Editorial: pharmacoepidemiology and pharmacovigilance post-marketing drug safety studies.
| dc.creator | Zakir Khan | |
| dc.creator | Yusuf Karatas | |
| dc.creator | Ahmet Akici | |
| dc.creator | Maria Auxiliadora Parreiras Martins | |
| dc.creator | Nafees Ahmad | |
| dc.date.accessioned | 2026-03-04T14:34:49Z | |
| dc.date.issued | 2024-08-20 | |
| dc.identifier.doi | 10.3389/fphar.2024.1473052 | |
| dc.identifier.issn | 1663-9812 | |
| dc.identifier.uri | https://hdl.handle.net/1843/1918 | |
| dc.language | eng | |
| dc.publisher | Universidade Federal de Minas Gerais | |
| dc.relation.ispartof | Frontiers in pharmacology | |
| dc.rights | Acesso aberto | |
| dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Brazil | en |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/br/ | |
| dc.subject | Farmacovigilância | |
| dc.subject | Medicamentos | |
| dc.subject | Segurança do Paciente | |
| dc.subject | Evento Adverso | |
| dc.subject.other | Pharmacovigilance | |
| dc.subject.other | Drug | |
| dc.subject.other | Patient safety | |
| dc.subject.other | Real world data (RWD) | |
| dc.subject.other | Adverse events | |
| dc.title | Editorial: pharmacoepidemiology and pharmacovigilance post-marketing drug safety studies. | |
| dc.type | Artigo de periódico | |
| local.citation.epage | 3 | |
| local.citation.issue | 1473052 | |
| local.citation.spage | 1 | |
| local.citation.volume | 15 | |
| local.description.resumo | This article highlights the complementary roles of pharmacoepidemiology and pharmacovigilance in evaluating drug utilization, effectiveness, and safety in real-world settings. Drawing on 16 studies that used large pharmacovigilance databases and real-world data sources, the Research Topic explores adverse drug reactions, post-marketing safety surveillance, and signal detection across various medications and therapeutic areas. The findings emphasize the importance of continuous monitoring, integration of multiple data sources, and proactive safety assessment to ensure a favorable benefit–risk profile of marketed drugs. Overall, the collection reinforces the critical role of real-world evidence in supporting regulatory decisions and promoting rational drug use. | |
| local.publisher.country | Brasil | |
| local.publisher.department | FAR - DEPARTAMENTO DE PRODUTOS FARMACÊUTICOS | |
| local.publisher.initials | UFMG | |
| local.subject.cnpq | CIENCIAS DA SAUDE | |
| local.url.externa | http://www.frontiersin.org/pharmacology/archive |
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