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Adverse event reporting tools and regulatory measures in India through outcome of pharmacovigilance programme of India

The primary care medical practitioners as well as common public must be made aware of the importance and benefits of reporting adverse drug reactions (ADRs). The reporting of ADRs through periodic safety update reports is a regulatory requirement in many countries including India, however, the impor...

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Detalles Bibliográficos
Autores principales: Prakash, Jai, Sachdeva, Raghav, Shrivastava, Tarani Prakash, Jayachandran, C. V., Sahu, Aseem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265409/
https://www.ncbi.nlm.nih.gov/pubmed/34100398
http://dx.doi.org/10.4103/ijp.ijp_901_20

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