Pharmacokinetics and safety of the two oral cefaclor formulations in healthy chinese subjects in the fasting and postprandial states

We conducted a phase I bioequivalence trial in healthy Chinese subjects in the fasting and postprandial states. The goal of this trial was to compare the pharmacokinetics and safety of the test preparation Cefaclor granule (Disha Pharmaceutical Group Co., Ltd.) and the reference preparation Cefaclor...

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Detalles Bibliográficos
Autores principales: Qu, Xinyao, Deng, Qiaohuan, Li, Ying, Li, Peng, Liu, Guangwen, Wang, Yanli, Liu, Zhengzhi, Yu, Shuang, Cheng, Yang, Zhou, Yannan, Chen, Jiahui, Ren, Qing, Yu, Zishu, Su, Zhengjie, Zhao, Yicheng, Yang, Haimiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581244/
https://www.ncbi.nlm.nih.gov/pubmed/36278160
http://dx.doi.org/10.3389/fphar.2022.1012294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581244/
https://www.ncbi.nlm.nih.gov/pubmed/36278160
http://dx.doi.org/10.3389/fphar.2022.1012294

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