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Merck

Weekly fluconazole therapy for recurrent vulvovaginal candidiasis: a systematic review and meta-analysis.

European journal of obstetrics, gynecology, and reproductive biology (2013-01-03)
Maria I Rosa, Bruno R Silva, Patrícia S Pires, Fábio R Silva, Napoleão C Silva, Fábio R Silva, Suéli L Souza, Kristian Madeira, Ana P Panatto, Lidia R Medeiros
RESUMEN

To investigate the efficacy, compared to placebo, of fluconazole 150 mg weekly, given for six months as prophylaxis against recurrent vulvovaginal candidiasis (RVVC). A quantitative systematic review was performed, and randomized controlled trials were included. We conducted searches at Medline, EMBASE, Lilacs, Cochrane Library and ICI Web of Science from 1980 to March 2012. We used the odds ratio (OR) with confidence intervals (CI) of 95% using a random effects model of Mantel-Haenszel. The software used was Review Manager version 5.0. Through the search strategies we identified 249 articles, of which only two were part of the meta-analysis. Fluconazole was more effective than placebo in reducing symptomatic episodes of VVC, immediately after treatment (OR 0.10, 95% CI 0.03-0.34), 3 months after treatment (OR 0.23, 95% CI 0.07-0.74) and 6 months after treatment (OR 0.39, 95% CI 0.24-0.64). Weekly treatment with fluconazole (150 mg) for six months is effective against RVVC.

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Sigma-Aldrich
Fluconazole, ≥98% (HPLC), powder
USP
Fluconazole, United States Pharmacopeia (USP) Reference Standard
Supelco
Fluconazole, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Fluconazole solution, 2.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Fluconazole, European Pharmacopoeia (EP) Reference Standard
Fluconazole for peak identification, European Pharmacopoeia (EP) Reference Standard