Werner Siegmund
Department of Clinical Pharmacology
Ernst Moritz Arndt University
Felix-Hausdorff-Str. 3
D-17487 Greifswald
Germany
Name/email consistency: high
- Clarithromycin is absorbed by an intestinal uptake mechanism that is sensitive to major inhibition by rifampicin: results of a short-term drug interaction study in foals. Peters, J., Eggers, K., Oswald, S., Block, W., Lütjohann, D., Lämmer, M., Venner, M., Siegmund, W. Drug Metab. Dispos. (2012)
- Oral absorption of clarithromycin is nearly abolished by chronic comedication of rifampicin in foals. Peters, J., Block, W., Oswald, S., Freyer, J., Grube, M., Kroemer, H.K., Lämmer, M., Lütjohann, D., Venner, M., Siegmund, W. Drug Metab. Dispos. (2011)
- Pharmacokinetics and pharmacodynamics of propiverine in children aged between 5 and 10 years with symptoms of overactive bladder. Siegmund, W., Sillén, U., Läckgren, G., Schnabel, F., Mürtz, G., Feustel, C. Clin. Pharmacokinet (2010)
- Effect of levothyroxine administration on intestinal P-glycoprotein expression: consequences for drug disposition. Siegmund, W., Altmannsberger, S., Paneitz, A., Hecker, U., Zschiesche, M., Franke, G., Meng, W., Warzok, R., Schroeder, E., Sperker, B., Terhaag, B., Cascorbi, I., Kroemer, H.K. Clin. Pharmacol. Ther. (2002)
- The effects of the human MDR1 genotype on the expression of duodenal P-glycoprotein and disposition of the probe drug talinolol. Siegmund, W., Ludwig, K., Giessmann, T., Dazert, P., Schroeder, E., Sperker, B., Warzok, R., Kroemer, H.K., Cascorbi, I. Clin. Pharmacol. Ther. (2002)