Terbutaline is a beta2-adrenergic agonist used mainly for relief of reversible bronchoconstriction. Veterinary applications include feline asthma and selected canine or equine airway disorders with a bronchospastic component. Injectable preparations provide an option for selected acute episodes, while oral use and clinical response differ substantially among species.
Group
Beta2-adrenergic bronchodilator
Mechanism of Action
Terbutaline activates beta2 receptors coupled to stimulatory G proteins, increasing adenylyl cyclase activity and cyclic AMP. Downstream signaling reduces airway smooth-muscle contraction and produces bronchodilation. Additional beta-adrenergic effects can influence cellular potassium uptake and smooth muscle at other sites. Its primary respiratory effect is relaxation of bronchial muscle rather than suppression of the underlying airway inflammation.
Dose Rates
Dogs
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Bronchoconstriction | 1.25–5 mg/animal | PO | Every 8 h | |
| Acute bronchoconstriction | 3–5 mcg/kg | SC | Every 4–6 h | Usually one emergency dose; repeat only if necessary. |
| Tracheal collapse or expiratory dyspnea | 1.25–5 mg/animal | PO | Every 8–12 h | |
| Bradyarrhythmia adjunct | 0.2 mg/kg | PO | Every 8–12 h | Benefit often partial or temporary. |
| Premature labor suppression | 0.03 mg/kg | PO, SC | Every 8 h | Stop 48 hours before calculated delivery date to permit normal labor. |
| Acute tracheal collapse bronchodilation | 0.01 mg/kg | IV, IM, SC |
Cats
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Bronchoconstriction | 0.1 mg/kg | PO | Every 8 h | |
| Bronchoconstriction | 0.625 mg/animal | PO | Every 12 h | |
| Acute bronchoconstriction | 5–10 mcg/kg | SC, IM | Every 4 h | |
| Acute bronchoconstriction | 0.05 mg/animal | SC | Common fixed feline amount. | |
| Acute bronchoconstriction | 0.01 mg/kg | IV, SC, IM | ||
| Feline asthma maintenance | 0.312–0.625 mg/animal | PO | Every 8–12 h | Larger cats have received up to 1.25 mg; titrate to effect. |
| Bradyarrhythmia adjunct | 0.625 mg/animal | PO | Every 8–12 h |
Horses
| Use / stage | Dose | Route | Schedule | Instructions |
|---|---|---|---|---|
| Equine asthma bronchoconstriction | 2–5 mcg/kg | IV | Every 6–8 h | Or as needed; oral absorption is poor. |
| Reported terbutaline therapy | 0.0033 mg/kg | IV |
Indications
- Relief of acute bronchospasm in cats with asthma.
- Adjunctive bronchodilation in selected cats or dogs with reversible airway obstruction associated with asthma or bronchitis.
- Short-term relief of bronchoconstriction in selected horses with equine asthma using a supported parenteral regimen.
Contraindications
- Cardiac disease or tachyarrhythmia risk
- Late gestation unless suppression of uterine contractions is intended
Interactions
- Other cardiac stimulants increase adverse effects.
Adverse effects
- Tachycardia, tremor, arrhythmias, hypokalemia and hyperglycemia.
Toxicity
Excess beta stimulation can cause marked hypokalemia; potassium replacement must be controlled by measured concentrations and ECG. Excess beta stimulation can cause arrhythmias, tremor, hyperthermia and electrolyte shifts. ECG and potassium monitoring guide treatment; beta blockade may worsen bronchoconstriction.
Preparations
| Preparation | Form | Strength | Route |
|---|---|---|---|
| Terbutaline 2.5 mg | Tablet | 2.5 mg / tablet | PO |
| Terbutaline 5 mg | Tablet | 5 mg / tablet | PO |
| Terbutaline sulfate injection 1 mg/mL | Injection | 1 mg / mL | SC, IM, IV |
Monitoring and Administration
Monitor pulse and potassium with high exposure. Oxygen and anti-inflammatory treatment may also be needed during bronchospasm.
Discard darkened injection; reported syrup suspensions remained stable for 55 days.
Size-based canine chronic-airway alternatives give 0.625-1.25 mg small, 1.25-2.5 mg medium, or 2.5-5 mg large dogs every 12 hours without numerical size boundaries. Equine quantitative intradermal sweat testing uses serial dilution and local response measurements; intradermal route is not a systemic bronchodilator dose.