CHLORAMPHENICOL
Outline

Copyright, Purdue Research Foundation, 1996

| BMS 445 Intro | | Drug Groups | | Slides / Graphics | | Address | | E-mail | | full |


Overview

Structure and chemical characteristics

Mechanism of action

Resistance

Pharmacokinetics

Adverse Effects

Allergic

Biological effects

Direct toxicity

Reversible, dose-related anemia

Idiosyncratic blood dyscrasias

Teratogenesis

Gray Baby Syndrome

Drug interaction

Clinical applications

References

Study Questions

  1. Note the low water solubilitiy of chloramphenicol base and it high lipid solubility. Given that protein binding is moderate (meaning not much of a factor), predict its bioavailability after oral administration (assuming no biotransformation) and the relation between its plasma and intracellular concentrations (CSF, too).
  2. Why must chloramphenicol not be used in food producing animals?
  3. How does the antimicrobial (As opposed to antibacterial) spectrum of chloramphenicol differ from that of the tetracyclines?
  4. How does the mechanism of action of chloramphenicol compare to that of the aminoglycosides and beta-lactams?
  5. What is the major route of elimination of chloramphenicol? How do poor renal function and poorly developed biotransforming enzymes and elimination\lr<120> systems affect chloramphenicol toxicity? Name a condition in neonates that stems from these deficiencies and failure to properly adjust dosage.
  6. What is the major adverse effects of chloramphenicol that limits its use?

    | Drug Groups | | top |
    Gordon L. Coppoc, DVM, PhD
    Professor of Veterinary Pharmacology
    Head, Department of Basic Medical Sciences
    School of Veterinary Medicine
    Purdue University
    West Lafayette, IN 47907-1246
    Tel: 317-494-8633Fax: 317-494-0781
    Email: coppoc@vet.purdue.edu

    Last modified
    9:56 PM on 4/15/96
    GLC