Clinical Equivalence between Generic Versus Branded Antibiotics: Systematic Review and Meta-Analysis

Regulatory authorities authorize the clinical use of generic drugs (GD) based on bioequivalence studies, which consist of the evaluation of pharmacokinetics after a single dose in vitro or in healthy individuals. There are few data on clinical equivalence between generic and branded antibiotics. Our...

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Detalles Bibliográficos
Autores principales: Cotia, André, Oliveira Junior, Haliton Alves, Matuoka, Jessica Y., Boszczowski, Ícaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215091/
https://www.ncbi.nlm.nih.gov/pubmed/37237838
http://dx.doi.org/10.3390/antibiotics12050935

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215091/
https://www.ncbi.nlm.nih.gov/pubmed/37237838
http://dx.doi.org/10.3390/antibiotics12050935

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