Severe Malaria, Pascalian Therapeutics, and the US Food and Drug Administration (FDA)-Reference-Cited by-同舟云学术

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Severe Malaria, Pascalian Therapeutics, and the US Food and Drug Administration (FDA)

Published:2022-01-01 Issue:2 Volume:75 Page:358-358
ISSN:1058-4838
Container-title:Clinical Infectious Diseases
language:en
Short-container-title:

Author:

White Nicholas J¹,Watson James A¹,Simpson Julie A²

Affiliation:

1. Mahidol Oxford Research Unit, Faculty of Tropical Medicine, Mahidol University , Bangkok Thailand

2. Biostatistics Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne , Parkville, Victoria , Australia

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Link

https://academic.oup.com/cid/advance-article-pdf/doi/10.1093/cid/ciac024/42556128/ciac024.pdf

Reference9 articles.

1. AQUAMAT group. Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial.;Dondorp;Lancet,2010

2. Population pharmacokinetics of intramuscular artesunate in African children with severe malaria: implications for a practical dosing regimen.;Hendriksen;Clin Pharmacol Ther,2013

3. Population pharmacokinetics of intravenous artesunate: a pooled analysis of individual data from patients with severe malaria.;Zaloumis;CPT Pharmacometrics Syst Pharmacol,2014

4. Effect of body weight and age on the pharmacokinetics of dihydroartemisinin: Food and Drug Administration basis for dose determination of artesunate for injection in pediatric patients with severe malaria.;Kitabi;Clin Infect Dis,2021

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