Concerning dofetilide pharmacokinetics and dosing, choose the correct statement(s).
Most of the drug (about 75%) is excreted by the kidney, suggesting the need to adjust doses according to creatinine clearance values.
About 25% of dofetilide is subject to cytochrome P450 metabolism, involving mainly the CYP3A4 isoform.
Agents inhibiting this CYP3A4 isoform (e.g. verapamil) may result in higher serum dofetilide levels.
A & B
A, B & C
Choose the correct statement(s) concerning clinical usage and clinical characteristics of dofetilide.
Dofetilide is a negative inotropic drug, therefore depressing ventricular contractility.
Dofetilide is useful in treating atrial fibrillation.
Dofetilide is useful in treating atrial flutter.
A & B
A & C
B & C
A, B & C
Dofetilide may be effective and safely used for atrial fibrillation conversion and recurrence prevention even in patients with congestive heart failure.
True
False
Choose the correct statement(s) concerning dofetilide adverse effects
.Dofetilide administration is associated with about a 3%-4% incidence of torsades de pointes.
Dofetilide probably should be avoided in those patients showing substantial renal dysfunction.
Dofetilide administration should be avoided in patients exhibiting a baseline QT prolongation.
All of the above
Dronedarone exhibit similar electrophysiological properties as this agent:
Ibutilide
Esmolol
Amiodarone
Diltiazem
Dronedarone has been approved for treatment of which one(s) of the following arrhythmias?
Atrial fibrillation
Atrial flutter
Both
Neither
Following oral administration, bioavailability of Dronedarone is about 15%-20%. Which one(s) of the following additional Dronedarone characteristics is/are correct?