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Terbutaline
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
Monitoring Parameters
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Nursing Implications
Dosage Forms
Extemporaneous Preparations
References

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.


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