Titlebook: Cardiac Glycosides; Günter Bodem,Hans J. Dengler Conference proceedings 1978 Springer-Verlag Berlin Heidelberg 1978 Bypass.Herzglykosid.as

使閉塞

https://doi.org/10.1007/978-1-349-00412-6bjects maintained on the drug in standard oral tablet form. Only 21%–55% of the daily dose was excreted in the urine and feces as the chemically intact glycoside; the rest was biotransformed. Since the only acid-hydrolyzable derivative of digoxigenin that was recovered from urine and feces was digox

甜得發(fā)膩

尊嚴

Christoph Korbmacher,Colin J. Barnstable al., 1970; Lahrtz et al., 1969; Okita et al., 1953,1955; V?hringer and Rietbrock, 1974; Weissler et al., 1966) as well as from multiple dose studies (Jelliffe, 1967; Lukas, 1971,1973; Peters et al., 1975; Solomon et al., 1971; Storstein, 1974; Wirth et al., 1976) using different methods, can be cha

漂浮

終止

典型

L. Donald Partridge,Dieter Swandullade-effects of cardiac glycosides can be categorized into two generai classes, those of a neurologic nature including fatigue, loss of appetite, vomiting, color vision, central scotoma, states of confusion and delirium, and those of a cardiac nature, primarily those of alterations in cardiac rate and

linguistics

不透氣

Conflict

使虛弱

Gene Christner,Kin Y. Li,James Rovnyakaum et. al., 1971). On the other hand, only few studies are available about the absorption of digoxin under pathological conditions. Therefore, in the present study, three different studies were performed. In the first study, different pharmacokinetic parameters after oral administration of digoxin