Identifying and managing adverse drug reactions: Qualitative analysis of patient reports to the UK yellow card scheme
Author:
Affiliation:
1. Royal College of Surgeons in Ireland (RCSI) Dublin Ireland
2. Medway School of Pharmacy Universities of Greenwich and Kent UK
3. College of Medical and Dental Sciences University of Birmingham Birmingham UK
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bcp.15263
Reference33 articles.
1. European Union pharmacovigilance legislation.Regulation (EU) No520/2012.2012. Available at:https://www.ema.europa.eu/en/human-regulatory/overview/pharmacovigilance/legal-framework/implementation-pharmacovigilance-legislation
2. Fifteen years of patient reporting –what have we learned and where are we heading to?
3. World Health organisation.Patient safety.2019. Available at:https://www.who.int/news-room/fact-sheets/detail/patient-safety
4. On the assessment of adverse drug reactions from spontaneous reporting systems: the influence of under-reporting on odds ratios
5. The value of patient reporting to the pharmacovigilance system: a systematic review
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