The Information Extraction from clinical notes provides relevant information to identify adverse side effects in post-marketing surveillance of medications (Pharmacovigilance), which is more difficult to discover by traditional medical studies since patients are taking several treatments at the same time. In recent years, data mining techniques have allowed to discover knowledge stored in big datasets, such as the clinical records collected by hospitals throughout patient's life. The goal of this work is identify adverse side effects caused by treatments. Then, we have to identify relations between medications and Adverse Drug Events (ADE) entities, which is called Adverse Drug Reaction relation. This problem is divided Named Entity Recogni...
In medical domain, Adverse Drug Reaction (ADR) analysis is a crucial process for doctors and medical...
Adverse drug events (ADEs) are an important aspect of drug safety. Various texts such as biomedical ...
AbstractFor the purpose of post-marketing drug safety surveillance, which has traditionally relied o...
BACKGROUND: Pharmacovigilance and drug-safety surveillance are crucial for monitoring adverse drug e...
RÉSUMÉ: Un effet indésirable médicamenteux (EIM) peut être défini comme une réaction sensiblement no...
Adverse drug events (ADEs) as a set of detriments caused by medications, have led to additional medi...
BACKGROUND: Medication and adverse drug event (ADE) information extracted from electronic health rec...
This Work Presents A Two-Stage Deep Learning System For Named Entity Recognition (Ner) And Relation ...
© Springer Nature Switzerland AG 2018. Detection of new adverse drug reactions is intended to both i...
Adverse Drug Events (ADE) are injuries due to medication management rather than the underlying condi...
International audienceCurrently, the best performance for Named Entity Recognition in medical notes ...
The aim of this work is to infer a model able to extract cause-effect relations be-tween drugs and d...
Background: Pharmacovigilance and safety reporting, which involves processes for monitoring the use ...
Background: Pharmacovigilance and safety reporting, which involves processes for monitoring the use ...
© Springer International Publishing AG 2018. Adverse drug reactions can have serious consequences fo...
In medical domain, Adverse Drug Reaction (ADR) analysis is a crucial process for doctors and medical...
Adverse drug events (ADEs) are an important aspect of drug safety. Various texts such as biomedical ...
AbstractFor the purpose of post-marketing drug safety surveillance, which has traditionally relied o...
BACKGROUND: Pharmacovigilance and drug-safety surveillance are crucial for monitoring adverse drug e...
RÉSUMÉ: Un effet indésirable médicamenteux (EIM) peut être défini comme une réaction sensiblement no...
Adverse drug events (ADEs) as a set of detriments caused by medications, have led to additional medi...
BACKGROUND: Medication and adverse drug event (ADE) information extracted from electronic health rec...
This Work Presents A Two-Stage Deep Learning System For Named Entity Recognition (Ner) And Relation ...
© Springer Nature Switzerland AG 2018. Detection of new adverse drug reactions is intended to both i...
Adverse Drug Events (ADE) are injuries due to medication management rather than the underlying condi...
International audienceCurrently, the best performance for Named Entity Recognition in medical notes ...
The aim of this work is to infer a model able to extract cause-effect relations be-tween drugs and d...
Background: Pharmacovigilance and safety reporting, which involves processes for monitoring the use ...
Background: Pharmacovigilance and safety reporting, which involves processes for monitoring the use ...
© Springer International Publishing AG 2018. Adverse drug reactions can have serious consequences fo...
In medical domain, Adverse Drug Reaction (ADR) analysis is a crucial process for doctors and medical...
Adverse drug events (ADEs) are an important aspect of drug safety. Various texts such as biomedical ...
AbstractFor the purpose of post-marketing drug safety surveillance, which has traditionally relied o...