To the Editor: In his letter (Sept. 15 issue),1 Huston describedbilateral rupture of the Achilles tendon in a patient treatedwith enoxacin and prednisone. Although no cases of tendon rupturewere reported to the Food and Drug Administration (FDA) duringpremarketing clinical trials of fluoroquinolones currently onthe market, the following information from the FDA's PostmarketingSpontaneous Reporting System does support the need for increasedawareness of this adverse event.
As of October 1994, 25 cases of tendon rupture were reported,22 of them occurring outside the United States. The patientswhose ages were reported ranged from 33 to . . . [Full Text of this Article]
References
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