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Culture was repeated on day The primary study end points were clinical and bacteriologic efficacy assessed on day 12, and clinical and bacteriologic recurrence rates assessed at a visit taking place up to 3 months after the completion of treatment. Tolerability was the secondary end point. Seven hundred seventy-four patients with acute, recurrent GABHS pharyngotonsillitis were enrolled in the study mean age, 28 years; age range, years. There were no significant differences between groups at baseline. No clinical response was observed in the absence of bacteriologic eradication.
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Uses: Serious infections caused by susceptible organisms : -Staphylococci, streptococci, and pneumococci, including serious respiratory tract infections and skin and soft tissue infections -Anaerobes, including serious respiratory tract infections, serious skin and soft tissue infections, septicemia, intraabdominal infections, and infections of the female pelvis and genital tract. Oral : Body weight 10 kg or less: Minimum recommended dose
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