2. Clinical Pharmacokinetics: Application to Bed Side through Extensive Understanding of the Whole Pharmacokinetic Processes in Human Body; Focus on the Renal Drug Excretion
Author:
Affiliation:
1. Department of Clinical Pharmacokinetics, Graduate School of Pharmaceutical Sciences, Kyushu University
Publisher
Japanese Society of Clinical Pharmacology and Therapeutics
Subject
Pharmacology (medical),Pharmacology
Link
https://www.jstage.jst.go.jp/article/jscpt/47/2/47_56/_pdf
Reference7 articles.
1. 1) Herrera J, Vukovich RA, Griffith DL. Elimination of nadolol by patients with renal impairment. Br J Clin Pharmacol. 1979; 7 Suppl 2: 227S-231S.
2. 2) Nakata J, Ohsawa I, Onda K, Tanimoto M, Kusaba G, Takeda Y, et al. Risk of overestimation of kidney function using GFR-estimating equations in patients with low inulin clearance. J Clin Lab Anal. 2012; 26(4): 248-53. doi: 10.1002/jcla.21513.
3. 3) Andreev E, Koopman M, Arisz L. A rise in plasma creatinine that is not a sign of renal failure: which drugs can be responsible? J Intern Med. 1999; 246(3): 247-52.
4. 4) Lepist EI, Ray AS. Renal drug-drug interactions: what we have learned and where we are going. Expert Opin Drug Metab Toxicol. 2012; 8(4): 433-48. doi: 10.1517/17425255.2012.667401.
5. 5) Liu R, Tang AM, Tan YL, Limenta LM, Lee EJ. Effects of sodium bicarbonate and ammonium chloride pre-treatments on PEPT2 (SLC15A2) mediated renal clearance of cephalexin in healthy subjects. Drug Metab Pharmacokinet. 2011; 26(1): 87-93.
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