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Propafenone i.v.

Charles University, Czech Republic · FDA-approved active Small molecule Under review

Propafenone i.v. is a Class IC antiarrhythmic agent Small molecule drug developed by Charles University, Czech Republic. It is currently FDA-approved for Atrial fibrillation (maintenance of sinus rhythm), Paroxysmal supraventricular tachycardia, Ventricular arrhythmias. Also known as: Antiarrhythmic therapy.

Propafenone is a Class IC antiarrhythmic agent that blocks cardiac sodium channels to slow conduction velocity and suppress abnormal electrical activity in the heart.

Propafenone i.v. is used to treat supraventricular arrhythmia and septic shock, as per clinical trials. Its mechanism of action is as a class Ic antiarrhythmic agent, according to ChEMBL.

At a glance

Generic namePropafenone i.v.
Also known asAntiarrhythmic therapy
SponsorCharles University, Czech Republic
Drug classClass IC antiarrhythmic agent
TargetCardiac sodium channel (Nav1.5)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Propafenone inhibits the fast inward sodium current in cardiac tissue, which decreases the rate of depolarization and slows conduction through the atria and ventricles. This sodium channel blockade also has weak beta-blocking and calcium channel blocking properties. The net effect is suppression of ectopic arrhythmias and stabilization of abnormal cardiac rhythms.

Approved indications

Common side 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.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about Propafenone i.v.

What is Propafenone i.v.?

Propafenone i.v. is a Class IC antiarrhythmic agent drug developed by Charles University, Czech Republic, indicated for Atrial fibrillation (maintenance of sinus rhythm), Paroxysmal supraventricular tachycardia, Ventricular arrhythmias.

How does Propafenone i.v. work?

Propafenone is a Class IC antiarrhythmic agent that blocks cardiac sodium channels to slow conduction velocity and suppress abnormal electrical activity in the heart.

What is Propafenone i.v. used for?

Propafenone i.v. is indicated for Atrial fibrillation (maintenance of sinus rhythm), Paroxysmal supraventricular tachycardia, Ventricular arrhythmias.

Who makes Propafenone i.v.?

Propafenone i.v. is developed and marketed by Charles University, Czech Republic (see full Charles University, Czech Republic pipeline at /company/charles-university-czech-republic).

Is Propafenone i.v. also known as anything else?

Propafenone i.v. is also known as Antiarrhythmic therapy.

What drug class is Propafenone i.v. in?

Propafenone i.v. belongs to the Class IC antiarrhythmic agent class. See all Class IC antiarrhythmic agent drugs at /class/class-ic-antiarrhythmic-agent.

What development phase is Propafenone i.v. in?

Propafenone i.v. is FDA-approved (marketed).

What are the side effects of Propafenone i.v.?

Common side effects of Propafenone i.v. include Dizziness, Headache, Nausea, Blurred vision, Proarrhythmic effects, Bradycardia.

What does Propafenone i.v. target?

Propafenone i.v. targets Cardiac sodium channel (Nav1.5) and is a Class IC antiarrhythmic agent.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing