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Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

BACKGROUND: Voluntary reports on adverse events (AEs) submitted by consumers have been facilitated through the MedWatch program in the United States (US), but few studies have described the characteristics of voluntary reports. OBJECTIVE: The aim of this study was to reveal the characteristics of cu...

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Библиографические подробности
Опубликовано в: :Drugs Real World Outcomes
Главные авторы: Toki, Tadashi, Ono, Shunsuke
Формат: Artigo
Язык:Inglês
Опубликовано: Springer International Publishing 2018
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5984610/
https://ncbi.nlm.nih.gov/pubmed/29725886
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40801-018-0134-0
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