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Clinical Trial
. 1988 Mar;157(3):502-7.
doi: 10.1093/infdis/157.3.502.

Vancomycin and the red-man syndrome: pharmacodynamics of histamine release

Affiliations
Clinical Trial

Vancomycin and the red-man syndrome: pharmacodynamics of histamine release

R E Polk et al. J Infect Dis. 1988 Mar.

Abstract

Two regimens for infusing vancomycin over 1 h (500 mg every 6 h for five doses or 100 mg every 12 h for three doses) were used in 11 volunteers. Subjects received both regimens one week apart; the regimen used first for each subject was randomized. Nine receiving the 1000-mg dose experienced the "red-man (neck)" syndrome; none had the reaction while receiving the 500-mg dose (P = .002). Plasma histamine concentration, measured every 10 min during the first infusion of each regimen, increased in most subjects given 1000-mg doses; there was only a slight change in histamine levels after 500-mg doses. There was a significant relation between histamine release and reaction severity; frequency and severity of the reaction declined with subsequent doses. We conclude that the red-man syndrome occurs frequently in normal adults who receive 1000 mg of vancomycin over 1 h, that vancomycin causes an infusion rate-dependent increase in plasma histamine concentration, and that the increase in plasma histamine concentration is correlated with the severity of the reaction.

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  • Red man syndrome.
    Sivagnanam S, Deleu D. Sivagnanam S, et al. Crit Care. 2003 Apr;7(2):119-20. doi: 10.1186/cc1871. Epub 2002 Dec 23. Crit Care. 2003. PMID: 12720556 Free PMC article.

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