What happens if a patient takes an extra dose of flecainide (antiarrhythmic medication)?

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Management of Flecainide Overdose

An extra dose of flecainide can lead to life-threatening cardiac toxicity requiring immediate medical attention, especially in patients with underlying cardiac conditions. 1

Clinical Manifestations of Flecainide Overdose

Flecainide overdose can present with a spectrum of cardiac abnormalities:

  • Electrocardiographic changes:

    • QRS complex widening (>25% from baseline)
    • PR interval prolongation (>0.3 seconds)
    • QT interval prolongation
    • Development of new bundle branch block
  • Cardiac rhythm disturbances:

    • Ventricular tachyarrhythmias
    • Bradycardia
    • Atrial flutter with 1:1 AV conduction
    • AV nodal block
    • Asystole
    • Bundle branch block
  • Other symptoms:

    • Hypotension
    • Syncope
    • Convulsions
    • Nausea and vomiting
    • Dizziness
    • Visual disturbances
    • Cardiac arrest in severe cases

Management Algorithm

1. Immediate Assessment and Stabilization

  • Assess vital signs and cardiac monitoring
  • Obtain 12-lead ECG to evaluate QRS duration, PR interval, and rhythm
  • Establish IV access
  • Obtain baseline laboratory studies including electrolytes and renal function
  • Determine amount of extra dose taken and timing

2. Treatment Based on Severity

For Mild Overdose (minimal ECG changes, stable hemodynamics):

  • Close monitoring for at least 24 hours due to long half-life (12-27 hours) 1
  • Consider holding next scheduled dose
  • Monitor for development of symptoms or ECG changes

For Moderate to Severe Overdose:

First-line treatment:

  • Sodium bicarbonate therapy: Initial bolus of 1-2 mEq/kg IV (or 50-100 mL of 8.4% solution) followed by continuous infusion 2, 3
    • Goal: Narrow QRS complex and improve conduction
    • Monitor serum pH and electrolytes

Additional interventions as needed:

  • Calcium gluconate (1-2 g IV) to stabilize myocardial cell membranes 2, 4
  • Inotropic agents or cardiac stimulants (dopamine, dobutamine, isoproterenol) for hemodynamic support 1
  • Mechanically assisted ventilation if respiratory compromise occurs 1
  • Circulatory assist devices such as intra-aortic balloon pumping in severe cases 1
  • Transvenous pacing for significant conduction block 1
  • For refractory cases: Consider intravenous lipid emulsion therapy or extracorporeal membrane oxygenation (ECMO) 5

3. Important Considerations

  • Duration of treatment: Extended supportive care may be necessary due to flecainide's long half-life 1
  • Hemodialysis: Not effective for removing flecainide from the body 1
  • Urine acidification: Theoretically may promote drug excretion in cases with alkaline urine, but limited evidence supports this approach 1
  • Risk factors for increased toxicity:
    • Renal impairment (CrCl ≤35 mL/min)
    • Hepatic dysfunction
    • Heart failure
    • Concomitant amiodarone therapy
    • Electrolyte disturbances
    • Female gender 2

Prevention of Future Overdose

  • Patient education regarding proper dosing schedule and importance of medication adherence
  • Consider dose reduction in high-risk patients (renal impairment, elderly)
  • For patients using "pill-in-pocket" approach, reinforce clear instructions about maximum dosing and frequency 4
  • Regular ECG monitoring and plasma level checks in patients on chronic therapy

Caution

Death has been reported following ingestion of as little as 1000 mg of flecainide 1. Even a single extra dose can cause significant toxicity in patients with risk factors. Flecainide is contraindicated in patients with structural heart disease, coronary artery disease, or significant conduction abnormalities 6, 2.

References

Guideline

Flecainide Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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