Zobrazeno 1 - 10
of 16
pro vyhledávání: '"S. L. Steelman"'
Publikováno v:
British Journal of Clinical Pharmacology. 4:31S-36S
1 In the fasting state, peak plasma levels of diflunisal were achieved within 2 hours. The drug was not metabolized and almost totally excreted in the urine as unchanged or conjugated drug. The terminal plasma half-life was approximately 8 hours. The
Autor:
T. B. Tjandramaga, P. J. Deschepper, C. Daurio, M. De Roo, Kenneth F. Tempero, L. Verhaest, S. L. Steelman
Publikováno v:
Clinical Pharmacology & Therapeutics. 23:669-676
Fecal blood loss was evaluated in normal subjects with 51Cr-labeled red cells. In a double-blind parallel study in 10 subjects, 250 mg diflunisal twice daily did not significantly increase blood loss in two consecutive treatment periods, while 750 mg
Publikováno v:
Journal of International Medical Research. 6:172-179
A single dose experiment was used to evaluate the analgesic effect of diflunisal, a new salicylic acid derivative. Three dose levels of diflunisal (125 mg, 250 mg, and 500 mg) were compared to one dose level of acetylsalicylic acid (ASA) (600 mg) and
Publikováno v:
Current medical research and opinion. 5(7)
Faecal blood loss was measured in normal male volunteers using 51Cr-labelled red cells. In a double-blind parallel study in 10 subjects, the effect of 250 mg diflunisal twice daily was compared with 750 mg aspirin 4-times daily. Drugs were taken duri
Publikováno v:
Endocrinology. 119(4)
Mouse fibroblast cell lines which secrete bovine (b) GH have been generated. This was accomplished by cotransforming mouse L cells (thymidine kinase-negative [TK-] and adenine phosphoribosyl transferase-negative [APRT-]) with DNA molecules encoding t
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 3(6)
5-(2'4'-Difluorophenyl) [carboxy-14C]salicyclic acid (MK-647) was quickly and completely absorbed in rats, dogs, and man. Peak levels of plasma radioactivity occurred in 1-2 hr after oral administration. The dose was 10 mg/kg in rats and dogs, and 50
Publikováno v:
Advances in experimental medicine and biology. 188
Based upon the clinical finding that a Merck somatostatin-14 (S-14) analog induced steatorrhea in man, we sought to develop animal models to study the effects of S-14 and a series of synthetic analogs on absorption. Rats were trained to eat a diet (p
Publikováno v:
Current medical research and opinion. 5(7)
SummaryStudies are reviewed on diflunisal, a new analgesic agent with an improved therapeutic index, compared with acetylsalicylic acid, in animals and humans. Pharmacokinetic data indicate that a twice-daily dosage regimen of diflunisal is adequate
Autor:
B M, DOBYNS, S L, STEELMAN
Publikováno v:
Endocrinology. 52(6)