The Food and Drug Administration on Tuesday toughened a warning it made last year about the potential risks of azithromycin, a commonly used antibiotic that can cause changes in the electrical activity of the heart that may lead to a fatal irregular heart rhythm in some patients.
The risks, which have been noted in the warning labels on the drug since March 2012, were quantified in greater detail in a study published last spring in the New England Journal of Medicine that was led by a professor of preventive medicine at Vanderbilt University.
Last May, the F.D.A. announced that it would review the study, which found a small increase in the likelihood of death in people treated with a five-day course of azithromycin, compared with people treated with other antibiotics, such as amoxicillin and ciprofloxacin. Two related antibiotics, erythromycin and clarithromycin, were already known to raise the risk of death, but azithromycin had been thought to be safe
The risks, which have been noted in the warning labels on the drug since March 2012, were quantified in greater detail in a study published last spring in the New England Journal of Medicine that was led by a professor of preventive medicine at Vanderbilt University.
Last May, the F.D.A. announced that it would review the study, which found a small increase in the likelihood of death in people treated with a five-day course of azithromycin, compared with people treated with other antibiotics, such as amoxicillin and ciprofloxacin. Two related antibiotics, erythromycin and clarithromycin, were already known to raise the risk of death, but azithromycin had been thought to be safe
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