Relación entre buenas prácticas de farmacovigilancia y el reporte de reacciones adversas en una cadena de boticas, Lima 2025.
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Universidad Privada de Huancayo Franklin Roosevelt
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La investigación tuvo como objetivo determinar la relación entre las buenas prácticas de farmacovigilancia y el reporte de reacciones adversas en una cadena de boticas de Lima, 2025. El estudio fue de enfoque inductivo, prospectivo, no experimental, transversal y de nivel correlacional. La muestra estuvo conformada por directores técnicos de 30 oficinas farmacéuticas. Los resultados muestran alto cumplimiento en Sistemas de Calidad (83,3%), Infraestructura (80,0%), Personal (83,3%), POES (76,7%) y Gestión de Sospechas (73,3%). Además, el 86,7% reporta adecuadamente las reacciones adversas. Se encontró relación significativa entre las buenas prácticas y el reporte (p < 0.05). Se concluye que existe relación entre la aplicación de buenas prácticas de farmacovigilancia y el adecuado reporte de reacciones adversas.
The objective of the research was to determine the relationship between good pharmacovigilance practices and the reporting of adverse reactions in a chain of pharmacies in Lima, 2025. The study was inductive, prospective, non-experimental, cross-sectional, and correlational in nature. The sample consisted of technical directors from 30 pharmaceutical offices. The results show high compliance in Quality Systems (83.3%), Infrastructure (80.0%), Personnel (83.3%), POES (76.7%), and Suspicion Management (73.3%). In addition, 86.7% adequately report adverse reactions. A significant relationship was found between good practices and reporting (p < 0.05). It is concluded that there is a relationship between the application of good pharmacovigilance practices and the adequate reporting of adverse reactions.
The objective of the research was to determine the relationship between good pharmacovigilance practices and the reporting of adverse reactions in a chain of pharmacies in Lima, 2025. The study was inductive, prospective, non-experimental, cross-sectional, and correlational in nature. The sample consisted of technical directors from 30 pharmaceutical offices. The results show high compliance in Quality Systems (83.3%), Infrastructure (80.0%), Personnel (83.3%), POES (76.7%), and Suspicion Management (73.3%). In addition, 86.7% adequately report adverse reactions. A significant relationship was found between good practices and reporting (p < 0.05). It is concluded that there is a relationship between the application of good pharmacovigilance practices and the adequate reporting of adverse reactions.
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