Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1993 Jul;36(1):82-5.
doi: 10.1111/j.1365-2125.1993.tb05898.x.

The effects of indomethacin and naproxen on zidovudine pharmacokinetics

Affiliations
Clinical Trial

The effects of indomethacin and naproxen on zidovudine pharmacokinetics

M Barry et al. Br J Clin Pharmacol. 1993 Jul.

Abstract

The effects of indomethacin and naproxen on zidovudine (ZDV) pharmacokinetics were studied in six patients with the acquired immunodeficiency syndrome (AIDS), AIDS related complex (ARC) or asymptomatic HIV disease using a placebo-controlled crossover design. Indomethacin 25 mg twice daily or naproxen 250 mg twice daily did not alter ZDV pharmacokinetics compared with placebo. The mean AUC value for the glucuronidated metabolite, GZDV, was reduced from 26.6 +/- 11.7 mumol l-1 h in the presence of placebo to 20.9 +/- 8.3 mumol l-1 h (95% C.I. of the difference 1.39-9.98; P < 0.05) following treatment with naproxen 250 mg twice daily for 3 days. The small decrease in plasma GZDV in the naproxen phase reflects an increase in clearance of ZDV to other metabolites and/or a decrease in the formation clearance to GZDV and/or an increase in the clearance of GZDV. A decrease in formation clearance to GZDV would be consistent with the results of in vitro studies reported previously. No significant increase in ZDV concentration in the presence of naproxen may reflect a lower sensitivity of parent drug measurements to selective inhibition of parallel pathways of metabolism. The clinical significance of these findings is unknown but toxicity may be increased if a decreased formation of GZDV is accompanied by shunting of metabolism to 3'-amino-3'-deoxythymidine which is alleged to be cytotoxic.

PubMed Disclaimer

References

    1. Br J Surg. 1973 Aug;60(8):646-9 - PubMed
    1. J Clin Invest. 1985 Aug;76(2):875-7 - PubMed
    1. Br J Clin Pharmacol. 1987 Feb;23(2):189-93 - PubMed
    1. Clin Pharmacol Ther. 1987 Apr;41(4):407-12 - PubMed
    1. N Engl J Med. 1987 Jul 23;317(4):192-7 - PubMed

Publication types