Which drug is an example of a Class IV antiarrhythmic (calcium channel blocker)?

Prepare for the Rasmussen Pharmacology Exam 3. This quiz includes multiple-choice questions with hints and explanations. Review essential pharmacological concepts and get ready for your exam!

Multiple Choice

Which drug is an example of a Class IV antiarrhythmic (calcium channel blocker)?

Explanation:
Class IV antiarrhythmics are calcium channel blockers that primarily slow conduction through the AV node by blocking L-type calcium channels. This reduces AV nodal conduction velocity and increases the nodal refractory period, which helps control heart rate during atrial tachyarrhythmias such as atrial fibrillation or flutter with rapid ventricular response. Diltiazem is a nondihydropyridine calcium channel blocker that acts on cardiac tissue to slow AV conduction and lower heart rate, making it a textbook example of a Class IV agent. The other drugs listed do not belong to this class. Amiodarone is mainly a Class III agent (potassium channel blockade with many other effects), Lidocaine is a Class Ib sodium channel blocker used for ventricular arrhythmias, and Propranolol is a Class II beta-blocker that reduces AV conduction via adrenergic blockade.

Class IV antiarrhythmics are calcium channel blockers that primarily slow conduction through the AV node by blocking L-type calcium channels. This reduces AV nodal conduction velocity and increases the nodal refractory period, which helps control heart rate during atrial tachyarrhythmias such as atrial fibrillation or flutter with rapid ventricular response. Diltiazem is a nondihydropyridine calcium channel blocker that acts on cardiac tissue to slow AV conduction and lower heart rate, making it a textbook example of a Class IV agent.

The other drugs listed do not belong to this class. Amiodarone is mainly a Class III agent (potassium channel blockade with many other effects), Lidocaine is a Class Ib sodium channel blocker used for ventricular arrhythmias, and Propranolol is a Class II beta-blocker that reduces AV conduction via adrenergic blockade.

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