects on Psychiatric
Treatment |
|
Concurrent use with TCAs or MAOIs may increase toxicity |
|
|
Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
No information available to require special precautions |
|
|
Dental Health:
Effects on Dental Treatment |
|
No effects or complications reported |
|
|
Patient
Information |
|
Use exactly as directed (see Administration below). Do not use more often
than recommended (excessive use may result in tolerance, overdose may result in
serious adverse effects) and do not discontinue without consulting prescriber.
Maintain adequate hydration (2-3 L/day of fluids unless instructed to restrict
fluid intake). You may experience nervousness, dizziness, or fatigue (use
caution when driving or engaging in tasks requiring alertness until response to
drug is known); or dry mouth, stomach upset (frequent small meals, frequent
mouth care, chewing gum, or sucking hard candy may help). Report unresolved GI
upset; dizziness or fatigue; vision changes; chest pain, rapid heartbeat, or
palpitations; insomnia, nervousness, or hyperactivity; muscle cramping, tremors,
or pain; unusual cough; or rash (hypersensitivity).
Administration: Self-administered inhalation: Store canister upside
down; do not freeze. Shake canister before using. Sit when using medication.
Close eyes when administering terbutaline to avoid spray getting into eyes.
Exhale slowly and completely through nose; inhale deeply through mouth while
administering aerosol. Hold breath for 1-3 seconds after inhalation. Wait at
least 1 full minute between inhalations. Wash mouthpiece between use. If more
than one inhalation medication is used, use bronchodilator first and wait 5
minutes between medications. |
|
|
Nursing
Implications |
|
Parenteral form is only for S.C. use. Before using, the inhaler must be
shaken well; assess lung sounds, pulse, and blood pressure before administration
and during peak of medication; observe patient for wheezing after
administration, if this occurs, call physician |
|
|
Dosage Forms |
|
Aerosol, oral, as sulfate: 0.2 mg/actuation (10.5 g)
Injection, as sulfate: 1 mg/mL (1 mL)
Tablet, as sulfate: 2.5 mg, 5 mg |
|
|
Extemporaneous
Preparations |
|
A 1 mg/mL suspension made from terbutaline tablets in simple syrup NF is
stable 30 days when refrigerated |
|
|
References |
|
Bohn D, Kalloghlian A, Jenkins J, et al,
"Intravenous Salbutamol in the Treatment of Status Asthmaticus in Children,"
Crit Care Med, 1984, 12(10):892-6.
Canny GJ and Levison H,
"Aerosols - Therapeutic Use and Delivery in Childhood Asthma," Ann
Allergy, 1988, 60(1):11-9.
Expert Panel Report 2,
"Guidelines for the Diagnosis and Management of Asthma," Clinical Practice
Guidelines, National Institutes of Health, National Heart, Lung, and Blood
Institute, NIH Publication No. 94-4051, April, 1997.
Fuglsang G, Pedersen S, and Borgstrom L,
"Dose-Response Relationships of I.V. Administered Terbutaline in Children With Asthma,"
J Pediatr, 1989, 114(2):315-20.
Goldenhersh N and Rachelefsky GS, "Childhood Asthma: Management," Pediatr
Rev, 1989, 10(9):259-67.
Kelly HW, McWilliams BC, Katz R, et al,
"Safety of Frequent High Dose Nebulized Terbutaline in Children With Acute Severe Asthma,"
Ann Allergy, 1990, 64(2 Pt 2):229-33.
Lee DC, "Terbutaline Sulfate Overdose," Ann Emerg Med, 1995,
26(1):107-8.
Rachelefsky GS and Siegel SC,
"Asthma in Infants and Children - Treatment of Childhood Asthma: Part II," J
Allergy Clin Immunol, 1985, 76(3):409-25.
Tipton WR and Nelson HS,
"Frequent Parenteral Terbutaline in the Treatment of Status Asthmaticus in Children,"
Ann Allergy, 1987, 58(4):252-6.
Zehner WJ Jr, Scott JM, Iannolo PM, et al,
"Terbutaline vs Albuterol for Out-of-Hospital Respiratory Distress: Randomized Double-Blind Trial,"
Acad Emerg Med, 1995, 2(8):686-91.
|
|
Copyright © 1978-2000 Lexi-Comp Inc. All Rights Reserved
| |