Introduction |
Macrolides are a large group of anti microbials derived from Streptomyces spp. With low toxicity exhibiting bacteriostatic and bactericidal(against some) effects through inhibition of bacterial RNA dependent protein synthesis by binding to 50S ribosomal subunit and some times manifesting cross resistance among them. The antimicrobial spectrum is similar to benzyl penicillin but in addition active against Mycoplasmae, Chlamydiae, Legionellae, gram positive anaerobes etc.. The newer agents like clarithromycin, Azithromycin, Dirithromycin are found to be effective against pathogens implicated in opportunistic infections associated with AIDS like MAC infection, Toxoplasmosis, Cryptosporidiosis etc., and also in the eradication of H.pylori infection and in Lyme disease caused by B.burgedorferi. Macrolides like Spiramycin, Kitasamycin, Josamycin and Medicamycin, Miocamycin and Rokitamycin are widely used in Japan & Europe. Erythromycin, Azithromycin and Spiramycin can safely be used in PREGNANCY. Among the Macrolides Azithromycin, Dirithromycin and Spiramycin does not interfere with CYP3A isoenzyme and therefore NO drug interactions as seen with clarithromycin. |
Macrolides have additional pharmacological actions not connected with their antimicrobial actions on the following receptors: |
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Clarithromycin is a semi synthetic broad spectrum macrolide antimicrobial agent having not only bactericidal activity against some organisms by virtue of its synergism with its microbiologically active 14 OH metabolite but also by its Post Antibiotic Effect (PAE). |
Current Review focuses antimicrobial activity, Clinical pharmacokinetics, efficacy, tolerability & safety profiles, and pharmacoeconomic considerations of clarithromycin. The concluding topic of “Choosing Macrolides” has been added for the benefit of readers. |
CLARITHROMYCIN
CLARITHROMYCIN
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