Mechanism of action: Sotalol balliculeVisual mnemonic: Sotalol mascot “Better pace (yourself), Soda, LOL” LOL hat → beta blocker QT prolongation
What it isBeta-1 antagonist with hERG blockade; atrial fibrillation and ventricular arrhythmias.
Why this oneUnlike ordinary beta blockers, hERG blockade adds rhythm maintenance — and substantial torsades risk.
What limits itInitiate with continuous ECG monitoring; renal clearance requires dose adjustment, and abrupt withdrawal is unsafe.
Molecular structure: Sotalol
Sotalol prescription history
Animated chart of estimated U.S. prescriptions per year, Antiarrhythmics (class I/III) (1930–2026). Sotalol enters in 1993 (estimated).
FDA-approved for
ventricular arrhythmias (1992)
atrial fibrillation (2000)
Sulfonamide
Sulfonamide-derived drug — label silent
A sulfonamide by structure, without the N4 aromatic amine or N1 heterocycle; the label carries no sulfonamide warning, and Khan lists it among drugs with no or weak evidence of cross-reactivity.
BOXED WARNING Life-threatening proarrhythmia (Torsade de Pointes with QT prolongation); initiate/reinitiate in a facility with cardiac resuscitation and continuous ECG monitoring; reduce dose, lengthen interval, or discontinue if QT ≥500 msec; adjust dosing interval by creatinine clearance
FDA dosing
Population
Start
Target
Max
Ventricular arrhythmias
Adults
80 mg BID
160–320 mg/day (2–3 divided doses)
320 mg/day (up to 480–640 mg/day in refractory cases)
Recurrence of AFIB/AFL
Adults
80 mg BID
120 mg BID
—
Ventricular arrhythmias or AFIB/AFL
Pediatric ≥~2 y (normal renal function)
1.2 mg/kg TID
Titrate by response, HR, QTc; ≥36 h between increments, preferably in-hospital
2.4 mg/kg TID
Ventricular arrhythmias or AFIB/AFL
Pediatric ≤~2 y
1.2 mg/kg TID × age factor (1 month: ×0.7 = 0.8 mg/kg TID; ~1 week: ×0.3 = 0.4 mg/kg)
Titrate using the same age-factor calculation
Undefined (age-factor reduction applies to titration)
Titration Increase in increments of 80 mg/day every 3 days (provided QTc <500 msec)
Renal Adjust the dosing interval based on creatinine clearance
Hepatic Undefined
Monitor QTc 2–4 hours after each dose uptitration; reduce dose or discontinue if QT ≥500 msec
Instructions
Withdraw other antiarrhythmic therapy before starting
Hospitalize for at least 3 days (or until steady state) on initiation/reinitiation with continuous ECG monitoring
Correct hypokalemia and hypomagnesemia before initiating
Do not abruptly discontinue (risk of coronary artery disease exacerbation)
If a dose is missed, take the next dose at the usual time; do not double
Available strengths
tab 80, 120, 160, 240 mg
sol 5 mg/mL
inj 15 mg/mL
Contraindications
Sinus bradycardia, sick sinus syndrome, or 2nd/3rd degree AV block (unless a functioning pacemaker is present)
Congenital or acquired long QT syndrome
Cardiogenic shock or decompensated heart failure
Serum potassium <4 mEq/L
Bronchial asthma or related bronchospastic conditions
Baseline QT interval >450 msec (for AFIB/AFL)
Cautions
QT prolongation and proarrhythmia (Torsade de Pointes)
Bradycardia / heart block / sick sinus syndrome
Hypotension
New-onset or worsening heart failure
Do not abruptly discontinue (coronary artery disease exacerbation)
May mask hypoglycemia symptoms or worsen hyperglycemia
Correct electrolyte disturbances
Adverse reactions
Fatigue
Bradycardia (<50 bpm)
Dyspnea
Proarrhythmia
Asthenia
Dizziness
Pregnancy Crosses placenta; fetal risks incl. growth restriction, bradycardia, hypoglycemia, possible intrauterine death; monitor neonate for beta-blockade
Lactation Present in human milk at high levels; do not breastfeed during treatment