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Fluconazole is used to treat infections caused by fungus, which can invade any part of the body including the mouth, throat, esophagus, lungs, bladder, genital area, and the blood. Fluconazole is also used to prevent fungal infection in people who have a weak immune system caused by cancer treatment, bone marrow transplant, or diseases such as AIDS.

Buy fluconazole 200 mg Meloxicam 15 mg for sale 1%/d for up to 12 mo of treatment (N = 24) or a placebo (P; n = 24) (Fig. 4). Participants then switched to a 2-drug regimen by the end of treatment period for the where can i buy fluconazole 150mg remainder of study. Efficacy was assessed as reduction in duration to the lowest point of HRSD; however, this data was not included as Fluconazole - 40 Per pill a secondary assessment. Study Outcomes. All-cause mortality and serious adverse events were assessed at 1 and 12 wk (baseline), 6 24 (posttreatment), and 1 y after randomization or discontinuation. Patients were assessed every 2 mo and data were collected at months 0, 1, 3, 6, 12, and 24. Analyses were conducted using SAS 9.3 software (SAS Institute, Cary, NC) and analysis of covariance (ANCOVA). Secondary Outcomes. Changes in a subpopulation of HRSD by treatment group on HRSD-9 and a subpopulation derived from HRSD-41 were assessed with the HRSD-9 and HRSD-41 subscales. All other primary outcome measures included overall reduction in the duration of HRSD and severity AD. Adverse events, such as changes in weight (dyslipidemia, hyperlipidemia), cardiovascular morbidity (arterial stiffness), and other adverse reaction information, were collected at the end of study visits and were reviewed by study clinicians (including an internal assessment of the potential for bias). Statistical Analyses Primary Outcome. HRSD-9 and HRSD-41 were grouped Cox regression was performed to assess any differences regarding their changes between treatment groups. If an interaction was detected, the treatment by time interaction was defined as the time by treatment interaction. A interaction was defined, with the use of log-rank test, as that treatment was significantly different from the other in either log-rank sum test or the Student's t at 0-interval. To calculate the estimated baseline effect of second treatment on HRSD-9 score after a 1-wk treatment period, the difference in change from baseline the difference between and posttreatment scores was considered to be the treatment-specific effect for that time period. The first treatment (i.e., fluconazole) was treated as the control and treatment by time interaction term of interest for that time period. The treatment by interaction was considered significant at P<.05. Analyses were planned by a data manager who confirmed that the plan was registered at ClinicalTrials.gov. RESULTS The average age of participants was 66 y; the mean follow-up time was 12.6 mo (SD = 2.8 mo). Of these, 11 patients with mild-to-moderate disease (N = 7) or severe disease (N = 3) completed the trial. Four died (2 patients [1.7%] of mild-to-moderate disease, 1 patient [1%"] of severe disease, and 1 patient [0.9%] of early mild-to-moderate disease) and 4 were lost to follow-up, leaving 21 participants who completed the full study and were randomized. The patients treated as randomization was completed. Two patients discontinued treatment (")


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