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Formoterol

Long-acting beta-2 agonist (LABA) · Bronchodilator

Also known as Formoterol Fumarate, Foradil, Oxis

START
Always prescribe with ICS for asthma; 4.5-12 mcg BD via inhaler; check baseline heart rate, BP, K+; provide asthma action plan
TYPICAL MAX
24 mcg BD; 40 mcg/day total
STOP IF
Paradoxical bronchospasm, significant arrhythmia, inadequate asthma control (step up therapy), severe hypokalemia
WATCH
Asthma control (ACT score), heart rate, BP, K+ (if on diuretics), inhaler technique, ensure concurrent ICS use
CDSCO approvedSchedule HATC R03AC13
Dose laddermg/d
0.005start0.012titrate0.024ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo renal adjustment needed090

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
3minONSET45minPEAK9h12hDURATION
ONSET
3min · 1-3 minutes (rapid for LABA)
PEAK
45min · 0.5-1 hour
9h · 8-10 hours
DURATION
12h · 12-hour bronchodilation
EXCRETION
Renal (metabolites)
route + CYP
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Compatible with pregnancy; asthma control benefits outweigh risks; use with ICS
FDA category + note
Top interactionssee all 12
  • MoclobemideSevereTextbookG&G 14e · p264
  • CarteololSevereDatabaseDDInter
  • CarvedilolSevereDatabaseDDInter
  • LabetalolSevereDatabaseDDInter
Available in India

3 branded formulations and 238 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Mechanism

Selective agonist at beta-2 adrenergic receptors on airway smooth muscle, activating adenylate cyclase and increasing intracellular cAMP, leading to smooth muscle relaxation and bronchodilation. Rapid onset of action with sustained 12-hour duration. Also inhibits mast cell mediator release and increases mucociliary clearance.

Indications

Asthma - maintenance treatment (in combination with ICS, NEVER monotherapy)COPD - maintenance bronchodilation (as monotherapy or combination)Exercise-induced bronchospasm preventionChronic bronchitis, emphysema

Dosing

Adult
Inhalation: 4.5-24 mcg BD (depending on device). DPI (Foradil): 12 mcg BD. MDI (Atimos): 12 mcg BD. Neb: 20 mcg BD
Pediatric
6-17 years: 4.5-12 mcg BD (asthma, with ICS). <6 years: limited data
Renal adjustment
No adjustment needed
Hepatic adjustment
No adjustment needed; minimal hepatic metabolism
Geriatric
Standard dosing; monitor for cardiovascular effects
Max dose
24 mcg BD (inhalation); 40 mcg/day total

Pharmacokinetics

Onset
1-3 minutes (rapid onset for LABA)
Peak effect
Inhalation: 0.5-1 hour
Duration
12 hours
Half-life
8-10 hours
Bioavailability
Inhalation: ~8% (systemic from lung); Oral swallowed: ~65% (extensive first-pass)
Protein binding
46-58%
Metabolism
Hepatic CYP2D6 and CYP2C19 (O-demethylation and glucuronidation)
Excretion
Renal (majority, as metabolites); fecal (~10%)

Contraindications

  • Hypersensitivity to formoterol
  • Asthma monotherapy without ICS (black box warning - increased mortality risk)
  • Severe cardiovascular disease (unstable angina, recent MI)
  • Tachyarrhythmias
  • Untreated hypokalemia

Side effects

Common
TremorPalpitationsTachycardiaHeadacheMuscle crampsHypokalemiaThroat irritation
Serious
  • Paradoxical bronchospasm
  • Cardiovascular events (arrhythmias, angina, MI)
  • Hypokalemia (potentially severe)
  • Hyperglycemia
  • Anaphylaxis (rare)

Pregnancy & lactation

Pregnancy

Compatible with pregnancy; asthma control benefits outweigh risks; use with ICS

Lactation

Excretion in breast milk unknown; likely compatible at standard doses

Drug interactions

Moclobemide
Severe
Textbook

Increased risk of adverse cardiovascular effects.

At least 2 weeks should elapse between the use of MAO inhibitors and administration of β2 agonists or other sympathomimetics.

Source: G&G 14e · p264

Carteolol
Severe
Database

Drug interaction classified as: antagonism

Source: DDInter

Carvedilol
Severe
Database

Drug interaction classified as: antagonism.

Source: DDInter

Labetalol
Severe
Database

Clinical effect not specified

Source: DDInter

Levobunolol
Severe
Database

Clinical effect not specified

Source: DDInter

Macimorelin
Severe
Database

Clinical effect not specified

Source: DDInter

Metipranolol
Severe
Database

Clinical effect not specified

Source: DDInter

Nadolol
Severe
Database

Clinical effect not specified

Source: DDInter

Ozanimod
Severe
Database

Clinical effect not specified

Source: DDInter

Penbutolol
Severe
Database

Clinical effect not specified

Source: DDInter

Pindolol
Severe
Database

Clinical effect not specified

Source: DDInter

Propranolol
Severe
Database

.

Source: DDInter

Related guidelines

Ask House about Formoterol

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19