BOXED WARNING Prolonged use often produces positive ANA and a lupus erythematosus-like syndrome; risk of blood dyscrasias (agranulocytosis, bone marrow depression); reserve for life-threatening ventricular arrhythmias.
FDA dosing
Population
Start
Target
Max
Ventricular arrhythmias (IM)
Adult
50 mg/kg/day in divided doses q3-6h
per response/levels
per response
Ventricular arrhythmias (IV)
Adult
IV load slowly, rate not to exceed 50 mg/min, under ECG monitoring
per response
per response
Arrhythmias with anesthesia/surgery (IM)
Adult
100-500 mg IM
Renal Reduce dose/frequency in renal impairment (adjust for age and renal function)
Hepatic Undefined
IV administration rate not to exceed 50 mg/min
Instructions
IV: dilute and give slowly, not exceeding 50 mg/min, with ECG and blood pressure monitoring
Switch to oral procainamide for long-term maintenance
Contraindications
Complete heart block
Second-degree AV block or hemiblock (unless ventricular rate controlled by pacemaker)
Established systemic lupus erythematosus
Torsades de pointes (Group 1A antiarrhythmics contraindicated)