Add to ORKGBackground: Medical articles covering adverse drug events (ADEs) are systematically reported by pharmaceutical companies for drug safety information purposes. Although policies governing reporting to regulatory bodies vary among countries and regions, all medical article reporting may be categorized as precision or recall based. Recall-based reporting, which is implemented in Japan, requires the reporting of any possible ADE. Therefore, recall-based reporting can introduce numerous false negatives or substantial amounts of noise, a problem that is difficult to address using limited manual labor.Objective: Our aim was to develop an automated system that could identify ADE-related medical articles, support recall-based reporting, and alleviat...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
Background: Medical articles covering adverse drug events (ADEs) are systematically reported by phar...
INTRODUCTION: This work describes the Medication and Adverse Drug Events from Electronic Health Reco...
In the field of pharmacovigilance (PV), signal detection and assessment activities play a crucial ro...
In the field of pharmacovigilance (PV), signal detection and assessment activities play a crucial ro...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
The objective of this study was to determine whether the Food and Drug Administration’s Adverse Even...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
Background: Medical articles covering adverse drug events (ADEs) are systematically reported by phar...
INTRODUCTION: This work describes the Medication and Adverse Drug Events from Electronic Health Reco...
In the field of pharmacovigilance (PV), signal detection and assessment activities play a crucial ro...
In the field of pharmacovigilance (PV), signal detection and assessment activities play a crucial ro...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
The objective of this study was to determine whether the Food and Drug Administration’s Adverse Even...
<p>Multiple data sources are preferred in adverse drug event (ADEs) surveillance owing to inadequaci...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
The summary of product characteristics from the European Medicines Agency is a reference document on...
Post-marketing reports of suspected adverse drug reactions are important for establishing the safety...