๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Bioavailability of medroxalol in man

โœ Scribed by Frederick J. Keeley; Daniel L. Weiner; Richard A. Okerholm


Publisher
John Wiley and Sons
Year
1983
Tongue
English
Weight
226 KB
Volume
4
Category
Article
ISSN
0142-2782

No coin nor oath required. For personal study only.

โœฆ Synopsis


Ten healthy male volunteers received single oral doses of l00mg of medroxalol administered as a solution, a preliminary tablet formulation and a single dose of lOOmg administered intravenously in a randomized three-way crossover study. Mean terminal half-lives of 12.4, 13.4, and 11.3 h were observed for the intravenous, solution and tablet formulation, respectively.

Mean urinary recovery of parent drug at 48 h was 8.9 per cent, 3.9 per cent, and 3.2 per cent. Absolute bioavailability estimated from plasma AUC was 54 per cent for the solution and 38 per cent for the tablet, and the relative bioavailability from the tablet was 71 per cent.


๐Ÿ“œ SIMILAR VOLUMES


Bioavailability of terfenadine in man
โœ R. A. Okerholm; D. L. Weiner; R. H. Hook; B. J. Walker; G. A. Leeson; S. A. Bied ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 276 KB

## Abstract Fourteen normal male subjects were given either 60 mg or 180mg of terfenadine suspension in a randomized twoโ€way crossover study. Peak plasma concentrations of 1.544 ยฑ 0.726 (mean ยฑ S.D.) ng ml^โˆ’1^ were obtained in 0.786 ยฑ 0.426 h following the 60 mg dose and displayed an AUC of 11.864

Systemic bioavailability of acebutolol i
โœ A. Roux; B. Flouvat; Y. Fouache; J. P. Bourdarias ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 219 KB ๐Ÿ‘ 1 views
Bioavailability of seven furosemide tabl
โœ Arthur B. Straughn; George C. Wood; Gursharan Raghow; Marvin C. Meyer ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 385 KB ๐Ÿ‘ 2 views

A seven-way crossover study was conducted in 14 healthy male volunteers to evaluate the relative bioavailability of seven different marketed 40 mg furosemide tablets. Each dose was administered as a single tablet after an overnight fast. and blood samples were obtained for 16 hours. Plasma was assay

Estimation of the systemic bioavailabili
โœ Ragab El-Rashidy ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 263 KB ๐Ÿ‘ 1 views

## Introduction Recently, the pharmacokinetics of timolol, a padrenergic blocking agent and a propranolol analog, were reported for normal volunteers and uremic patients after oral administration. Clinically, timolol is more potent when compared to propranolol and alprenolol as an antihypertensive

Dissolution rate-limited absorption and
โœ Kerstin Strandgรฅrden; Peter Hรถglund; ร–rjan Nordle; Jiri Polacek; Hans Wรคnnman; P ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 144 KB ๐Ÿ‘ 1 views

In order to investigate the bioavailability and the rate-limiting step of the absorption of roquinimex, an oral solution and a tablet formulation (Linomide ยฎ ) were given to healthy volunteers. The study was conducted as a randomized three-period crossover study in seven male and seven female health

Bioavailability in man of atenolol and c
โœ James McAinsh; William Bastain; Jean Young; John D. Harry ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 428 KB ๐Ÿ‘ 1 views

## Abstract In this comparative bioavailability study in 12 healthy volunteers the blood level profiles and urinary recoveries of both atenolol and chlorthalidone were studied following the administration of the drug as a fixed combination (โ€˜Tenoreticโ€™), as a free combination, and individually, at