Evaluation of the safety of macrolides
1University of London, 31 St. Olav's Court, 25 Lower Road, London SE16 2XB, UK. jdw@ischemo.demon.co.uk
Abstract:
The safety of all drugs is established by animal studies, administration to healthy volunteers and the observations during clinical studies to confirm efficacy. During these studies, patients are questioned about side-effects and extensive laboratory testing of blood and urine samples is performed. Despite these extensive studies, new problems may arise during post marketing surveillance which is designed to identify any rare side-effects. Today, all studies suggest that macrolides, and especially the more recently developed agents, are well tolerated. Some variations in tolerability may be due to the size of the macrocyclic ring and the presence of different esters. There are very few instances of irreversible organ damage.
Related Concept Videos
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations
Rocky Mountain Spotted Fever
Mechanism of Antibiotic Resistance in MRSA
Clinical Significance of Antibiotic Resistance


