Corvert

— THERAPEUTIC CATEGORIES —
  • CHF and arrhythmias

Corvert Generic Name & Formulations

General Description

Ibutilide fumarate 0.1mg/mL; soln for IV infusion.

Pharmacological Class

Class III antiarrhythmic.

How Supplied

Single-dose vial (10mL)—1

Manufacturer

Corvert Indications

Indications

Rapid conversion of atrial fibrillation or atrial flutter of recent onset to sinus rhythm.

Corvert Dosage and Administration

Adult

Give by IV infusion over 10 minutes. ≥18yrs: (≥60kg) initially 1mg; (<60kg) initially 0.01mg/kg. If no response, may repeat second 10-minute infusion of equal strength given 10 minutes after first infusion. Discontinue infusion as soon as the presenting arrhythmia has terminated, or if sustained/nonsustained ventricular tachycardia or marked QT prolongation occurs.

Children

<18yrs: not recommended.

Corvert Contraindications

Not Applicable

Corvert Boxed Warnings

Not Applicable

Corvert Warnings/Precautions

Warnings/Precautions

Risk of fatal arrhythmias (eg, sustained polymorphic ventricular tachycardia, usually associated with QT prolongation (torsades de pointes), but sometimes without documented QT prolongation may occur. Be experienced with the treatment and monitoring of life-threatening arrhythmias before administering. Have cardiac monitoring equipment and proper medication available. Correct hypokalemia and hypomagnesemia before starting. Monitor ECG continuously for at least 4 hours post infusion or until QTC returned to baseline. Proarrhythmia conditions (eg, ventricular arrhythmias, atrial flutter or fibrillation, QTC intervals >440 msec, hypokalemia, history of CHF, low left ventricular ejection fraction). Previous polymorphic ventricular tachycardia: not recommended. Renal or hepatic dysfunction (monitor). Pregnancy (Cat.C). Nursing mothers: not recommended.

Corvert Pharmacokinetics

See Literature

Corvert Interactions

Interactions

Class Ia antiarrhythmics (eg, disopyramide, quinidine, procainamide) or other Class III drugs (eg, amiodarone, sotalol): do not give concomitantly or within 4 hours post-infusion. QT prolongation with phenothiazines, tricyclic and tetracyclic antidepressants, H1 receptor antagonists. Caution with digoxin.

Corvert Adverse Reactions

Adverse Reactions

Ventricular extrasystoles, sustained or nonsustained polymorphic ventricular tachycardia, sustained monomorphic ventricular tachycardia, headache, hypo- or hypertension, tachycardia, bundle branch block, AV block, nausea, QT segment prolonged, bradycardia.

Corvert Clinical Trials

See Literature

Corvert Note

Not Applicable

Corvert Patient Counseling

See Literature