Chloramphenicol is a bacteriostatic broad-spectrum antibiotic that is active against both aerobic and anaerobic gram-positive and gram-negative organisms. It is active also against rickettsiae. Haemophilus influenzae, N. meningitidis, and some strains of Bacteroides are highly susceptible, and for them chloramphenicol may be bactericidal. Clinically significant resistance emerges and may be due to production of chloramphenicol acetyltransferase, an enzyme that inactivates the drug.
Pharmacokinetics: Following oral administration, chloramphenicol is rapidly and completely absorbed. It is widely distributed to virtually all tissues and body fluids. The drug penetrates cell membranes readily. Excretion of active chloramphenicol and of inactive degradation products occurs by way of the urine. A small amount of active drug is excreted into bile or feces. Newborns less than a week old and premature infants clear chloramphenicol inadequately.
Clinical Uses: Because of potential toxicity, bacterial resistance, and the availability of other effective drugs, chloramphenicol may be considered mainly for treatment of serious rickettsial infections, bacterial meningitis caused by a markedly penicillin-resistant strain of pneumococcus or meningococcus, and thyphoid fever.
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