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PMID: 7053283 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, U.S. Gov't, P.H.S.

Stereoselective interaction of sulfinpyrazone with racemic warfarin and its separated enantiomorphs in man.

Circulation ·Vol. 65 ·No. 1 ·1982-01-00 ·Pages 202-7

O'Reilly RA

Abstract

Although serious hemorrhage during therapeutic coadministration of sulfinpyrazone and racemic warfarin occurs, no prospective studies have been done. In this study, single oral doses of racemic warfarin, 1.5 mg/kg, were administered to six normal subjects with and without oral sulfinpyrazone, 400 mg daily. Both the hypoprothrombinemia (p less than 0.001) and the plasma warfarin concentrations (p less than 0.05) were significantly augmented. To determine if this interaction was stereoselective, the experiments were repeated in the same subjects with R-and S-warfarin enantiomorphs. S-warfarin with sulfinpyrazone caused a highly significant augmentation of both the hypoprothrombinemia (p less than 0.001) and the plasma warfarin concentrations (p less than 0.001). R-warfarin with sulfinpyrazone did not significantly change the hypoprothrombinemia but significantly (p less than 0.05) reduced warfarin concentrations. Thus, sulfinpyrazone augmented the hypoprothrombinemia of racemic warfarin stereoselectively by reduced metabolic clearance of S-warfarin. Sulfinpyrazone and racemic warfarin are most dangerous when either drug is added to a stabilized regimen of the other drug.

MeSH Terms
Adult Drug Synergism Half-Life Humans Hypoprothrombinemias/blood,chemically induced Kinetics Male Prothrombin/metabolism Stereoisomerism Sulfinpyrazone/adverse effects Warfarin/adverse effects,blood
Chemicals
Warfarin Prothrombin Sulfinpyrazone
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
O'Reilly R A
Article Info
Journal
Circulation
Abbr.
Circulation
ISSN
0009-7322
Published
1982-01-00
Pages
202-7
Language
English
Region
United States
NLM ID
0147763
Subset
IM
Grants
NIGMS NIH HHS · GMS 22860-05 · United States
NHLBI NIH HHS · HL 8058-17 · United States
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