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Propafenone

  • AntiarrhythmicsAntiarrhythmics

A class IC antiarrhythmic with mild beta-blocking action, used to keep sinus rhythm in atrial fibrillation in hearts without structural disease.

Updated

Quick facts

Group
Antiarrhythmics
Target
Cardiac sodium channel Nav1.5 (and β-adrenergic receptors)
Used for
Prolonging the time to recurrence
Key effects
Unusual or metallic taste · Nausea · Dizziness
Monitor
ECG before and during treatment
ATC
C01BC03

No doses: the clinician sets them by the current guideline.

Mechanism of action

The figure shows propafenone bound to the rat cardiac sodium channel Nav1.5, very similar to the human channel.

Target in 3D: Cardiac sodium channel Nav1.5 (and β-adrenergic receptors). PDB structure 7FBS (RCSB PDB, public domain). View the structure at RCSB PDB

Propafenone blocks the fast inward sodium current, mainly in Purkinje fibres, slowing the action potential upstroke and conduction (longer PR and QRS). It also has weak beta-blocking activity, which can slow the heart and narrow the airways, and a local anaesthetic effect.

  1. Propafenone blocks the Nav1.5 sodium channel
  2. Conduction slows: longer PR and wider QRS
  3. Weak beta blockade adds slowing of the heart

Indications

Adverse effects

Common

  • Unusual or metallic taste
  • Nausea, vomiting and constipation
  • Dizziness, headache and fatigue
  • First-degree AV block and QRS widening

Contraindications

  • Heart failure or cardiogenic shock
  • Sinoatrial, AV or intraventricular conduction disorders without a pacemaker
  • Known Brugada syndrome
  • Bradycardia or marked hypotension
  • Bronchospastic disorders and severe obstructive lung disease
  • Marked electrolyte imbalance

Key interactions

CYP2D6 inhibitors combined with CYP3A4 inhibitors
Large rise in propafenone levels and proarrhythmia; the combination is avoided
Digoxin
Higher digoxin levels
Warfarin
Higher warfarin levels; INR is checked
Lidocaine
More central nervous system effects

What is monitored

  • ECG before and during treatment: PR and QRS
  • Blood count if infection signs appear
  • Pacemaker function in patients with devices

Administration and safety

  • Used only in hearts without structural disease; ECG is taken before starting.
  • In atrial fibrillation or flutter it is given with a drug that slows the AV node.
  • Immediate-release and extended-release products are not interchangeable one for one: the product is checked.

Pregnancy and breastfeeding

Human data are limited; it is used in pregnancy only if the benefit justifies the risk to the fetus.

Nursing care

  • Check pulse and ECG; report QRS widening, fainting or palpitations.
  • Ask about wheeze or breathlessness in patients with lung disease.
  • Teach the patient to report fever, sore throat or chills (agranulocytosis).

Pharmacokinetics

Metabolism
Liver, mainly CYP2D6 (also CYP3A4 and CYP1A2); poor CYP2D6 metabolisers reach higher levels
Elimination
Mostly as metabolites; dose is lowered in liver impairment

Test yourself

Think of the answer, then tap the question to see it.

What property distinguishes propafenone from flecainide?

Weak beta-blocking activity, so it can cause bradycardia and bronchospasm.

Which inherited ECG syndrome can propafenone unmask?

Brugada syndrome.

Why do some patients reach much higher propafenone levels?

They are poor CYP2D6 metabolisers or take CYP2D6 and CYP3A4 inhibitors together.

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Connections

← Back to the class: Antiarrhythmics

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: DailyMed - PROPAFENONE HYDROCHLORIDE tablet, film coated (DailyMed (U.S. National Library of Medicine), 2026); Propafenone: MedlinePlus Drug Information (MedlinePlus (U.S. National Library of Medicine), 2026); ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026); 7FBS: structure of a channel (RCSB Protein Data Bank, 2021).

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Representative model, for educational purposes only.