Adequate design of pharmacokinetic-pharmacodynamic studies will help optimize tuberculosis treatment for the future
- PMID: 25762792
- PMCID: PMC4356826
- DOI: 10.1128/AAC.05173-14
Adequate design of pharmacokinetic-pharmacodynamic studies will help optimize tuberculosis treatment for the future
Comment in
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Reply to "adequate design of pharmacokinetic-pharmacodynamic studies will help optimize tuberculosis treatment for the future".Antimicrob Agents Chemother. 2015 Apr;59(4):2475. doi: 10.1128/AAC.05182-14. Antimicrob Agents Chemother. 2015. PMID: 25762793 Free PMC article. No abstract available.
Comment on
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Effects of dosage, comorbidities, and food on isoniazid pharmacokinetics in Peruvian tuberculosis patients.Antimicrob Agents Chemother. 2014 Dec;58(12):7164-70. doi: 10.1128/AAC.03258-14. Epub 2014 Sep 15. Antimicrob Agents Chemother. 2014. PMID: 25224007 Free PMC article.
References
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- Magis-Escurra C, Later-Nijland HM, Alffenaar JW, Broeders J, Burger DM, van Crevel R, Boeree MJ, Donders AR, van Altena R, van der Werf TS, Aarnoutse RE. 2014. Population pharmacokinetics and limited sampling strategy for first-line tuberculosis drugs and moxifloxacin. Int J Antimicrob Agents 44:229–234. doi:10.1016/j.ijantimicag.2014.04.019. - DOI - PubMed
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