AERSMine - an adverse event data mining tool
by Global PharmacovigilanceA novel application utilising data from the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) has been developed by a Biomedical Informatics team at the Cincinnati Children’s Hospital Medical Center.
5th September 2016 •
comment
PAPER - an assessment of how adverse events from clinical trials are reported in published papers
by Global PharmacovigilanceA recently published paper in PLOS Medicine has investigated how adverse event data from clinical trials are summarised and consequently reported in published papers.
30th August 2016 •
comment