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Primarily on the basis of case reports submitted to the FDA's Adverse Event Reporting Program, the agency recently required a change in the labeling of fluoroquinolone antibiotics to include a warning about increased risk for polyneuropathy associated with these drugs (NEJM JW Neurol Aug 29 2013). However, no data have been available to quantify this risk. Now, a case-control study sheds some light on this question. Using health claims data from the LifeLink database (which only includes data from men), investigators identified 6226 incident cases (defined as those with a first physician visit for idiopathic polyneuropathy) and 24,904 age- and disease duration–matched controls and compared the frequency of fluoroquinolone use in each group.…