Generic vancomycin products fail in vivo despite being pharmaceutical equivalents of the innovator

ABSTRACT: Generic versions of intravenous antibiotics are not required to demonstrate therapeutic equivalence with the innovator because therapeutic equivalence is assumed from pharmaceutical equivalence. To test such assump tions, we studied three generic versions of vancomycin in simultaneous expe...

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Autores:
Agudelo García, Olga María
Salazar Giraldo, Beatriz
Rodríguez Jaramillo, Carlos Andrés
Zuluaga Salazar, Andrés Felipe
Vesga Meneses, Omar
Tipo de recurso:
Article of investigation
Fecha de publicación:
2010
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/43569
Acceso en línea:
https://hdl.handle.net/10495/43569
Palabra clave:
Medicamentos Genéricos
Drugs, Generic
Pruebas de Sensibilidad Microbiana
Microbial Sensitivity Tests
Neutropenia
Neutropenia
Infecciones Estafilocócicas
Staphylococcal Infections
Equivalencia Terapéutica
Therapeutic Equivalency
Insuficiencia del Tratamiento
Treatment Failure
Vancomicina
Vancomycin
Antibacterianos
Anti-Bacterial Agents
https://id.nlm.nih.gov/mesh/D016568
https://id.nlm.nih.gov/mesh/D008826
https://id.nlm.nih.gov/mesh/D009503
https://id.nlm.nih.gov/mesh/D013203
https://id.nlm.nih.gov/mesh/D013810
https://id.nlm.nih.gov/mesh/D017211
https://id.nlm.nih.gov/mesh/D014640
https://id.nlm.nih.gov/mesh/D000900
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Generic versions of intravenous antibiotics are not required to demonstrate therapeutic equivalence with the innovator because therapeutic equivalence is assumed from pharmaceutical equivalence. To test such assump tions, we studied three generic versions of vancomycin in simultaneous experiments with the innovator and determined the concentration and potency of the active pharmaceutical ingredient by microbiological assay, single-dose pharmacokinetics in infected mice, antibacterial effect by broth microdilution and time-kill curves (TKC), and pharmacodynamics against two wild-type strains of Staphylococcus aureus by using the neutropenic mouse thigh infection model. The main outcome measure was the comparison of magnitudes and patterns of in vivo efficacy between generic products and the innovator. Except for one product exhibiting slightly greater concentration, vancomycin generics were undistinguishable from the innovator based on concentration and potency, protein binding, in vitro antibacterial effect determined by minimal inhibitory or bactericidal concen trations and TKC, and serum pharmacokinetics. Despite such similarities, all generic products failed in vivo to kill S. aureus, while the innovator displayed the expected bactericidal efficacy: maximum antibacterial effect (Emax) (95% confidence interval [CI]) was 2.04 (1.89 to 2.19), 2.59 (2.21 to 2.98), and 3.48 (2.92 to 4.04) versus 5.65 (5.52 to 5.78) log10 CFU/g for three generics and the innovator product, respectively (P < 0.0001, any comparison). Nonlinear regression analysis suggests that generic versions of vancomycin contain inhibitory and stimulatory principles within their formulations that cause agonistic-antagonistic actions responsible for in vivo failure. In conclusion, pharmaceutical equivalence does not imply therapeutic equivalence for vancomycin.