Publication:
Pharmacokinetics of nevirapine in HIV and tuberculosis-coinfected children receiving antiretroviral fixed-dose combination tablets while receiving rifampicin-containing tuberculosis treatment and after rifampicin discontinuation

dc.contributor.authorWasana Prasitsuebsaien_US
dc.contributor.authorTim R. Cresseyen_US
dc.contributor.authorEdmund Capparellien_US
dc.contributor.authorNirun Vanpraparen_US
dc.contributor.authorKeswadee Lapphraen_US
dc.contributor.authorKulkanya Chokephaibulkiten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChiang Mai Universityen_US
dc.contributor.otherHarvard School of Public Healthen_US
dc.contributor.otherUniversity of California, San Diegoen_US
dc.date.accessioned2018-06-11T05:13:49Z
dc.date.available2018-06-11T05:13:49Z
dc.date.issued2012-04-01en_US
dc.description.abstractWe assessed the pharmacokinetics of nevirapine in HIV and tuberculosis-coinfected children while they were receiving nevirapine-containing fixed-dose combination tablets with rifampicin-based tuberculosis treatment and after discontinuation. The median age (range) was 9.7 (4.4-11.7) years. The nevirapine area under the concentration versus time curve from 0 to12 hours and trough concentration with rifampicin were 85.3 (40.5-170.7) mg.h/mL and 6.4 (3.00-13.27) mg/mL, respectively, providing adequate exposure. © 2012 by Lippincott Williams & Wilkins.en_US
dc.identifier.citationPediatric Infectious Disease Journal. Vol.31, No.4 (2012), 389-391en_US
dc.identifier.doi10.1097/INF.0b013e3182401c41en_US
dc.identifier.issn15320987en_US
dc.identifier.issn08913668en_US
dc.identifier.other2-s2.0-84858800794en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/14881
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84858800794&origin=inwarden_US
dc.subjectMedicineen_US
dc.titlePharmacokinetics of nevirapine in HIV and tuberculosis-coinfected children receiving antiretroviral fixed-dose combination tablets while receiving rifampicin-containing tuberculosis treatment and after rifampicin discontinuationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84858800794&origin=inwarden_US

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