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Eur J Clin Pharmacol ; 61(9): 621-5, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16133549

ABSTRACT

OBJECTIVE: To determine whether co-administration of rosuvastatin alters the pharmacodynamics of warfarin, thereby requiring additional monitoring of the anticoagulant effects of warfarin. METHODS: In this open-labeled, placebo-controlled, randomized, two-period, crossover trial with a washout period of 15 days, 12 healthy male volunteers were administered daily oral doses of 5 mg warfarin for 14 days. Either rosuvastatin 40 mg/day (treatment A) or placebo (treatment B) was concomitantly administered on days 8-14. The pharmacodynamic parameters prothrombin time (PT) and international normalized ratio (INR) were evaluated on all 14 days pre-dose during both study periods. On the 8th, 10th, 12th, and 14th days of each study period, PT and INR were also measured at 4 h post-dose of rosuvastatin or placebo. Bleeding time and clotting time were assessed on the 1st, 8th, and 14th days pre-dose. RESULTS: Data of 10 subjects have been analyzed. No significant effect of rosuvastatin was seen on the steady-state pharmacodynamics of warfarin during concomitant administration. CONCLUSION: Rosuvastatin did not significantly alter the anticoagulant effects of warfarin in this study.


Subject(s)
Anticoagulants/pharmacokinetics , Fluorobenzenes/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Pyrimidines/pharmacology , Sulfonamides/pharmacology , Warfarin/pharmacokinetics , Administration, Oral , Adult , Anticoagulants/administration & dosage , Blood Coagulation/drug effects , Cross-Over Studies , Drug Interactions , Drug Therapy, Combination , Humans , International Normalized Ratio , Male , Prothrombin Time , Rosuvastatin Calcium , Warfarin/administration & dosage
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