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Question 446

Pharmacology → General

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Destination Site
Type SSBA
UUID 8bfe877a-aff0-42a8-a592-2a93d562f918

Classification

Speciality
Obstetrics and Gynaecology
Group
Basic
Title
Pharmacology
Topic
General
Subtopic 1
Clinical Pharmacy
Subtopic 2
Hepatic enzyme activity
Subtopic 3
Induction and inhibition
Question Type
SBA

Question

SSBA
Question Header
A drug whose clearance depends substantially on hepatic microsomal metabolism is given with a second agent. Which pairing would be expected to exert opposing effects on hepatic microsomal enzyme activity?
Question Stem
Select the single best answer.

Options

A Phenytoin and carbamazepine
B Rifampicin and phenobarbitone
C Erythromycin and fluconazole
D Carbamazepine and erythromycin
E Cimetidine and ketoconazole

Explanation

Carbamazepine induces hepatic microsomal enzymes, whereas erythromycin inhibits them. Co-administration therefore introduces opposing influences on microsomal drug metabolism. Phenytoin, rifampicin and phenobarbitone are also enzyme inducers, whereas fluconazole, cimetidine and ketoconazole are enzyme inhibitors.

Option Validity

A) Both phenytoin and carbamazepine are hepatic microsomal enzyme inducers.

B) Both rifampicin and phenobarbitone are enzyme inducers.

C) Erythromycin and fluconazole are both listed as enzyme inhibitors.

E) Cimetidine and ketoconazole are both listed as enzyme inhibitors.

Further Reading

Saxena R. Textbook for MRCOG-1. Chapter 12: Pharmacology. Clinical Pharmacy, pp.344–345.

Source & metrics

Authored Difficulty
5.00
Evaluation Score
—
Destination
Site
Source
Saxena - MRCOG-1 Basic Sciences - Pharmacology - General
Source Section
Clinical Pharmacy
Source Locator
Chapter 12, pp.344–345
Updated
2026-10-06 01:57:35
Difficulty Factor
Not available yet
Attended Users
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