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.
引用
收藏
页码:693 / 694
页数:2
相关论文
共 4 条
[1]
HEYKANTS J, 1991, 3RD INT ISSX M DRUG
[2]
LAVRIJSEN K, 1984, ARCH INT PHARMACOD T, V270, P174