propafenone

Brand: Rythmol

⚠ BBW Prototype: flecainide
Drug Class: antiarrhythmic (Class IC)
Drug Family: antiarrhythmic
Subclass: sodium channel blocker + weak beta-blocker
Organ Systems: cardiovascular

Mechanism of Action

Sodium channel blocker with additional weak beta-blocking and calcium channel blocking properties; slows conduction velocity.

fast sodium channelsbeta-1 adrenergic receptor (weak)

Indications

  • paroxysmal AF/SVT in structurally normal hearts
  • ventricular arrhythmias

Contraindications

  • structural heart disease
  • cardiogenic shock
  • severe bronchospasm (weak beta-block)
  • uncontrolled HF

Adverse Effects

Common

  • dizziness
  • metallic taste
  • nausea
  • bradycardia

Serious

  • proarrhythmia
  • worsening HF
  • 1:1 flutter

Pharmacokinetics (ADME)

Absorption 5-50% oral (extensive first-pass; CYP2D6 polymorphism dependent)
Distribution moderate
Metabolism extensive hepatic CYP2D6, CYP3A4
Excretion renal (<1% unchanged)
Half-life 2-10 hours
Onset 2-3 hours
Peak 3.5 hours
Duration 8-12 hours
Protein Binding 97%
Vd 3.6 L/kg

Drug Interactions

Drug / Agent Mechanism Severity
CYP2D6 inhibitors dramatically increased propafenone levels in extensive metabolizers major
warfarin increases warfarin levels — monitor INR major
digoxin increases digoxin concentrations moderate

Nursing Considerations

  1. Pill-in-pocket approach same as flecainide
  2. Metallic taste is common adverse effect
  3. Weak beta-blockade — may cause bronchospasm
  4. CYP2D6 poor metabolizers have 5-10x higher exposure

Clinical Pearls

  • Unique metallic taste adverse effect due to local anesthetic properties
  • Propafenone pill-in-pocket for AF cardioversion

Safety Profile

Pregnancy avoid
Lactation avoid
Renal Adjustment Required
Hepatic Adjustment Required
TDM Not required

Concordance Terms

Cross-referenced clinical concepts — click any term to see all content where it appears.