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Flecainide Injectable Solution
Flecainide is a Class IC antiarrhythmic agent that blocks cardiac sodium channels to slow conduction velocity and suppress abnormal electrical activity in the heart.
Flecainide is a Class IC antiarrhythmic agent that blocks cardiac sodium channels to slow conduction velocity and suppress abnormal electrical activity in the heart. Used for Paroxysmal supraventricular tachycardia (PSVT), Paroxysmal atrial fibrillation, Ventricular arrhythmias.
At a glance
| Generic name | Flecainide Injectable Solution |
|---|---|
| Sponsor | Hippocration General Hospital |
| Drug class | Class IC antiarrhythmic agent |
| Target | Cardiac voltage-gated sodium channel (Nav1.5) |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | Phase 3 |
Mechanism of action
Flecainide works by inhibiting fast inward sodium currents in cardiac tissue, which decreases the rate of depolarization and slows conduction through the atria and ventricles. This action suppresses ectopic activity and stabilizes the electrical properties of the myocardium, making it effective for treating various cardiac arrhythmias. The drug has minimal effects on repolarization, distinguishing it from Class IA and IB agents.
Approved indications
- Paroxysmal supraventricular tachycardia (PSVT)
- Paroxysmal atrial fibrillation
- Ventricular arrhythmias
Common side effects
- Dizziness
- Dyspnea
- Palpitations
- Chest pain
- Tremor
- Blurred vision
- Nausea
- Proarrhythmic effects
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |