Patient Reporting of Adverse Drug Reactions: An International Survey of National Competent Authorities' Views and Needs.

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Abstract

Patient reporting of adverse drug reactions (ADRs) to spontaneous reporting systems can make a valuable contribution to pharmacovigilance. However, the implementation and promotion of patient reporting systems (PRSs) differ worldwide.

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Journal

Journal ID (iso-abbrev): Drug Saf

Title: Drug safety

Publisher: Springer Nature

ISSN (Electronic): 1179-1942

ISSN (Print): 0114-5916

Publication date (Electronic): Nov 2016

Volume: 39

Issue: 11

Affiliations

[1 ] Department of Pharmacology, Faculty of Pharmacy, University of Seville, C/Profesor García-González 2, 41012, Seville, Spain. cristiano.r.matos@gmail.com.

[2 ] Netherlands Pharmacovigilance Centre Lareb, World Health Organization Collaborating Centre for Pharmacovigilance in Education and Patient Reporting, Goudsbloemvallei 7, 5237 MH, 's-Hertogenbosch, The Netherlands.

Article

Publisher Item ID: 10.1007/s40264-016-0453-6

DOI: 10.1007/s40264-016-0453-6

PubMed ID: 27581398

SO-VID: 6dc62227-1936-4b8a-b39c-01a93b551cf9

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