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Beta-Blocker / IV Antiarrhythmic

Esmolol Hydrochloride Double Strength in plastic container

Osmolarity: ≈ 312 mOsm/LTonicity: IsotonicpH: 5.0 (4.5 - 5.5)

Clinical Indications

Rapid control of ventricular rate in patients with atrial fibrillation or atrial flutter in perioperative, postoperative, or emergent circumstances. Treatment of tachycardia and hypertension.

Dosing & Administration Rate

Loading dose (optional): 500 mcg/kg/min for 1 minute. Maintenance: 50-300 mcg/kg/min. Double strength (20 mg/mL) allows lower volume infusion in fluid-restricted patients.

Warnings & Precautions

Ultra-short acting beta-blocker (half-life 9 min). Risk of severe hypotension and bradycardia. Contraindicated in severe bradycardia, uncompensated heart failure, and cardiogenic shock.

Contraindications

Severe bradycardia. Uncompensated heart failure. Cardiogenic shock. Second- or third-degree AV block.

Pharmacology & Safety Profile

Mechanism of Action

Cardioselective beta-1-adrenergic receptor blocker with a very short duration of action. Decreases heart rate and cardiac output.

Adverse Reactions

Hypotension (common and sometimes severe), diaphoresis, dizziness, somnolence, confusion, bronchospasm (at high doses).

Compatibility Notes

Incompatible with sodium bicarbonate.

Electrolyte & Composition Profile

ComponentAmount / Concentration
Esmolol Hydrochloride20 mg/mL (Double Strength)
Sodium Chloride5.9 mg/mL
Sodium Acetate / Glacial Acetic AcidBuffer
Water for Injectionq.s.
Caloric Density0 kcal/L

Clinical Parameters

RouteIntravenous (infusion)
Fluid CategoryCrystalloid Solution
Required MonitoringVital signs, fluid intake/output, baseline electrolytes
Administration SetupPeripheral or central venous access. Must use calibrated infusion pump.
Pregnancy SafetyCategory C (FDA). Can cause fetal bradycardia and hypoglycemia. Used only when clearly needed.
StorageStore at 25°C. Protect from freezing and excessive heat.
Prescription Status Rx Only

Clinical Disclaimer: Data compiled from FDA DailyMed, Baxter/Fresenius prescribing information, and USP monographs. Always verify against the physical product label, your institution's IV protocols, and current pharmacist guidance before administration.

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