Effect of fluconazole on zidovudine pharmacokinetics in patients infected with human immunodeficiency virus
- PMID: 8169401
- DOI: 10.1093/infdis/169.5.1103
Effect of fluconazole on zidovudine pharmacokinetics in patients infected with human immunodeficiency virus
Abstract
The effect of a therapeutic dose of fluconazole on the disposition of zidovudine was evaluated in 12 men infected with human immunodeficiency virus. The study was designed as a randomized, two-period, two-treatment, crossover trial. On two occasions, 21 days apart, patients received either zidovudine alone or zidovudine (each, 200 mg every 8 h) and fluconazole (400 mg daily) for 7 days. Fluconazole coadministration decreased (P < .001) the apparent oral serum clearance of zidovudine by 43% and the apparent oral formation clearance to zidovudine glucuronide (GZDV) by 48%, resulting in increases (P < .002) in the area under the serum concentration time curve (74%), the maximum serum concentration (84%), and the terminal half-life (128%) of zidovudine. The molar ratio of GZDV to zidovudine recovered in urine was reduced by 34% with fluconazole (P < .001). These pharmacokinetic changes suggest that 400 mg of fluconazole inhibited the conversion of zidovudine to GZDV. Patients receiving this combination should be monitored for the development of zidovudine-related adverse reactions.
Comment in
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Effect of azoles on the glucuronidation of zidovudine by human liver UDP-glucuronosyltransferase.J Infect Dis. 1995 Dec;172(6):1634-6. doi: 10.1093/infdis/172.6.1634. J Infect Dis. 1995. PMID: 7594735 No abstract available.
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