Literature DB >> 1623916

Dose proportionality study of loperamide following oral administration of loperamide oxide.

F Kamali1, L Adriaens, M L Huang, R Woestenborghs, M Emanuel, M D Rawlins.   

Abstract

The pharmacokinetics of loperamide, after oral administration of increasing doses (1 to 16 mg) of loperamide oxide, has been investigated in 10 healthy male volunteers, using a randomised cross-over design. Comparison of the maximum plasma loperamide concentration and AUC demonstrated that the bioavailability of loperamide was proportional to the dose of loperamide oxide administered.

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Year:  1992        PMID: 1623916     DOI: 10.1007/bf00265940

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  1 in total

1.  P-glycoprotein-based loperamide-cyclosporine drug interaction at the rat blood-brain barrier: prediction from in vitro studies and extrapolation to humans.

Authors:  Peng Hsiao; Jashvant D Unadkat
Journal:  Mol Pharm       Date:  2012-02-17       Impact factor: 5.364

  1 in total

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