Bedside Snapshot

Use It For
Acute bronchospasm in asthma or COPD exacerbation; adjunct for bronchospasm in anaphylaxis, after IM epinephrine; hyperkalemia (adjunct, off-label); prevention of exercise-induced bronchospasm
Adult Dose
  • Asthma (EPR-3): 2.5–5 mg nebulized every 20 min ×3, or 4–8 puffs MDI; GINA 2026 stricter
  • Severe: 10–15 mg/hr continuous
  • Hyperkalemia: 10–20 mg neb, add-on to insulin
  • Differs from FDA label: 2.5 mg neb 3–4×/day; 2 puffs MDI
Pediatric Dose
Age 2 yr and older: 2.5 mg nebulized (mild) or 5 mg nebulized / 6 puffs MDI (distress). Under 2 yr: not covered; no bronchiolitis. Differs from FDA label: label is 2.5 mg 3–4 times daily (ages 2–12); 5 mg is off-label.
Onset / Duration
INH (MDI or nebulized): ~5 min / 3–6 hr, peak ~1 hr (children 4–11 yr, MDI: ~8 min, peak ~1.5 hr). K⁺ lowering: within 30 min / at least 2 hr
Do Not Give / Hold If
Albuterol or component allergy (DPI: severe milk-protein allergy); worse wheeze right after a dose; new chest pain, ischemic ST change or tachyarrhythmia
Watch For
Tachyarrhythmia (ECG); hypokalemia (K⁺); lactic acidosis at high doses (lactate, tachypnea despite better air entry); paradoxical bronchospasm
Reversal / Rescue
No antidote: stop dosing, check K⁺ and ECG, supportive care; a cardioselective β-blocker may be considered for tachyarrhythmia, bearing in mind bronchospasm risk (label)
Must Remember
Toxicity mimics failure: tachycardia, hypokalemia and lactic acidosis after high doses look like worsening asthma. Reassess before stacking more, and treat a silent chest as near-arrest.

Indications

Emergency & Prehospital

  • Acute asthma exacerbation: start here at every severity. For moderate to severe attacks, add ipratropium
  • Chronic obstructive pulmonary disease (COPD) exacerbation: start with a bronchodilator. A short-acting anticholinergic can join it or stay out
  • Bronchospasm with anaphylaxis: the adjunct for bronchospasm only, and only after IM epinephrine (GINA 2026; NASEMSO v3.0, Anaphylaxis, p. 66). It does not treat airway edema or shock.
  • Other reversible bronchospasm: labeled for reversible obstructive airway disease in adults and children

ED / ICU / Transport

  • Severe or life-threatening asthma: keep nebulizing, repeated or continuous, while systemic corticosteroids and IV magnesium get to work
  • Hyperkalemia (off-label): This buys time. Albuterol shifts K⁺ into the cells. It does not remove K⁺. It works best paired with IV insulin and glucose, since the pair lowers K⁺ more than insulin alone, so use that pairing wherever you can. The UK Kidney Association recommends it at K⁺ ≥6.5 mEq/L and calls it optional at 6.0–6.4. It advises against albuterol alone in severe hyperkalemia, because response varies. Up to 40% of patients with end-stage renal disease do not respond. No insulin-glucose? Albuterol is only a bridge. Arrange K⁺ removal.
  • Hyperkalemic cardiac arrest: AHA 2025 Part 10 rates inhaled β2-agonists COR 3: No Benefit (C-EO). Keep albuterol out of arrest care.

Other Uses

  • Prevention of exercise-induced bronchospasm: labeled for age 4 yr and older
  • As-needed reliever in chronic asthma or COPD: the Global Initiative for Asthma (GINA) no longer recommends SABA-only asthma treatment without an inhaled corticosteroid (ICS). Discharge asthma patients on an ICS-containing regimen. Never SABA alone.
  • Alternatives to SABA-only relief: GINA 2026 adds ICS-formoterol as an option to SABA for mild exacerbations (age 6 yr and older). It also lists as-needed budesonide-albuterol (Airsupra, adults) as an anti-inflammatory reliever. The US 2020 NAEPP updates endorse ICS-formoterol single-inhaler therapy and as-needed ICS with SABA.
Not for bronchiolitis: Don't give albuterol to infants and children 1–23 months old with bronchiolitis. The American Academy of Pediatrics (AAP) makes that a strong recommendation. It does not shorten illness or hospital stay.

Dosing & Administration

Available Forms

  • Nebulizer solution 0.083%: 2.5 mg/3 mL unit-dose vial. Ready to use, no dilution. Labeled for age 2 yr and older weighing ≥15 kg.
  • Nebulizer concentrate 0.5%: 5 mg/mL. The 2.5 mg/0.5 mL vial is diluted to 3 mL with sterile saline, and it is the one for continuous nebulization. The unit-dose vial is labeled for age 12 yr and older. Pediatric weight-based use (EPR-3 continuous dose) is off-label.
  • Low-strength nebulizer solution: 0.63 mg/3 mL (0.021%) and 1.25 mg/3 mL (0.042%). Labeled for relief of bronchospasm in children 2–12 yr (3–4 times daily). They were not studied in acute attacks (label), so use 2.5 mg for exacerbations.
  • Metered-dose inhaler (MDI), HFA: 90 mcg albuterol (108 mcg albuterol sulfate) per actuation; 60- or 200-actuation canisters with a dose counter.
  • Dry-powder inhaler (DPI): 90 mcg per inhalation (ProAir RespiClick, Digihaler). It is breath-actuated and contains lactose. Age 4 yr and older: 2 inhalations every 4–6 hr. For exercise-induced bronchospasm, take 2 inhalations 15–30 min before exercise. There is no priming. Don't use a spacer or holding chamber with it.
  • Oral: 2 mg and 4 mg tablets, and syrup 2 mg/5 mL. It's too slow for acute bronchospasm.
  • Combinations: ipratropium-albuterol nebulizer solution (DuoNeb): 0.5 mg ipratropium and 2.5 mg albuterol (as 3 mg albuterol sulfate) in 3 mL; Combivent Respimat (ipratropium-albuterol); Airsupra (albuterol-budesonide).

Adult Dosing

IndicationDose & RouteRepeat / MaxNotes
Asthma exacerbation: nebulizer (US EPR-3, 2007)
2.5–5 mg nebulized
Every 20 min for 3 doses, then 2.5–10 mg every 1–4 hr as needed
Add ipratropium 0.5 mg to the first 3 doses in moderate to severe attacks. Differs from FDA label: label is 2.5 mg three to four times daily (ages 2–12), and says more frequent or higher doses are not recommended.
Asthma exacerbation: MDI (US EPR-3, 2007)
4–8 puffs (90 mcg/puff) INH (MDI with spacer)
Every 20 min for up to 4 hr, then every 1–4 hr as needed
Equal to a nebulizer in mild to moderate attacks with coached technique. Differs from FDA label: label is 2 inhalations every 4–6 hr (ages 4 and older).
Asthma exacerbation: GINA 2026 (age 6 yr and older)
Mild: 4 puffs INH (MDI with spacer). Moderate: 4–6 puffs or 2.5 mg nebulized. Severe: 6–10 puffs or 5 mg nebulized
Mild: repeat once after 30–60 min if needed. Moderate or severe: up to 3 times, 20–30 min apart; review at 1 hr
Add ipratropium for moderate and severe attacks. More conservative than EPR-3 (fewer puffs in mild and moderate attacks, at most 3 repeats and then reassess) because SABA over-treatment causes toxicity (lactic acidosis). GINA puffs are 100 mcg metered (90 mcg delivered, the US label strength).
Severe asthma: continuous
10–15 mg/hr continuous nebulization (not weight-based)
Upper end 15 mg/hr; review response at 1 hr
Large-volume nebulizer; continuous ECG and K⁺ checks. Evidence vs intermittent dosing is mixed, per GINA 2026. Differs from FDA label: label says more frequent administration is not recommended.
COPD exacerbation
2.5 mg nebulized (standard unit dose; air-driven), or 1–2 puffs INH (MDI)
Every 1 hr for 2–3 doses, then every 2–4 hr by response; avoid high doses
GOLD 2026 sets the frequency, not the mg dose. Give oxygen separately by nasal cannula: oxygen-driven nebulization can raise PaCO₂.
Hyperkalemia (off-label adjunct, K⁺ ≥6.5 mEq/L; optional at 6.0–6.4)
10–20 mg nebulized
Single dose; 10 mg in ischemic heart disease
Add-on to calcium and IV insulin-glucose (UK Kidney Association: add-on, not monotherapy in severe hyperkalemia). Not used in hyperkalemic cardiac arrest (AHA 2025 Part 10, COR 3). Off-label dose (label nebulized dose is 2.5 mg for asthma). 10–20 mg is from UKKA 2026. 10 mg is four 2.5 mg vials. Lowers K⁺ about 0.5–1 mEq/L.
Bronchospasm with anaphylaxis
2.5–5 mg nebulized, or 4–8 puffs INH (MDI with spacer)
Repeat as for asthma
Adjunct for bronchospasm only, after IM epinephrine. GINA 2026: give epinephrine first, then bronchodilator. Albuterol does not treat airway edema or shock; see Indications.
Routine relief; exercise-induced bronchospasm
2 puffs INH (MDI) (1 puff may suffice); or 2.5 mg nebulized
Every 4–6 hr (nebulized: 3–4 times daily); exercise: 2 puffs 15–30 min before
Labeled regimen; needing more signals worsening control.

Pediatric Dosing

IndicationDose (per kg) & RouteMax Single / Max TotalNotes
Asthma exacerbation: mild wheeze without distress (age 2 yr and older; NASEMSO v3.0)
2.5 mg nebulized
Max 5 mg per dose (adult dose; NASEMSO p. 13)
Matches the label dose (2.5 mg three to four times daily, ages 2–12). Under 2 yr: not covered by this guideline (NASEMSO p. 190). Do not give in bronchiolitis (AAP).
Asthma exacerbation: respiratory distress with bronchospasm (age 2 yr and older; NASEMSO v3.0)
5 mg nebulized, or 6 puffs INH (MDI with spacer)
Repeat at that dose for ongoing distress; max 5 mg per dose
Differs from FDA label: label dose (ages 2–12, at least 15 kg) is 2.5 mg nebulized 3–4 times daily, and the label says higher doses or more frequent use are not recommended; the MDI label dose for age 4 and older is 2 puffs every 4–6 hr. The 5 mg or 6-puff distress dose and unlimited repeats are off-label (NASEMSO p. 191). EPR-3 0.15 mg/kg nebulized (min 2.5 mg, max 5 mg) every 20 min ×3, and 4–8 puffs; GINA 2026 is more conservative.
Severe asthma: continuous (ED, PICU or critical-care transport)
0.5 mg/kg/hr continuous nebulization (EPR-3; off-label)
No fixed max: titrate to effect
Continuous ECG and K⁺ checks. Weight-based use is off-label.
Bronchiolitis (1–23 months)
Not recommended
Not applicable
AAP: do not give albuterol in bronchiolitis (strong recommendation).
Hyperkalemia (specialist use)
Not established: per pediatric protocol. Studies in ages 5–18 used 2.5–5 mg nebulized (off-label; UKKA 2026)
Not established
Lowered K⁺ about 0.6 mEq/L, peak at 30 min, in one pediatric study (age 5–18 yr). Off-label.
Routine relief (labeled)
MDI: 2 puffs (age 4 yr and older). Nebulized: 2.5 mg (age 2 yr and older, ≥15 kg)
MDI every 4–6 hr; nebulized 3–4 times daily
Low-strength vials (0.63 or 1.25 mg) were not studied in acute attacks (label); use 2.5 mg for exacerbations.
Neonates
Not established in neonates
Specialist use only
Neonatal ICU decision.

Pediatric doses come from AHA/AAP 2025 when that source states a dose. Next comes the NASEMSO National Model EMS Clinical Guidelines v3.0 (2022), then the US label. If none of them gives a dose, this page shows none. A pediatric maximum never goes above the adult maximum dose (NASEMSO Universal Care Guideline, p. 13). Unless a dose is marked labeled, treat it as off-label. Check your weight math here: pediatric weight-based dosing.

Preparation & Administration

  • MDI check: Read the dose counter (discard at 000). Prime if new, unused for more than 2 weeks or dropped (Ventolin HFA: 4 sprays, shaking before each).
  • MDI with spacer: Shake before every puff and give one puff at a time into the spacer, with 5–6 breaths after each, per GINA 2026; follow the spacer's instructions for use.
  • Mask or mouthpiece: Face mask for children 0–3 yr; switch to a mouthpiece as soon as the child can use it, per GINA 2026. Some spacers need a detergent wash (without rinsing) or 2–4 priming puffs to reduce static, per GINA 2026.
  • Nebulizer: Use the whole 3 mL unit-dose vial (2.5 mg of 0.083%) (label). In COPD, drive it with air. GOLD 2026 notes oxygen-driven nebulization can raise PaCO₂. In children with low saturation, an oxygen-driven nebulizer may be used, per GINA 2026.
  • Continuous nebulization: Large-volume nebulizer; document the hourly dose.
  • Intubated or ventilated patient (MDI in-line): Place a spacer or chamber adapter in the inspiratory limb and leave it in the circuit. Shake the MDI, remove the heat and moisture exchanger (HME) during delivery and do not change ventilator settings. Actuate at the onset of inspiration and repeat every 20–30 s until the dose is given. Start with 4–6 puffs. Titrate to response: a falling peak-to-plateau pressure gap, less auto-PEEP, better expiratory flow. Repeat every 3–4 hr, sooner in status asthmaticus. Continuous in-line nebulizer flow can cause missed triggers and hypoventilation that ventilator alarms may not catch. Watch the delivered tidal volumes. Bag-ventilated patients: in-line adapter per agency protocol. Follow agency or respiratory therapy protocol.
Video 1: Metered-dose inhaler used with a spacer, step by step. Use it to coach patients and to check technique before calling an MDI dose a failure. Source: COPD Foundation (YouTube)

Contraindications & Precautions

Contraindications

  • Hypersensitivity to albuterol or any product component
  • DPI products (ProAir RespiClick, Digihaler): severe milk-protein hypersensitivity (lactose carrier)

Precautions

  • Cardiovascular disease: coronary insufficiency, arrhythmia, hypertension. Here's what β-agonists do to the tracing: they can flatten T waves, prolong QTc and depress ST segments.
  • Seizure disorder, hyperthyroidism, diabetes: The response is exaggerated. Large IV doses have worsened diabetes and ketoacidosis.
  • Rising use: needing more doses than usual means the asthma is getting worse. Reassess, and treat the inflammation. Excessive use of inhaled sympathomimetics has been fatal.
  • Labor: It may relax the uterus. It isn't approved for preterm labor, where pulmonary edema has been reported with β2-agonist tocolysis.
  • Hypokalemia risk: loop or thiazide diuretics, high or continuous doses, hypoxia.

Hold / Reassess If

  • Wheeze or dyspnea worsens right after a dose. Suspect paradoxical bronchospasm. Stop, and switch therapy
  • New chest pain, ischemic ST change or new tachyarrhythmia: stop dosing, 12-lead ECG
  • Lactate rising, or breathing faster while air entry improves? Consider β-agonist toxicity before giving more
  • Hyperkalemia with ischemic heart disease: limit the dose to 10 mg with cardiac monitoring
Silent chest: Absent wheeze in a tiring, drowsy or confused patient signals near-arrest. It does not mean they're getting better. Keep the bronchodilators running and get ventilatory support ready.

Adverse Effects & Toxicity

Common

  • Tremor: about 20% with nebulized doses
  • Throat irritation: about 10% with MDI; cough about 5%
  • Dizziness: about 7%; nervousness and nausea about 4%; headache about 3%
  • Tachycardia, palpitations: dose-related

Serious / Life-Threatening

EffectRecognitionManagement
Tachyarrhythmia
Atrial fibrillation, SVT, extrasystoles on the monitor
Stop dosing, 12-lead ECG, check K⁺; treat the rhythm per ACLS
Myocardial ischemia
Angina, ST depression
Stop; serial ECG and troponin
Hypokalemia
Falling K⁺, U waves, ectopy
Usually transient; replace if low with arrhythmia
Lactic acidosis, hyperglycemia
Rising lactate and glucose, tachypnea despite better airflow
Recognize as drug effect; reassess before stacking more albuterol
Paradoxical bronchospasm
Worse wheeze right after a dose, often with the first use of a new canister or vial
Stop; switch to an alternative bronchodilator
Hypersensitivity, anaphylaxis
Urticaria, angioedema, hypotension
Stop; IM epinephrine first, per GINA 2026, then bronchodilator

Overdose & Toxicity Management

  • Signs: tachycardia, arrhythmia, angina, hypertension or hypotension, tremor, seizures, hypokalemia, hyperglycemia, metabolic acidosis; cardiac arrest has occurred.
  • Immediate management: stop albuterol; continuous ECG; check K⁺, glucose and a blood gas with lactate; symptomatic care.
  • Antidote: none. Give supportive care and treat the complications. The label says a cardioselective β-blocker may be considered, keeping in mind that it can cause bronchospasm (HFA label, Overdosage).

Monitoring

ParameterWhen / How OftenTarget / Act If
Clinical: work of breathing, air entry, speech
Before and after each dose; formal review at 1 hr
Drowsy, confused or silent chest: escalate (magnesium, ventilatory support)
Clinical: peak flow (PEF) or FEV₁
Before treatment and at 1 hr when the patient can perform it
PEF >60–80% of predicted or personal best, sustained 3–4 hr: no further SABA needed in the ED. Consider discharge at PEF or FEV₁ >70% of personal best or predicted with mild features for 1–2 hr after the last dose, on an ICS-containing regimen with a reliever
Clinical: SpO₂
Continuous
Asthma, per GINA 2026: give oxygen only if SpO₂ is below 92%, and titrate to 92 to 95% (children 5 years and younger: at least 92%); in adults do not exceed 96%. COPD or other risk of hypercapnic failure: target 88 to 92% pending a blood gas
Clinical: HR and rhythm
Continuous ECG with continuous or high-dose therapy
New arrhythmia or ST change: stop, 12-lead ECG
Laboratory: potassium
Baseline and after repeated or continuous dosing
K⁺ low with ectopy: replace and recheck
Laboratory: lactate, glucose
Persistent tachypnea, diabetes, high doses
Rising lactate with better airflow suggests drug effect, not failure
Hyperkalemia treatment
K⁺ at 1, 2, 4, 6 and 24 hr
Rebound at 4–6 hr as albuterol and insulin wear off: arrange definitive K⁺ removal
Drug levels: digoxin
Patients on digoxin with prolonged high-dose albuterol
Single IV or oral albuterol doses lowered digoxin levels 16–22% in volunteers; relevance for inhaled use is unclear: consider a digoxin level

Interactions & Compatibility

Clinically Significant Interactions

Drug / ClassEffectWhat To Do
β-blockers (especially nonselective, e.g. propranolol)
Block bronchodilation; may cause severe bronchospasm
Avoid in asthma; a cardioselective agent only if essential, with caution
Other sympathomimetics (epinephrine, terbutaline)
Additive tachycardia and arrhythmia
Do not combine with another short-acting inhaled β-agonist (sympathomimetic) bronchodilator; ipratropium is fine. Other adrenergic drugs by any route with caution (continuous ECG, K⁺)
Loop and thiazide diuretics
Worse hypokalemia and ECG changes
Monitor K⁺ and ECG
MAOIs, tricyclic antidepressants (including within 2 weeks of stopping)
Potentiated vascular effects
Give with extreme caution
Digoxin
Single IV or oral albuterol doses lowered serum digoxin 16–22% in volunteers; relevance for inhaled use is unclear
Consider a digoxin level with prolonged high-dose therapy
Methylxanthines (aminophylline, theophylline)
Arrhythmias and sudden death in animal studies with β-agonists
Continuous ECG if combined

Nebulizer Compatibility

  • Inhaled drug, so IV compatibility doesn't apply.
  • It may be mixed with ipratropium nebulizer solution in the same cup.
  • Other nebulized drugs have no established compatibility. Give them separately.
  • Verify with an institutional compatibility resource.

Special Populations

  • Pediatrics: MDI labeled from 4 yr. Nebulizer solution 0.083% and low-strength vials from 2 yr. The 0.5% unit-dose vial from 12 yr (pediatric weight-based use is off-label). Guidelines still use a spacer and mask in younger children with acute asthma. Don't give it in bronchiolitis. The doses are in the Pediatric Dosing table.
  • Neonates: Not established. Neonatal hyperkalemia use belongs to the specialist.
  • Pregnancy: Human data have not consistently shown a risk of birth defects or miscarriage with inhaled albuterol. Cleft palate showed up in mice. Poorly controlled asthma raises the risk of preeclampsia, prematurity and low birth weight. So treat exacerbations fully.
  • Lactation: There are no human milk data. Plasma levels after inhaled doses are low, so milk levels are likely low too. Don't withhold treatment.
  • Older Adults: Start at the low end. Cardiac disease and interacting drugs are common in this group.
  • Renal Impairment: The label gives no adjustment for inhaled albuterol. The absorbed drug and its metabolite leave the body mainly in urine. Racemic albuterol clearance fell 67% in renal impairment (CrCl 7–53 mL/min). Use caution with high doses, such as 10–20 mg for hyperkalemia, and monitor HR, rhythm and K⁺. Up to 40% of patients with end-stage renal disease (ESRD) do not lower K⁺ with albuterol.
  • Hepatic Impairment: No specific adjustment established.
  • Obesity / Dosing Weight: Adult doses are fixed. A pediatric dose never goes above the adult maximum. The only weight-based pediatric dose on this page is the continuous 0.5 mg/kg/hr (EPR-3).
  • Hypercapnic COPD: Drive nebulizers with air, and give titrated oxygen separately. In COPD or any other risk of hypercapnic failure, target 88 to 92% until you have a blood gas.

Field & Transport Considerations

  • Scope: EMT through critical-care transport give or assist with albuterol. It varies by state and agency protocol.
  • Storage & Stability: Keep the MDI at 20–25°C (68–77°F). Excursions to 15–30°C (59–86°F) are allowed. Canisters can burst above 49°C (120°F), so don't leave them on a hot dash. Nebulizer vials go at 2–25°C (36–77°F) in the foil pouch, protected from light.
  • Carried Concentration: 0.083% (2.5 mg in 3 mL, ready to use) and 0.5% (2.5 mg in 0.5 mL, dilute first) give the same dose in very different volumes. Read the label before you draw up continuous or off-label doses.
  • Device Choice: An MDI with spacer works as well as a nebulizer when technique is coached (EPR-3). GINA 2026 prefers the spacer if the patient can use it. If they can't, use a nebulizer. Nebulizers can transmit respiratory viral particles at least 1 m, per GINA 2026. Where infection risk matters, prefer the spacer.
  • Altitude / Environment: Set the oxygen saturation target for altitude, per GINA 2026.
  • Continuous Nebulization in Transport: Confirm the hourly dose, remaining volume for the trip, ECG monitoring and last K⁺.
  • Ventilated Patients: Give MDI puffs through an in-line spacer in the inspiratory limb (Preparation & Administration). If a continuous in-line nebulizer is running, watch the delivered volumes.
  • Handoff Essentials: total albuterol given (mg or puffs) and times, ipratropium, magnesium, steroid and epinephrine doses, response (work of breathing, SpO₂, PEF), HR trend.

Clinical Pearls

Anaphylaxis first: Anaphylaxis and asthma together? Give IM epinephrine first. Then start the bronchodilator, per GINA 2026. Albuterol is the adjunct for bronchospasm only. It does not treat airway edema or shock. AHA 2025 Part 10 lists epinephrine and bronchodilators among the peri-arrest anaphylaxis options.
Toxicity mimics failure: Big doses cause tachycardia, hypokalemia, lactic acidosis and hyperventilation. Read that as worsening asthma, and you'll stack even more albuterol on top.
Spacer equals nebulizer in mild to moderate attacks: An MDI with spacer works as well as a nebulizer when technique is coached (EPR-3). Don't call the MDI a failure until you've coached the technique. In children, GINA 2026 also found fewer adverse effects and a shorter ED stay with a spacer than with a nebulizer.
Levalbuterol vs albuterol:
  • Levalbuterol is the active R-enantiomer of racemic albuterol.
  • Half the milligrams gives comparable efficacy and safety: 0.63 mg levalbuterol ≈ 1.25 mg albuterol.
  • It has not been evaluated for continuous nebulization. The nebulized form is labeled from 6 yr.
  • The MDI is 45 mcg per puff, dosed like the albuterol MDI.
Exam discriminator: shift, not removal: Albuterol and insulin push K⁺ into the cells. Total body K⁺ doesn't change, and levels rebound at 4–6 hr. Real removal takes a potassium binder or dialysis.
COPD: air, not oxygen, through the nebulizer: Oxygen-driven nebulization can raise PaCO₂ in a COPD exacerbation. Put the nebulizer on air. Titrate oxygen by nasal cannula to SpO₂ 88–92%.

Pharmacology

Mechanism of Action

  • β2-receptor agonist → adenylyl cyclase → more cyclic AMP → airway smooth-muscle relaxation from trachea to terminal bronchioles. The trigger doesn't matter.
  • Cyclic AMP also inhibits mediator release from airway mast cells.
  • Na⁺/K⁺-ATPase stimulation → K⁺ shifts into cells (therapeutic in hyperkalemia, adverse in asthma).
  • β2 receptors make up 10–50% of cardiac β-receptors. Even a selective agonist causes tachycardia.

Pharmacokinetics

RouteOnsetPeakDuration
INH (MDI)
~5 min
~1 hr
3–6 hr (about 4 hr typical)
INH (MDI), children 4–11 yr
~8 min
~1.5 hr
More than 3 hr (up to 6 hr in some)
INH (nebulized)
~5 min
~1 hr, near peak for 2 hr
3–6 hr (3–4 hr in most)
INH (K⁺ lowering, 10–20 mg)
Within 30 min
30–120 min
At least 2 hr
PO
Within 30 min
2–3 hr
4–6 hr; may last 6–8 hr or longer (label)
  • Half-life: about 4.6 hr after inhalation; 5–6 hr after oral dosing.
  • Absorption: Less than 20% of a nebulized dose is absorbed. The rest stays in the device or gets exhaled.
  • Protein binding: low (about 10%).
  • Metabolism: sulfation, mainly by the sulfotransferase SULT1A3. Swallowed drug is largely metabolized in the gut. After an oral dose, about 60% of the drug recovered in urine is metabolite.
  • Elimination: renal, 80–100% as parent drug or its primary metabolite, most within 24 hr; less than 20% in feces.
  • Stereochemistry: It is racemic. The R-enantiomer (levalbuterol) carries the bronchodilator activity.

Names & Classification

Generic Name
Albuterol sulfate (international name: salbutamol)
Brand Names
Ventolin HFA; ProAir RespiClick and ProAir Digihaler (DPI); Proventil HFA and ProAir HFA (older MDI brands); combinations: Combivent Respimat (ipratropium-albuterol), Airsupra (albuterol-budesonide, as-needed reliever for adults)
Pharmacologic Class
Short-acting β2-adrenergic agonist (SABA)
Therapeutic Class
Bronchodilator; potassium-shifting adjunct (off-label)
Controlled Substance
Not controlled
ISMP High-Alert
No
Look-Alike / Sound-Alike
None on the ISMP confused-names list; the risk is concentration: 0.083% (2.5 mg/3 mL) vs 0.5% (2.5 mg/0.5 mL)

References

  1. GlaxoSmithKline. (2026). Ventolin HFA (albuterol sulfate) inhalation aerosol [prescribing information]. DailyMed, National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d92c5d6b-ff10-4087-36a2-1cfc464cb967. Other labels used (current DailyMed versions): albuterol inhalation solution 0.083%, https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b72742df-1a6b-4483-aff3-3e79db5e015d; 0.5%, https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fdb4ac5a-bf0d-4896-89f7-1828c081b79e; 0.63 mg and 1.25 mg per 3 mL, https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d4c532be-1f41-60d3-e053-2995a90a98be (Ritedose); ProAir RespiClick (Teva), https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9324e2eb-26fd-4f14-9f10-e5aa467306f4; albuterol tablets (Zydus), https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c3fa0068-fd12-45de-818e-e929fb45ba05; levalbuterol inhalation solution (Ritedose), https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d6998949-e1cb-4c86-a480-c0dfd9cb75b5.
  2. Global Initiative for Asthma. (2026). Global strategy for asthma management and prevention, 2026 update. https://ginasthma.org/2026-gina-strategy-report/
  3. Global Initiative for Chronic Obstructive Lung Disease. (2026). Global strategy for prevention, diagnosis and management of COPD: 2026 report. https://goldcopd.org/2026-gold-report/.
  4. O'Driscoll, B. R., Howard, L. S., Earis, J., Mak, V., et al. (2017). British Thoracic Society guideline for oxygen use in adults in healthcare and emergency settings. BMJ Open Respiratory Research, 4(1), e000170. https://doi.org/10.1136/bmjresp-2016-000170.
  5. National Asthma Education and Prevention Program. (2007). Expert Panel Report 3: Guidelines for the diagnosis and management of asthma (landmark guideline; its exacerbation doses remain current US guidance). National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/sites/default/files/media/docs/EPR-3_Asthma_Full_Report_2007.pdf.
  6. Cloutier, M. M., Baptist, A. P., Blake, K. V., et al. (2020). 2020 focused updates to the asthma management guidelines. Journal of Allergy and Clinical Immunology, 146(6), 1217–1270. https://doi.org/10.1016/j.jaci.2020.10.003.
  7. Georgopoulos, D., Mouloudi, E., Kondili, E., & Klimathianaki, M. (2000). Bronchodilator delivery with metered-dose inhaler during mechanical ventilation. Critical Care, 4(4), 227–234. https://doi.org/10.1186/cc698.
  8. Ralston, S. L., Lieberthal, A. S., Meissner, H. C., et al. (2014). Clinical practice guideline: the diagnosis, management, and prevention of bronchiolitis (current AAP guideline). Pediatrics, 134(5), e1474–e1502. https://doi.org/10.1542/peds.2014-2742
  9. Alfonzo, A., Harrison, A., Baines, R., Chu, A., Mann, S., & MacRury, M. (2026). Clinical practice guidelines: treatment of acute hyperkalaemia in adults (updated July 2026). UK Kidney Association. https://www.ukkidney.org/sites/default/files/documents/FINAL%20VERSION%20-%20UKKA%20CLINICAL%20PRACTICE%20GUIDELINE%20-%20MANAGEMENT%20OF%20HYPERKALAEMIA%20IN%20ADULTS%20-%20UPDATED%20JULY%202026_0.pdf
  10. Jessen, M. K., Andersen, L. W., Djakow, J., et al. (2025). Pharmacological interventions for the acute treatment of hyperkalaemia: a systematic review and meta-analysis. Resuscitation, 208, 110489. https://doi.org/10.1016/j.resuscitation.2025.110489.
  11. American Heart Association. (2025). 2025 American Heart Association Guidelines for CPR and ECC, Part 10: Adult and Pediatric Special Circumstances of Resuscitation. https://cpr.heart.org/en/resuscitation-science/cpr-and-ecc-guidelines/adult-and-pediatric-special-circumstances-of-resuscitation.
  12. National Association of State EMS Officials. (2022). National Model EMS Clinical Guidelines, Version 3.0. https://nasemso.org/content.aspx?page_id=22&club_id=157064&module_id=701974.

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