Leveraging Routinely Collected Healthcare Data to Scale Up Drug Safety Surveillance: The EU-ADR Experience
Author:
Publisher
John Wiley & Sons, Ltd
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/9781118820186.ch28/fullpdf
Reference39 articles.
1. Harmonization process for the identification of medical events in eight European healthcare databases: the experience from the EU-ADR project;Avillach;J Am Med Inform Assoc,2013
2. Managing drug-risk information - what to do with all those new numbers;Avorn;N Engl J Med,2009
3. Automatic filtering and substantiation of drug safety signals;van Bauer-Mehren;PLoS Comput Biol,2012
4. Increasing scientific standards, independence and transparency in post-authorisation studies: the role of the European Network of Centres for Pharmacoepidemiology and Pharmacovigilance;Blake;Pharmacoepidemiol Drug Saf,2012
5. Early detection of adverse drug events within population-based health networks: application of sequential testing methods;Brown;Pharmacoepidemiol Drug Saf,2007
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