Patient information for PROPAFENONE HYDROCHLORIDE 150MG TABLETS Including dosage instructions and possible side effects.
Propafenone hydrochloride is an antiarrhythmic drug
supplied in scored, film-coated tablets of 150, 225 and 300 mg for oral
administration. Propafenone has some structural similarities to
beta-blocking agents.
CLINICAL PHARMACOLOGY
Mechanism of Action
Propafenone is a Class 1C antiarrhythmic drug with
local anesthetic effects, and a direct stabilizing action on myocardial
membranes. The electrophysiological effect of propafenone manifests
itself in a reduction of upstroke velocity (Phase 0) of the monophasic
action potential. In Purkinje fibers, and to a lesser extent myocardial
fibers, propafenone reduces the fast inward current carried by sodium
ions. Diastolic excitability threshold is increased and effective
refractory period prolonged. Propafenone reduces spontaneous
automaticity and depresses triggered activity.
Studies in anesthetized dogs and isolated organ preparations show
that propafenone has beta-sympatholytic activity at about 1/50 the
potency of propranolol. Clinical studies employing isoproterenol
challenge and exercise testing after single doses of propafenone
indicate a beta-adrenergic blocking potency (per mg) about 1/40 that of
propranolol in man. In clinical trials, resting heart rate decreases of
about 8% were noted at the higher end of the therapeutic plasma
concentration range. At very high concentrations in vitro,
propafenone can inhibit the slow inward current carried by calcium, but
this calcium antagonist effect probably does not contribute to
antiarrhythmic efficacy. Propafenone has local anesthetic activity
approximately equal to procaine.Electrophysiology
Electrophysiology studies in patients with ventricular
tachycardia (VT) have shown that propafenone HCl prolongs
atrioventricular (AV) conduction while having little or no effect on
sinus node function. Both AV nodal conduction time (AH interval) and
His-Purkinje conduction time (HV interval) are prolonged. Propafenone
has little or no effect on the atrial functional refractory period, but
AV nodal functional and effective refractory periods are prolonged. In
patients with Wolff-Parkinson-White (WPW) syndrome, propafenone reduces
conduction and increases the effective refractory period of the
accessory pathway in both directions. Propafenone slows conduction and
consequently produces dose-related changes in the PR interval and QRS
duration. QTc interval does not change.
INDICATIONS AND USAGE
In patients without structural heart disease, propafenone is indicated to prolong the time to recurrence of
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- paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.
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- paroxysmal supraventricular tachycardia (PSVT) associated with disabling symptoms.
The use of propafenone HCl in patients with chronic atrial fibrillation has not been evaluated. Propafenone HCl should not be used to control ventricular rate during atrial fibrillation.
Propafenone HCl is also indicated for the treatment of
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- documented ventricular arrhythmias, such as sustained ventricular tachycardia, that, in the judgment of the physician, are life-threatening. Because of the proarrhythmic effects of propafenone HCl, its use with lesser ventricular arrhythmias is not recommended, even if patients are symptomatic, and any use of the drug should be reserved for patients in whom, in the opinion of the physician, the potential benefits outweigh the risks.
Propafenone HCl, like other antiarrhythmic drugs, has not been shown to enhance survival in patients with ventricular or atrial arrhythmias.
CONTRAINDICATIONS
Propafenone HCl is contraindicated in the presence of
uncontrolled congestive heart failure, cardiogenic shock, sinoatrial,
atrioventricular and intraventricular disorders of impulse generation
and/or conduction (e.g., sick sinus node syndrome, atrioventricular
block) in the absence of an artificial pacemaker, bradycardia, marked
hypotension, bronchospastic disorders, manifest electrolyte imbalance,
and known hypersensitivity to the drug.
