A Population Pharmacokinetic Model to Predict the Individual Starting Dose of Tacrolimus Following Pediatric Renal Transplantation-Reference-Cited by-同舟云学术

A Population Pharmacokinetic Model to Predict the Individual Starting Dose of Tacrolimus Following Pediatric Renal Transplantation

Published:2017-07-05 Issue:4 Volume:57 Page:475-489
ISSN:0312-5963
Container-title:Clinical Pharmacokinetics
language:en
Short-container-title:Clin Pharmacokinet

Author:

Andrews Louise M.^ORCID,Hesselink Dennis A.,van Gelder Teun,Koch Birgit C. P.,Cornelissen Elisabeth A. M.,Brüggemann Roger J. M.,van Schaik Ron H. N.,de Wildt Saskia N.,Cransberg Karlien,de Winter Brenda C. M.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/article/10.1007/s40262-017-0567-8/fulltext.html

Reference54 articles.

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2. Meier-Kriesche HU, Li S, Gruessner RW, Fung JJ, Bustami RT, Barr ML, et al. Immunosuppression: evolution in practice and trends, 1994–2004. Am J Transpl. 2006;6(5 Pt 2):1111–31.

3. Burckart GJ, Liu XI. Pharmacogenetics in transplant patients: can it predict pharmacokinetics and pharmacodynamics? Ther Drug Monit. 2006;28(1):23–30.

4. Hesselink DA, van Schaik RH, van Agteren M, de Fijter JW, Hartmann A, Zeier M, et al. CYP3A5 genotype is not associated with a higher risk of acute rejection in tacrolimus-treated renal transplant recipients. Pharmacogenet Genom. 2008;18(4):339–48.

5. Naesens M, Kuypers DR, Sarwal M. Calcineurin inhibitor nephrotoxicity. Clin J Am Soc Nephrol. 2009;4(2):481–508.

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