The Quality of Clinical Information in Adverse Drug Reaction Reports by Patients and Healthcare Professionals: A Retrospective Comparative Analysis

Author:

Rolfes LeànORCID,van Hunsel Florence,van der Linden Laura,Taxis Katja,van Puijenbroek Eugène

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology,Toxicology

Reference38 articles.

1. World Health Organization. The importance of pharmacovigilance: safety monitoring of medicinal products. 2002 [cited 2016 Dec 1]. http://apps.who.int/medicinedocs/en/d/Js4893e/ .

2. US Food and Drug Administration. FDA adverse events reporting system (FAERS). 2016. [cited 2016 Feb 25]. http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/UCM082196 .

3. Ishiguro C, Hall M, Neyarapally GA, Dal PG. Post-market drug safety evidence sources: an analysis of FDA drug safety communications. Pharmacoepidemiol Drug Saf. 2012;21(10):1134–6.

4. van Hunsel F, Härmark L, Pal S, Olsson S, van Grootheest K. Experiences with adverse drug reaction reporting by patients; an 11-country survey. Drug Saf. 2012;35(1):45–60.

5. The EU pharmacovigilance system. 2012 [cited 2016 Feb 17]. http://ec.europa.eu/health/human-use/pharmacovigilance/index_en.htm .

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