Low Bioavailability of Oral Tacrolimus Suspension in Pediatric Kidney Transplant Patients
Author:
Funder
Nierstichting
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology
Link
https://link.springer.com/content/pdf/10.1007/s40262-020-00908-9.pdf
Reference8 articles.
1. Bastiaans DE, Cressey TR, Vromans H, Burger DM. The role of formulation on the pharmacokinetics of antiretroviral drugs. Expert Opin Drug Metab Toxicol. 2014;10(7):1019–37. https://doi.org/10.1517/17425255.2014.925879.
2. Labberton L, Herder RE, Bolhuis MS, Schellekens RCA, Uges DRA. Formulation of a tacrolimus suspension with an extended expiry date in a hospital pharmacy. Eur J Hosp Pharmacy. 2011;17:36–40.
3. Reding R, Sokal E, Paul K, Janssen M, Evrard V, Wilmotte L, et al. Efficacy and pharmacokinetics of tacrolimus oral suspension in pediatric liver transplant recipients. Pediatr Transplant. 2002;6(2):124–6.
4. Bekersky I, Dressler D, Mekki QA. Effect of low- and high-fat meals on tacrolimus absorption following 5 mg single oral doses to healthy human subjects. J Clin Pharmacol. 2001;41(2):176–82. https://doi.org/10.1177/00912700122009999.
5. Undre N, Baccarani U, Britz R, Popescu I. Pharmacokinetic profile of prolonged-release tacrolimus when administered via nasogastric tube in de novo liver transplantation: a sub-study of the DIAMOND trial. Ann Transplant. 2019;24:268–72. https://doi.org/10.12659/AOT.909693.
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1. Distribution evaluation of tacrolimus in the ascitic fluid of liver transplant recipients with liver cirrhosis by a sensitive ultra‐performance liquid chromatography‐tandem mass spectrometry method;Journal of Separation Science;2021-11-05
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