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Key pharmacovigilance stakeholders' experiences of direct patient reporting of adverse drug reactions and their prospects of future development in the European Union.

Author
Abstract
:

In the European Union (EU), legislation allows patients to directly report adverse drug reactions (ADRs) to competent authorities. Five years after its implementation, patient reporting is not equal in all countries. This study aimed to explore key stakeholders' perceptions of patient reporting in four EU countries.

Year of Publication
:
2018
Journal
:
Public health
Volume
:
155
Number of Pages
:
119-128
Date Published
:
2018
ISSN Number
:
0033-3506
URL
:
http://linkinghub.elsevier.com/retrieve/pii/S0033-3506(17)30398-0
DOI
:
10.1016/j.puhe.2017.11.023
Short Title
:
Public Health
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