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The following outcomes were the clinical cure rates at the Day 21 to 24 visit for the bacteriologically evaluable patients by pathogen: In the safety analysis of this study, the incidence of treatment-related adverse events, primarily gastrointestinal, were comparable between treatment arms (25% with azithromycin and 29% with clarithromycin)
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Potentially dilutive securities that were not included in the diluted per share calculations because they would be anti-dilutive were as follows: Note 12
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