Please use this identifier to cite or link to this item: https://doi.org/10.1046/j.1365-2125.2002.01647.x
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dc.titleQuinidine does not affect the renal clearance of moxonidine
dc.contributor.authorWise, S.D.
dc.contributor.authorChan, C.
dc.contributor.authorSchaefer, H.G.
dc.contributor.authorHe, M.M.
dc.contributor.authorPouliquen, I.J.
dc.contributor.authorMitchell, M.I.
dc.date.accessioned2016-11-16T11:04:41Z
dc.date.available2016-11-16T11:04:41Z
dc.date.issued2002
dc.identifier.citationWise, S.D., Chan, C., Schaefer, H.G., He, M.M., Pouliquen, I.J., Mitchell, M.I. (2002). Quinidine does not affect the renal clearance of moxonidine. British Journal of Clinical Pharmacology 54 (3) : 251-254. ScholarBank@NUS Repository. https://doi.org/10.1046/j.1365-2125.2002.01647.x
dc.identifier.issn03065251
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/130324
dc.description.abstractAims: To test the hypothesis that the renal clearance of moxonidine decreases when dosed with quinidine. Methods: A randomized, two-period study was conducted with six healthy, male subjects orally dosed with either 0.2 mg moxonidine alone or 1 h after 400 mg quinidine sulphate. Pharmacokinetic parameters were calculated using a noncompartmental analysis method. Results: When coadministered, quinidine significantly increased moxonidine AUC and t1/2 by 11% and 15%, respectively, and decreased CL/F by 10% compared with the control dosing. CLR and Aeur were not significantly different. Clinically, both treatments were well tolerated. Conclusions: Quinidine does not affect the renal clearance of moxonidine. The decrease in apparent total clearance of moxonidine with quinidine coadministration was possibly due to metabolic inhibition, though not likely to be clinically significant.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1046/j.1365-2125.2002.01647.x
dc.sourceScopus
dc.subjectMoxonidine
dc.subjectPharmacokinetics
dc.subjectQuinidine
dc.subjectRenal
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1046/j.1365-2125.2002.01647.x
dc.description.sourcetitleBritish Journal of Clinical Pharmacology
dc.description.volume54
dc.description.issue3
dc.description.page251-254
dc.description.codenBCPHB
dc.identifier.isiut000178081300003
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