To the Editor: In this issue of the Journal, Black et al.1 reporton a significant increase in the risk of serious atrial-fibrillationadverse events (defined as events resulting in hospitalizationor disability or judged to be life-threatening) associated withonce-yearly infusions of intravenous zoledronic acid for thetreatment of osteoporosis in postmenopausal women. However,there was no increased risk of all adverse events of atrialfibrillation with such infusions.
We reviewed the results of the Fracture Intervention Trial (FIT),a randomized study of alendronate sponsored by Merck, whichinvolved 6459 postmenopausal women (mean age, 69 years).2,3The University . . . [Full Text of this Article]
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