Ethambutol – mechanism of action MCQs With Answer
Ethambutol is a first-line antitubercular agent important for B.Pharm students to understand, particularly its mechanism of action and clinical implications. It is a bacteriostatic inhibitor of mycobacterial cell wall biosynthesis that targets arabinosyl transferases (Emb proteins), blocking arabinogalactan polymerization and weakening the mycobacterial cell envelope. Key topics include dosing, pharmacokinetics, renal excretion, resistance mechanisms (embB mutations), and dose-related ocular toxicity such as optic neuritis and color vision defects. Familiarity with monitoring (visual acuity, Ishihara plates), dose adjustment in renal impairment, and its role in combination therapy (RIPE regimen) is essential.
Now let’s test your knowledge with 30 MCQs on this topic.
Q1. What is the primary mechanism of action of ethambutol against Mycobacterium tuberculosis?
- Inhibition of mycolic acid synthesis by targeting FAS-II enzymes
- Inhibition of arabinosyl transferase enzymes blocking arabinogalactan polymerization
- Disruption of DNA gyrase leading to DNA strand breaks
- Inhibition of protein synthesis at the 30S ribosomal subunit
Correct Answer: Inhibition of arabinosyl transferase enzymes blocking arabinogalactan polymerization
Q2. Ethambutol is classified pharmacodynamically as which of the following against M. tuberculosis?
- Bactericidal
- Bacteriostatic
- Fungistatic
- Virucidal
Correct Answer: Bacteriostatic
Q3. Which cell wall component synthesis is directly affected by ethambutol?
- Peptidoglycan cross-linking
- Arabinogalactan polymerization
- Mycolic acid condensation
- Lipooligosaccharide formation
Correct Answer: Arabinogalactan polymerization
Q4. Mutations in which gene are most commonly associated with ethambutol resistance?
- katG
- rpoB
- embB
- gyrA
Correct Answer: embB
Q5. What is the usual recommended adult dose of ethambutol in daily tuberculosis therapy?
- 5 mg/kg once daily
- 15 mg/kg once daily
- 50 mg/kg once daily
- 100 mg once weekly
Correct Answer: 15 mg/kg once daily
Q6. Which of the following is the most clinically important adverse effect of ethambutol?
- Hepatotoxicity with transaminase elevation
- Severe neutropenia
- Optic neuritis with decreased visual acuity and color vision defects
- Ototoxicity with hearing loss
Correct Answer: Optic neuritis with decreased visual acuity and color vision defects
Q7. What baseline and periodic monitoring is essential for patients on ethambutol?
- Liver function tests monthly
- Serum creatinine and electrolytes weekly
- Visual acuity and color vision testing at baseline and monthly
- Complete blood count daily
Correct Answer: Visual acuity and color vision testing at baseline and monthly
Q8. How is ethambutol primarily eliminated from the body?
- Hepatic metabolism followed by biliary excretion
- Renal excretion, largely unchanged
- Respiratory elimination via exhaled air
- Metabolism to active metabolites in the gut
Correct Answer: Renal excretion, largely unchanged
Q9. What adjustment is required for ethambutol in severe renal impairment?
- No adjustment needed; give standard dose
- Increase dose frequency to twice daily
- Reduce dose or extend dosing interval due to decreased clearance
- Switch to intravenous formulation
Correct Answer: Reduce dose or extend dosing interval due to decreased clearance
Q10. Which visual defect is classically associated with ethambutol toxicity?
- Blue-yellow color blindness
- Central scotoma without color change
- Red-green color vision impairment
- Peripheral tunnel vision only
Correct Answer: Red-green color vision impairment
Q11. Ethambutol is commonly included in which first-line anti-TB regimen acronym?
- MAZE regimen
- RIPE regimen
- PARM regimen
- DOTS-Plus regimen only
Correct Answer: RIPE regimen
Q12. Which Emb proteins are primary molecular targets of ethambutol?
- EmbX and EmbY
- EmbA, EmbB and EmbC
- Emb1 and Emb2 only
- EmbM and EmbN
Correct Answer: EmbA, EmbB and EmbC
Q13. Which diagnostic test is most appropriate for routine color vision monitoring in patients on ethambutol?
- Snellen chart only
- Ishihara color plates
- Electroretinogram (ERG) monthly
- Visual evoked potentials weekly
Correct Answer: Ishihara color plates
Q14. In the mechanism of ethambutol, inhibition of arabinosyl transferases primarily interferes with which linkage in the mycobacterial cell envelope?
- Peptidoglycan-peptide crosslinking
- Attachment and polymerization of arabinogalactan to the cell wall
- Synthesis of trehalose dimycolate
- Glycolipid transport across membrane
Correct Answer: Attachment and polymerization of arabinogalactan to the cell wall
Q15. The most common molecular mechanism by which Mycobacterium acquires resistance to ethambutol is:
- Overexpression of efflux pumps only
- Mutation in embB leading to altered arabinosyl transferase
- Plasmid-mediated enzymatic inactivation
- Increased cell wall permeability
Correct Answer: Mutation in embB leading to altered arabinosyl transferase
Q16. Which statement about ethambutol pharmacokinetics is correct?
- It is extensively metabolized by CYP3A4 into active metabolites
- It has poor oral absorption and must be given IV
- It is well absorbed orally and largely excreted unchanged by kidneys
- It is secreted into bile and reabsorbed enterohepatically
Correct Answer: It is well absorbed orally and largely excreted unchanged by kidneys
Q17. Which of the following statements about ethambutol use in pregnancy is most accurate?
- Contraindicated due to teratogenicity
- Generally considered safe and can be used if benefit outweighs risk
- Requires routine fetal vision screening during therapy
- Should be replaced by streptomycin in all pregnant patients
Correct Answer: Generally considered safe and can be used if benefit outweighs risk
Q18. Which of the following clinical signs would most likely prompt immediate discontinuation of ethambutol?
- Transient mild nausea
- Significant new decrease in visual acuity and color vision
- Elevated ALT twice the normal limit with no symptoms
- Mild peripheral neuropathy after one dose
Correct Answer: Significant new decrease in visual acuity and color vision
Q19. Ethambutol’s antibacterial spectrum primarily includes:
- Typical Gram-positive cocci only
- Many Gram-negative rods but not mycobacteria
- Mycobacteria including M. tuberculosis and some atypical mycobacteria
- Fungi and certain protozoa
Correct Answer: Mycobacteria including M. tuberculosis and some atypical mycobacteria
Q20. Which laboratory method is commonly used to measure plasma ethambutol concentrations in research or therapeutic monitoring?
- High-performance liquid chromatography (HPLC)
- Complete blood count
- Western blot assay
- Microscopy with Ziehl-Neelsen stain
Correct Answer: High-performance liquid chromatography (HPLC)
Q21. Risk of ethambutol-induced optic neuritis is most strongly correlated with which factor?
- Concurrent use of pyrazinamide
- Higher daily doses and prolonged duration
- Patient age under 5 years only
- Administration with food
Correct Answer: Higher daily doses and prolonged duration
Q22. How should ethambutol be dosed in pediatric patients?
- Same flat adult dose irrespective of weight
- Weight-based dosing, commonly 15–25 mg/kg once daily with careful monitoring
- Only once weekly dosing at 100 mg/kg
- Not recommended at any pediatric age
Correct Answer: Weight-based dosing, commonly 15–25 mg/kg once daily with careful monitoring
Q23. Which organ system is the primary target of ethambutol toxicity?
- Hepatic system
- Renal glomeruli
- Visual/optic nerve system
- Cardiac conduction system
Correct Answer: Visual/optic nerve system
Q24. When ethambutol-induced optic neuritis is suspected, the immediate management should be:
- Reduce the dose by half and continue therapy
- Stop ethambutol immediately and perform ophthalmologic evaluation
- Ignore mild symptoms and continue treatment for full course
- Switch to a fluoroquinolone without further testing
Correct Answer: Stop ethambutol immediately and perform ophthalmologic evaluation
Q25. Ethambutol’s inclusion in combination TB therapy primarily helps to:
- Prevent hepatotoxicity caused by isoniazid
- Reduce the emergence of resistance by targeting a different cell wall pathway
- Act as the sole sterilizing agent against dormant bacilli
- Provide rapid symptomatic relief of cough
Correct Answer: Reduce the emergence of resistance by targeting a different cell wall pathway
Q26. Which of the following decreases ethambutol absorption when administered concomitantly?
- Strong acidic beverages
- Antacids containing aluminum or magnesium
- Vitamin C supplements
- Proton pump inhibitors increase absorption markedly
Correct Answer: Antacids containing aluminum or magnesium
Q27. Ethambutol’s half-life in patients with normal renal function is approximately:
- 30 minutes
- 3–4 hours
- 24–48 hours
- 7–10 days
Correct Answer: 3–4 hours
Q28. Which clinical feature differentiates ethambutol optic neuritis from other ocular conditions?
- Predominant blue-yellow dyschromatopsia only
- Painless progressive loss of central vision with red-green dyschromatopsia
- Severe eye pain with photophobia
- Acute proptosis and conjunctival hemorrhage
Correct Answer: Painless progressive loss of central vision with red-green dyschromatopsia
Q29. In the lab, ethambutol-resistant M. tuberculosis is most likely to show which phenotypic change?
- Increased susceptibility to isoniazid
- Growth on media containing ethambutol concentrations that inhibit wild-type strains
- Loss of acid-fast staining properties
- Complete inability to grow on synthetic media
Correct Answer: Growth on media containing ethambutol concentrations that inhibit wild-type strains
Q30. For a patient who develops mild reversible ethambutol optic neuritis after 4 weeks, what is the expected course after stopping the drug?
- Progressive irreversible blindness despite stopping drug
- Gradual improvement of vision over weeks to months in many cases
- Immediate complete recovery within 24 hours
- No change; vision remains the same permanently
Correct Answer: Gradual improvement of vision over weeks to months in many cases

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.
Mail- Sachin@pharmacyfreak.com