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Bactrim iv prophylaxis dose. Antimicrobial activity was measured using a standardized methodology. MAIN METHODS: Cases were enrolled and randomized in an open pilot program during influenza pandemic to receive prophylactic bacitracin 600 mg IV over 5 days. The primary outcome was proportion of eligible cases who survived. Outcome-defined Ultram 200mg 90 pills US$ 260.00 US$ 2.89 groups were defined using pre-defined criteria. RESULTS: This study is the first randomized trial comparing two antimicrobial prophylaxis regimens in an influenza pandemic. The proportion of patients randomized to the three- and six-dose regimen was comparable at day 5 (38% for all groups) (P =.87) and week 5 (39% for groups 1, 2, 3) (P =.73). In the entire study population, incidence of treatment failure was 2.6% for groups 1, 2, 3 and 3.2% for group 1, 4 (P =.29). Infection-free days were similar for all groups at 10, 20, 50 and 80 days (P=.47). After adjustment for baseline differences in age, gender, previous antimicrobial therapy, severity of viral illness, comorbidities, prior therapy with order ultram overnight bactrim and concomitant chemotherapy, the proportion of patients with 50-day infection-free days (ie, without documented clinical manifestations of illness) was higher for group 1 (60.4% or 60.8 for the three-dose group; P =.002; 53.3% or 58.6 for the 6-dose group; P =.01) than ultram for sale overnight for group 2 (31.3% or 36.2 for the three-dose group; P =.03; 21.7% or 24.2 for the six-dose group; P =.04). The 6- and 10-day case-fatality rates remained similar at week 5. The 10-day case-fatality rate remained higher than 2 (12% versus 1%; P =.02) in the three-dose group. CONCLUSION: Results of the three- and six-dose prophylaxis trials were comparable at week 10. The incidence of treatment failure with group 1 was significantly higher after adjustment for baseline differences in age, gender, and severity of viral illness in the two-dose prophylaxis group. 10-day infection-free rate for all three groups was comparable for both patients at week 40. Antibiotics were beneficial for treatment failure with group 1. In the three- and six-dose treatment groups, efficacy buy ultram overnight shipping was maintained throughout influenza season without major adverse effects. CLINICAL TRIAL REGISTRATION No. NCT01441512 and NCT01938641.