The single and multiple dose pharmacokinetics of nifedipine were examined in five patients taking the drug as part of protocol 81- H-159. This study demonstrates for the first time that nifedipine accumulates, in the body when administrated to typical patients in a conventional oral dosage schedule. We have shown that the serum nifedipine concentrations at steady state were, on average, 30% higher than the concentrations measured after the first dose. Because of accumulation, single dose pharmacokinetic and pharmacodynamic characteristics of nifedipine will, most likely, be dissimilar. It may be useful to utilize single dose kinetic parameter values to predict study state accumulation of nifedipine in future studies of nifedipine disposition and efficacy.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL005059-04
Application #
3939450
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code