Publication: Body weight cutoff for daily dosage of efavirenz and 60-week efficacy of efavirenz-based regimen in human immunodeficiency virus and tuberculosis coinfected patients receiving rifampin
dc.contributor.author | Weerawat Manosuthi | en_US |
dc.contributor.author | Somnuek Sungkanuparph | en_US |
dc.contributor.author | Preecha Tantanathip | en_US |
dc.contributor.author | Wiroj Mankatitham | en_US |
dc.contributor.author | Aroon Lueangniyomkul | en_US |
dc.contributor.author | Supeda Thongyen | en_US |
dc.contributor.author | Boonchuay Eampokarap | en_US |
dc.contributor.author | Sumonmal Uttayamakul | en_US |
dc.contributor.author | Pawita Suwanvattana | en_US |
dc.contributor.author | Samroui Kaewsaard | en_US |
dc.contributor.author | Kiat Ruxrungtham | en_US |
dc.contributor.other | Thailand Ministry of Public Health | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | The HIV Netherlands Australia Thailand Research Collaboration | en_US |
dc.contributor.other | Bamrasnaradura Infectious Diseases Institute | en_US |
dc.date.accessioned | 2018-09-13T06:53:54Z | |
dc.date.available | 2018-09-13T06:53:54Z | |
dc.date.issued | 2009-10-01 | en_US |
dc.description.abstract | Seventy-one human immunodeficiency virus-infected patients with tuberculosis who were receiving a rifampin (rifampicin)-containing regimen were initiated on treatment with efavirenz at 600 mg/day plus stavudine-lamivudine. Fasting efavirenz concentrations at 12 h after dosing (C12) were monitored. The mean ± standard deviation efavirenz C12 at weeks 6 and 12 and after rifampin discontinuation were 4.5 ± 4.3, 3.8 ± 3.5, and 3.5 ± 2.7 mg/liter, respectively. High body weight was associated with a low efavirenz C12 at weeks 6 and 12 (P = 0.003, r = -0.255). The efavirenz C12 regression prediction line at 1 mg/liter intercepted a mean body weight of 57.5 kg. Copyright © 2009, American Society for Microbiology. All Rights Reserved. | en_US |
dc.identifier.citation | Antimicrobial Agents and Chemotherapy. Vol.53, No.10 (2009), 4545-4548 | en_US |
dc.identifier.doi | 10.1128/AAC.00492-09 | en_US |
dc.identifier.issn | 10986596 | en_US |
dc.identifier.issn | 00664804 | en_US |
dc.identifier.other | 2-s2.0-70349313476 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/27919 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349313476&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Body weight cutoff for daily dosage of efavirenz and 60-week efficacy of efavirenz-based regimen in human immunodeficiency virus and tuberculosis coinfected patients receiving rifampin | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349313476&origin=inward | en_US |