Are consumers ready to take part in the Pharmacovigilance System?—a Portuguese preliminary study concerning ADR reporting

Author:

Matos Cristiano,van Hunsel Florence,Joaquim João

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,General Medicine

Reference32 articles.

1. Herdeiro MT, Figueiras A, Polónia J, Gestal-Otero J (2006) Influence of pharmacists’ attitudes on adverse drug reaction reporting. Drug Saf 29(4):331–340

2. Pal SN, Duncombe C, Falzon D, Olsson S (2013) WHO strategy for collecting safety data in public health programmes: complementing spontaneous reporting systems. Drug Saf 36(2):75–81

3. EC. Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance. Directive 2001/83/EC on the Community code relating to medicinal products for human us [online]. Available from URL: http://eur-lex.europa.eu/LexUriServ/LexUriServ.douri=OJ:L:2010:348:0074:0099:EN:PDF [Accessed 2011 May 30], 2010.

4. Aagaard L, Nielsen LH, Hansen EH (2009) Consumer reporting of adverse drug reactions: a retrospective analysis of the Danish adverse drug reaction database from 2004 to 2006. Drug Saf 32(11):1067–1074

5. van Hunsel FPAM (2011) The contribution of direct patient reporting to pharmacovigilance

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