Literature DB >> 8453848

A potentially hazardous interaction between erythromycin and midazolam.

K T Olkkola1, K Aranko, H Luurila, A Hiller, L Saarnivaara, J J Himberg, P J Neuvonen.   

Abstract

Interaction between erythromycin and midazolam was investigated in two double-blind, randomized, crossover studies. In the first study, 12 healthy volunteers were given 500 mg erythromycin three times a day or placebo for 1 week. On the sixth day, the subjects ingested 15 mg midazolam. In the second study, midazolam (0.05 mg/kg) was given intravenously to six of the same subjects, after similar pretreatments. Plasma samples were collected, and psychomotor performance was measured. Erythromycin increased the area under the midazolam concentration-time curve after oral intake more than four times (p < 0.001) and reduced clearance of intravenously administered midazolam by 54% (p < 0.05). In psychomotor tests (e.g., saccadic eye movements), the interaction between erythromycin and orally administered midazolam was statistically significant (p < 0.05) from 15 minutes to 6 hours. Metabolism of both erythromycin and midazolam by the same cytochrome P450IIIA isozyme may explain the observed pharmacokinetic interaction. Prescription of midazolam for patients receiving erythromycin should be avoided or the dose of midazolam should be reduced by 50% to 75%.

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Year:  1993        PMID: 8453848     DOI: 10.1038/clpt.1993.25

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  63 in total

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7.  In vivo information-guided prediction approach for assessing the risks of drug-drug interactions associated with circulating inhibitory metabolites.

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8.  Should Midazolam Drug-Drug Interactions be of Concern to Palliative Care Physicians?

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9.  Effect of route of administration of fluconazole on the interaction between fluconazole and midazolam.

Authors:  J Ahonen; K T Olkkola; P J Neuvonen
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10.  CYP3A4 and CYP2A6 activities marked by the metabolism of lignocaine and coumarin in patients with liver and kidney diseases and epileptic patients.

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Journal:  Br J Clin Pharmacol       Date:  1995-01       Impact factor: 4.335

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