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Pharmacology

Macrolides, tetracyclines, lincosamides and oxazolidinones

Ribosomal targets, spectrum, resistance and the mechanism-based adverse effects and interactions of macrolides, tetracyclines, clindamycin and linezolid, including QT prolongation, CYP3A4 inhibition, toxin suppression and serotonin toxicity.

Tier 2Medical sciences concept

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3 questions9 flashcards

At a glance

  • All four classes bind the bacterial ribosome. Tetracyclines bind the 30S subunit; macrolides, lincosamides (clindamycin) and oxazolidinones (linezolid) bind the 50S subunit. Most are bacteriostatic.
  • Human ribosomes are 80S, which gives selectivity. Mitochondrial ribosomes are bacterial in origin, which explains linezolid's marrow, nerve and lactate toxicity with long courses.
  • The examinable adverse effects follow from mechanism: QT prolongation and CYP3A4 inhibition with macrolides, chelation and photosensitivity with tetracyclines, C. difficile with clindamycin, and serotonin toxicity with linezolid.

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Last updated
14 November 2026
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