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SABA — Bronchodilator Pregnancy: §4.6: although no teratogenic effects have been observed in animals or in patients, Bricanyl should only be administered with caution during the first trimester of pregnancy. If used in maintenance therapy for asthma and other pulmonary diseases, Bricanyl Respules should be used with caution at the end of pregnancy because of the potential tocolytic effect. Breast-feeding: terbutaline is secreted via breast milk, but effect on the infant is unlikely at therapeutic doses.

Terbutaline

Brand names: Bricanyl

Terbutaline is a short-acting beta-2 agonist (SABA) bronchodilator used for symptomatic relief of bronchospasm in asthma and other reversible airways obstruction. It is available by inhalation and as injectable and oral preparations.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 1 or 2 Respules (5 or 10 mg) nebulised; from a multidose bottle, 0.5 to 1 ml (5 to 10 mg) diluted to the required nebuliser volume with sterile physiological saline
Route: Nebulised inhalation
Frequency: 2 to 4 times daily; in acute, severe asthma additional doses may be necessary
eMC §4.2 (Bricanyl Respules 2.5 mg/ml Nebuliser Solution, emc product 868): 'In most patients, the use of terbutaline sulfate, based on the doses below, given 2-4 times daily will be sufficient to relieve bronchospasm. In acute, severe asthma, additional doses may be necessary.' MAINTENANCE CONTEXT: when used as maintenance therapy the patient should also receive optimal anti-inflammatory therapy, e.g. inhaled corticosteroids or leukotriene receptor antagonists. ELDERLY: dosage as for adults. PAEDIATRIC (weight/age bands in mg, not a per-kg dose, so not expressed in the structured paedDose field): Respules — children over 25 kg, 1 Respule (5 mg); children under 25 kg, use multidose bottles. Multidose bottles — children 0.2 to 0.5 ml (2 to 5 mg) diluted to the required nebuliser volume with sterile physiological saline, per the SPC table of undiluted solution volumes: age under 3 / average 10 kg (22 lb) = 2.0 mg = 0.2 ml; age 3 / 15 kg (33 lb) = 3.0 mg = 0.3 ml; age 6 / 20 kg (44 lb) = 4.0 mg = 0.4 ml; age 8+ / 25+ kg (55+ lb) = 5.0 mg = 0.5 ml. Verify any under-18 use against a children's formulary. HOME NEBULISER RESTRICTION (§4.2): private purchase of nebuliser devices for use at home to deliver rescue therapy for the acute treatment of asthma in children and adolescents is not recommended; only specialists in respiratory medicine should initiate and clinically manage home nebuliser use for acute asthma in children and adolescents, children should be trained in correct device use and supervised by a responsible adult, and urgent medical assistance should be sought if worsening symptoms are not relieved by rescue medicines even if there is short-term recovery. OVERUSE (§4.4): overuse of short-acting beta-agonists may mask progression of the underlying disease and contribute to deteriorating asthma control, with increased risk of severe exacerbations and mortality — patients taking more than twice a week additional 'as needed' terbutaline should be re-evaluated. Caution in thyrotoxicosis; not to be used in hypertrophic cardiomyopathy; additional blood glucose monitoring initially in diabetic patients; potentially serious hypokalaemia may result from beta2-agonist therapy, with particular caution in acute severe asthma where the risk may be augmented by hypoxia. SOURCE CAVEATS: the fetched §4.4 was cut off at the source-fetch limit and §4.5 was not captured at all. The openFDA record in this bundle is terbutaline sulfate ORAL TABLETS — a different formulation and route — and none of its figures have been used here. SUPERSEDES EARLIER HOLD: a previous draft of this page was held because the bundle then held the Bricanyl Injection SPC and had carried an obstetric tocolysis infusion regimen onto this respiratory page. The bundle has since been re-fetched to the nebuliser solution SPC; no injection or tocolysis figure appears in this draft.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to the active substance(s) or to any of the excipients listed in section 6.1 (§4.3 — this is the only contraindication in the nebuliser solution SPC)

Side effects

  • Tremor and headache (very common)
  • Tachycardia and palpitations (common)
  • Hypokalaemia (common)
  • Muscle spasms (common) — a few patients feel tense, due to effects on skeletal muscle rather than direct CNS stimulation
  • Frequency not known: hypersensitivity reactions including angioedema, bronchospasm, hypotension and collapse; lactic acidosis; sleep disorder and behavioural disturbances such as agitation and restlessness; arrhythmias (atrial fibrillation, supraventricular tachycardia, extrasystoles); myocardial ischaemia; paradoxical bronchospasm with wheezing immediately after inhalation — treat immediately with a rapid-onset bronchodilator, discontinue and initiate alternative therapy

Interactions

  • Concomitant treatments that lower potassium — §4.4 states the hypokalaemic effect of beta2-agonist therapy may be potentiated by concomitant treatments (the sentence was cut off at the source-fetch limit)
  • Other sympathomimetic agents — concomitant use is not recommended as the combined effect on the cardiovascular system may be deleterious, although this does not preclude an adrenergic-stimulant aerosol bronchodilator for relief of acute bronchospasm (US labelling for terbutaline sulfate tablets; the UK SPC §4.5 was not captured in this bundle)
  • The eMC §4.5 interaction section was not captured in this bundle — clinician to review it in the full SPC

Clinical monograph

How it works

It selectively stimulates beta-2 adrenoceptors on airway smooth muscle, raising intracellular cyclic AMP and producing rapid bronchodilatation.

Prescribing in practice

  • Increasing or excessive use signals deteriorating asthma control and the need to review and step up preventer therapy rather than simply relying on more reliever.
  • Use with caution in cardiovascular disease, hyperthyroidism and diabetes, and be alert to additive hypokalaemia with corticosteroids, theophylline and diuretics.
  • High parenteral or nebulised doses can cause tachycardia, tremor and significant hypokalaemia requiring monitoring.

Monitoring

Monitor asthma control and reliever frequency, and check serum potassium when high doses are given, especially in severe acute asthma.

Counselling the patient

  • This is a reliever for symptoms, not a preventer; seek urgent help if it is needed more often or works less well.
  • Some shakiness or a faster heartbeat after dosing is common and usually settles.

Evidence & guidelines

Terbutaline is an established SABA whose efficacy and safety profile underpin its place in UK asthma guidance alongside other short-acting bronchodilators.

Reference: MHRA Drug Safety Update (2011) Terbutaline tocolysis; BTS/SIGN Asthma Guidelines 2019; NICE NG80; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.