Zobrazeno 1 - 10
of 49
pro vyhledávání: '"J J, Ferry"'
Autor:
Sue Leurgans, Katie Kompoliti, L. C. Yones, M. T. Leibowitz, E. Tan, John N. Caviness, Rema Raman, Charles H. Adler, Paul M. Carvey, J. J. Ferry, Lucy M. Blasucci, J. H. Pincus, Christopher G. Goetz, W. M. Chase
Publikováno v:
Neurology. 58:1418-1422
The authors studied the pharmacokinetics of levodopa (LD) with and without pramipexole (PPX) in men and postmenopausal women with PD. Patients on stable dose of carbidopa/LD were randomized to receive escalating doses of placebo or PPX over 7 weeks.
Publikováno v:
European Journal of Clinical Pharmacology. 45:437-443
We have studied the pharmacokinetics and haemodynamic effects of nicorandil after a 12-h infusion. Nicorandil is a mixed vasodilator combining the actions of a nitrate and a potassium channel opener. Nicorandil was infused for 12 h in 21 healthy volu
Publikováno v:
European Journal of Clinical Pharmacology. 44:27-33
We have studied the effects of intravenous nicorandil, a mixed arterial and venous vasodilator, in 48 healthy volunteers. Nicorandil (20, 28, 39, 54, 74, 103, 144, or 200 μg·kg−1) or placebo were given over 5 min to subjects supine (16 subjects,
Publikováno v:
Biopharmaceuticsdrug disposition. 19(8)
To determine the effect of reduced hepatic function on the pharmacokinetics of minoxidil. The pharmacokinetics of antipyrine, lorazepam, and indocyanine green were included as indicators of hepatic function.Eight mild cirrhotics and eight healthy sub
Publikováno v:
The Journal of Clinical Pharmacology. 28:81-87
A randomized, four-way cross-over study was conducted in eight healthy male volunteers to determine the relative and absolute bioavailability of prednisone (PN) and prednisolone (PL). PN and PL were administered as single, oral 10-mg tablet doses and
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 12(4)
Publikováno v:
Journal of clinical pharmacology. 28(1)
The potential effect of cimetidine on the pharmacokinetic profiles of quinapril and its active metabolite CI-928 was evaluated in eight healthy volunteers. Each subject received a single 40-mg quinapril dose on days 1 and 12 and cimetidine 300 mg fou
Publikováno v:
Journal of chromatography. 421(1)
Publikováno v:
Journal of clinical pharmacology. 27(5)
A randomized two-way crossover study was conducted in 12 healthy volunteers to assess the effect of food on the pharmacokinetics of quinapril (CI-906) and its active metabolite, CI-928, after quinapril dosing. Forty-milligram oral quinapril doses wer
Autor:
J J, Ferry, I E, Redlener
Publikováno v:
Pediatrics. 81(5)