This set of Bepridil hydrochloride MCQs With Answer is crafted for B. Pharm students to strengthen knowledge of bepridil hydrochloride, a non‑selective calcium channel blocker with antiarrhythmic activity. Questions explore mechanism of action, pharmacokinetics, therapeutic uses in supraventricular and ventricular arrhythmias, dosing principles, adverse effects (notably QT prolongation and torsades), drug interactions, contraindications, and monitoring strategies. Focused clinical and pharmaceutical care points—formulation, patient counseling, and emergency management—are emphasized to support exam preparation and real‑world decision making. Now let’s test your knowledge with 30 MCQs on this topic.
Q1. Which pharmacological class best describes bepridil hydrochloride?
- Beta‑adrenergic blocker
- Sodium channel blocker (Class I) only
- L‑type calcium channel blocker with antiarrhythmic properties
- ACE inhibitor
Correct Answer: L‑type calcium channel blocker with antiarrhythmic properties
Q2. What is the primary clinical indication for bepridil hydrochloride?
- Antihypertensive monotherapy
- Management of supraventricular and ventricular arrhythmias
- Chronic heart failure first‑line therapy
- Acute ischemic stroke treatment
Correct Answer: Management of supraventricular and ventricular arrhythmias
Q3. The main mechanism of action of bepridil involves blockade of which channel?
- Voltage‑gated sodium channels exclusively
- L‑type calcium channels reducing AV nodal conduction
- Renal sodium channels increasing diuresis
- H+/K+ ATPase in gastric mucosa
Correct Answer: L‑type calcium channels reducing AV nodal conduction
Q4. Which serious cardiac adverse effect is most associated with bepridil?
- Severe bradycardia without ECG changes
- QT interval prolongation leading to torsades de pointes
- Acute myocardial infarction
- Pulmonary embolism
Correct Answer: QT interval prolongation leading to torsades de pointes
Q5. Which organ plays the major role in the metabolism of bepridil hydrochloride?
- Kidney (renal excretion unchanged)
- Liver (hepatic metabolism)
- Lungs (pulmonary metabolism)
- Skin (cutaneous metabolism)
Correct Answer: Liver (hepatic metabolism)
Q6. Which monitoring parameter is essential when a patient is started on bepridil?
- Regular chest X‑rays
- Serial ECG monitoring for QT interval
- Daily fasting blood glucose only
- Urine protein testing
Correct Answer: Serial ECG monitoring for QT interval
Q7. Bepridil is contraindicated in which of the following conditions?
- Well‑controlled hypertension
- Congenital long QT syndrome
- Mild seasonal allergies
- Hyperthyroidism controlled with medication
Correct Answer: Congenital long QT syndrome
Q8. Concurrent use of bepridil with which drug class increases the risk of torsades de pointes?
- Selective serotonin reuptake inhibitors with QT liability
- Topical antifungals without systemic absorption
- Topical corticosteroids
- Oral probiotics
Correct Answer: Selective serotonin reuptake inhibitors with QT liability
Q9. In a patient developing torsades de pointes while on bepridil, the immediate management includes:
- Oral potassium supplements only
- Intravenous magnesium sulfate and electrical cardioversion if unstable
- Increasing the bepridil dose
- Oral antacids
Correct Answer: Intravenous magnesium sulfate and electrical cardioversion if unstable
Q10. Which hemodynamic effect is commonly observed with bepridil therapy?
- Marked increase in systemic vascular resistance
- Hypotension due to vasodilation
- Severe hypervolemia
- Immediate hypertensive crisis in all patients
Correct Answer: Hypotension due to vasodilation
Q11. Bepridil can exert which effect on myocardial contractility?
- Positive inotropic effect increasing contractility
- Negative inotropic effect potentially reducing contractility
- No effect on contractility ever
- Direct chronotropic stimulation only
Correct Answer: Negative inotropic effect potentially reducing contractility
Q12. The marketed pharmaceutical form is commonly the hydrochloride salt because it:
- Makes the drug lipophilic for topical use
- Improves solubility and stability for oral administration
- Eliminates the need for dosing adjustments
- Makes it inactive until metabolized
Correct Answer: Improves solubility and stability for oral administration
Q13. Which electrolyte disturbance most increases the risk of torsades with bepridil?
- Hypercalcemia
- Hypokalemia
- Hypernatremia
- Alkalosis without electrolyte change
Correct Answer: Hypokalemia
Q14. Co‑administration of bepridil with a strong inhibitor of which metabolic pathway is most likely to raise bepridil plasma levels?
- CYP3A4 inhibitors such as ketoconazole
- Renal organic anion transporter inhibitors only
- Topical enzyme inhibitors
- Monoamine oxidase inhibitors without hepatic effects
Correct Answer: CYP3A4 inhibitors such as ketoconazole
Q15. A common noncardiac adverse effect seen with many calcium channel blockers that may occur with bepridil is:
- Severe pruritus as the most common effect
- Constipation
- Profuse rhinorrhea in all patients
- Hyperglycemia in all cases
Correct Answer: Constipation
Q16. When combining bepridil with other antiarrhythmics, the safest monitoring approach is:
- No monitoring needed if initial ECG is normal
- Frequent ECG and serum electrolyte monitoring
- Only monitor blood pressure at monthly visits
- Rely solely on patient symptom reports
Correct Answer: Frequent ECG and serum electrolyte monitoring
Q17. Why has clinical use of bepridil become limited in many settings?
- Because it is universally ineffective
- Due to risk of severe QT prolongation and torsades de pointes
- Because it causes permanent hair loss
- Because it is prohibitively expensive compared with placebo
Correct Answer: Due to risk of severe QT prolongation and torsades de pointes
Q18. Bepridil’s effect on atrioventricular conduction is most likely to produce which ECG change?
- Marked shortening of PR interval
- Prolongation of PR interval due to slowed AV nodal conduction
- Immediate disappearance of the QRS complex
- Pathognomonic U waves in all patients
Correct Answer: Prolongation of PR interval due to slowed AV nodal conduction
Q19. Patients taking bepridil should be advised to seek immediate care if they experience:
- Mild dry skin that improves with lotion
- Syncope, palpitations or sudden fainting
- Typical seasonal sneezing
- Minor bruising after a bump
Correct Answer: Syncope, palpitations or sudden fainting
Q20. For pharmaceutical handling and storage, bepridil hydrochloride tablets are generally stored:
- Frozen at −20°C
- At controlled room temperature, protected from moisture
- Exposed to direct sunlight to increase potency
- In open containers to allow aeration
Correct Answer: At controlled room temperature, protected from moisture
Q21. Extra caution is required when prescribing bepridil to patients with which cardiac condition?
- Isolated asymptomatic mitral valve prolapse only
- Severe left ventricular systolic dysfunction (heart failure)
- Stable fixed pulmonary stenosis
- Mild, well‑controlled essential tremor
Correct Answer: Severe left ventricular systolic dysfunction (heart failure)
Q22. Which class of antiarrhythmics should generally be avoided with bepridil because of additive QT prolongation?
- Class II beta blockers
- Class IA and Class III antiarrhythmics
- Short‑acting nitrates
- Loop diuretics without QT effects
Correct Answer: Class IA and Class III antiarrhythmics
Q23. Besides ECG monitoring, which laboratory tests are important when a patient is on bepridil?
- Serum electrolytes, especially potassium and magnesium
- Only liver biopsy is required
- Daily complete urine microscopy
- Serum vitamin D levels only
Correct Answer: Serum electrolytes, especially potassium and magnesium
Q24. At the cellular level, bepridil tends to have which effect on cardiac action potentials?
- Shortens action potential duration significantly
- Prolongs action potential duration and repolarization
- Eliminates phase 4 depolarization completely
- Has no effect on action potentials
Correct Answer: Prolongs action potential duration and repolarization
Q25. Which life‑threatening arrhythmia is most directly linked to bepridil toxicity?
- Sinus tachycardia only
- Torsades de pointes (polymorphic ventricular tachycardia)
- Atrial premature complexes that are always benign
- Asymptomatic first‑degree AV block without progression
Correct Answer: Torsades de pointes (polymorphic ventricular tachycardia)
Q26. Part of bepridil’s pharmacological profile includes peripheral vasodilation. This contributes to which clinical effect?
- Worsening angina in all patients
- Reduction in systemic vascular resistance and anti‑anginal benefit
- Increased platelet aggregation
- Direct anticoagulant action
Correct Answer: Reduction in systemic vascular resistance and anti‑anginal benefit
Q27. Bepridil is contraindicated in patients with which degree of AV block unless a pacemaker is present?
- First‑degree AV block only
- Second‑ or third‑degree AV block without a pacemaker
- Bundle branch block without symptoms
- Sinus arrhythmia
Correct Answer: Second‑ or third‑degree AV block without a pacemaker
Q28. Which common dietary interaction may increase bepridil plasma concentrations?
- High‑fiber diet reducing absorption
- Grapefruit juice inhibiting intestinal CYP3A4
- Green leafy vegetables high in vitamin K
- Bananas providing extra potassium
Correct Answer: Grapefruit juice inhibiting intestinal CYP3A4
Q29. Bepridil’s pharmacodynamic profile is most similar to which of the following agents?
- Non‑dihydropyridine calcium channel blockers such as verapamil
- Thiazide diuretics like hydrochlorothiazide
- Direct renin inhibitors only
- Short‑acting insulin analogs
Correct Answer: Non‑dihydropyridine calcium channel blockers such as verapamil
Q30. Before initiating bepridil therapy, which baseline assessments are recommended?
- Baseline ECG and serum electrolytes (K+, Mg2+)
- Only a dermatology consult
- MRI of the brain in all patients
- No baseline tests are necessary
Correct Answer: Baseline ECG and serum electrolytes (K+, Mg2+)

I am a Registered Pharmacist under the Pharmacy Act, 1948, and the founder of PharmacyFreak.com. I hold a Bachelor of Pharmacy degree from Rungta College of Pharmaceutical Science and Research. With a strong academic foundation and practical knowledge, I am committed to providing accurate, easy-to-understand content to support pharmacy students and professionals. My aim is to make complex pharmaceutical concepts accessible and useful for real-world application.
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