Formoterol: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
Formoterol: clinical details
Prescribing considerations
- In asthma, use only as add-on therapy to adequate inhaled corticosteroid treatment; it is not sufficient as initial or sole therapy.
- Do not initiate during an acute severe exacerbation or significantly worsening asthma.
- Reassess control, adherence and inhaler technique if symptoms persist, deteriorate or use increases.
- Use cautiously with QT prolongation, thyrotoxicosis, phaeochromocytoma, severe hypertension, significant structural heart disease, tachyarrhythmia or severe heart failure.
- Pharmacokinetic data are unavailable in renal or hepatic impairment; exposure may rise in severe liver cirrhosis.
Contraindications and cautions
- Hypersensitivity to formoterol or an excipient.
- Because the selected powder contains lactose, it should not be used in rare hereditary galactose intolerance, total lactase deficiency or glucose-galactose malabsorption.
- The selected product is not recommended below 6 years because safety and efficacy data are insufficient.
Monitoring
- Clinical response, exacerbations, nocturnal symptoms and changing reliance on bronchodilator treatment.
- Inhaler technique and continued inhaled corticosteroid use in asthma.
- Serum potassium during acute severe asthma or when hypoxia or potassium-lowering medicines increase risk.
- Blood glucose initially in people with diabetes.
- Heart rate, rhythm and relevant cardiovascular symptoms in susceptible patients.
Clinical pharmacology
Formoterol is a selective beta2-adrenoceptor agonist that rapidly relaxes bronchial smooth muscle. After inhalation it is rapidly absorbed and mainly cleared through metabolism, including glucuronidation and O-demethylation.
Formulation and product differences
- The selected product is a multidose, inspiratory-flow-driven dry-powder Turbohaler rather than a pressurised aerosol.
- It contains lactose monohydrate with small amounts of milk protein, which may cause allergic reactions.
- The small quantity of powder means patients may neither taste nor feel delivery.
- Other products include different dry-powder devices, aerosols and combination inhalers; device technique and accompanying active ingredients are not interchangeable.
Formoterol preparations and strengths
Inhaled preparation
Route: Inhaled
Strengths: 12 micrograms/actuation, 12 micrograms/dose
Formoterol interactions
Tell the prescriber or pharmacist about all medicines, including eye drops and non-prescription products. Important examples include:
Beta blockers, including timolol eye drops
May weaken or block formoterol's airway-opening effect and provoke bronchospasm.
Other beta2 agonists, sympathomimetics or ephedrine
Can increase effects such as tremor, palpitations and a fast heartbeat.
Theophylline, systemic corticosteroids and loop or thiazide diuretics
May increase the risk of low blood potassium.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.