NATIONAL
CALIFORNIA
VENTURA
category
mechanism
Slows conduction time through the AV node, interrupting the re-entry pathways through the AV node, restoring normal sinus rhythm
indications

Paroxysmal supraventricular tachycardia: Treatment of paroxysmal supraventricular tachycardia; when clinically advisable, appropriate vagal maneuvers should be attempted prior to adenosine administration.

Note: Not effective for conversion of atrial fibrillation, atrial flutter, or ventricular tachycardia.

contraindications
  • hypersensitivity to adenosine or any component of the formulation
  • second- or third-degree AV block, sick sinus syndrome, or symptomatic bradycardia (except in patients with a functioning artificial pacemaker)
  • known or suspected bronchoconstrictive or bronchospastic lung disease, asthma.
dosing

Adult

Note: Recommended for hemodynamically stable patients who do not respond to vagal maneuvers or for hemodynamically unstable patients. Preparations should be made for synchronized direct-current cardioversion in case adenosine is ineffective.

IV: Initial: 6 mg over 1 to 2 seconds via a peripheral line, followed immediately by a 20 mL NS flush (Note: Initial dose should be reduced to 3 mg if administered via a central line or when administered by any route to patients with a heart transplant); if initial dose is not effective within 1 to 2 minutes, administer 12 mg using the same procedures; may repeat a second 12 mg dose if needed

Pediatric

Hemodynamically unstable:

Infants, Children, and Adolescents: Rapid IV, Intraosseous: Initial: 0.1 mg/kg (maximum initial dose: 6 mg/dose); if not effective, increase to 0.2 mg/kg (maximum dose: 12 mg/dose); follow each bolus with NS flush.

Hemodynamically stable:

Infants, Children, and Adolescents <50 kg: Rapid IV: : Initial dose: 0.05 to 0.1 mg/kg via peripheral or central line; maximum initial dose: 6 mg/dose; if not effective within 1 to 2 minutes, increase dose by 0.05 to 0.1 mg/kg increments every 1 to 2 minutes to a maximum single dose of 0.3 mg/kg or 12 mg (whichever is less) or until termination of paroxysmal supraventricular tachycardia (PSVT); follow each bolus with NS flush.

Children and Adolescents ≥50 kg: Rapid IV: Initial: 6 mg via peripheral line, if not effective within 1 to 2 minutes, 12 mg may be given; may repeat 12 mg bolus if needed; follow each bolus with NS flush.

administration

IV: For rapid IV bolus use; administer IV push over 1 to 2 seconds at a peripheral IV site as proximal as possible to trunk (not in lower arm, hand, lower leg, or foot); immediately after each bolus, administer a rapid NS flush (20 mL). Use of 2 syringes (one with adenosine dose and the other with NS flush) connected to a T-connector or stopcock is recommended. Alternatively, if no stopcock is available or the patient only has a single-port IV, prepare a single syringe with adenosine 6 mg and 18 mL of NS and administer at a peripheral IV site.

onset
Rapid
peak
IV
duration
Very brief
dosage form

Solution, Intravenous: 6 mg/2 mL (2 mL) vial

pregnancy class
C
adverse reactions
  • Cardiovascular:
    • Cardiac arrhythmia (transient and new arrhythmia after cardioversion; eg, atrial premature contractions, atrial fibrillation, premature ventricular contractions; 55%)
    • Chest pressure (and discomfort; 7% to 40%)
    • Atrioventricular block (infusion 6%; third-degree <1%)
    • Depression of ST segment on ECG (3%)
    • Hypotension (<1% to 2%)
  • Central nervous system:
    • Headache (2% to 18%)
    • Dizziness (≤12%)
    • Nervousness (2%)
    • Paresthesia (≤2%)
    • Numbness (1%)
  • Dermatologic:
    • Facial flushing (18% to 44%)
    • Diaphoresis (<1%)
  • Gastrointestinal:
    • Gastrointestinal distress (13%)
    • Nausea (3%)
  • Neuromuscular & skeletal:
    • Neck discomfort (includes throat, jaw; <1% to 15%)
    • Upper extremity discomfort (≤4%)
  • Respiratory:
    • Dyspnea (12% to 28%)
    • Hyperventilation (<1%)
structure
Responsive image
warnings