Disposition of intravenous and oral cyclosporine after administration with grapefruit juice*
β Scribed by Ducharme, Murray P.; Warbasse, Lawrence H.; Edwards, David J.
- Publisher
- Nature Publishing Group
- Year
- 1995
- Tongue
- English
- Weight
- 636 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0009-9236
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The pharmacokinetics of ftorafur (FT), an antineoplastic agent, has been studied in seven cancer patients by determining concentrations of the unchanged compound in serum after single IV and PO doses of 2 g FT. Serum drug concentrations were determined by a new quantitative thin-layer chromatographi
Two studies of dl-2-(3-phenoxyphenyl)propionic acid or fenoprofen are described. In these studies, the pharmacokinetic parameters of fenoprofen administered orally and intravenously were compared first and then urine and plasma kinetics were compared. The results indicate that: (u) fenoprofen is rap
The objective of the study was to investigate the systemic disposition of 14C-SK&F L-190144 after single intravenous (10 mg kg-I) and oral (200 mg kg-I) doses to rats and after single intravenous and ocular doses (0.33 mg kg-I) to monkeys. After the intravenous dose, the blood concentration-time pr