𝔖 Bobbio Scriptorium
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Disposition of valproic acid in man

✍ Scribed by R. Gugler; A. Schell; M. Eichelbaum; W. Fröscher; H. -U. Schulz


Publisher
Springer
Year
1977
Tongue
English
Weight
749 KB
Volume
12
Category
Article
ISSN
0031-6970

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The disposition of the b-blocking drug talinolol is controlled by P-glycoprotein in man. Because talinolol is marketed as a racemate, we reevaluated the serum-concentration time pro®les of talinolol of a previously published study with single intravenous (30 mg) and repeated oral talinolol (100 mg f