Surveillance of pharmacovigilance, also known as drug safety surveillance, involves the
monitoring and evaluation of drug-related adverse events or side effects to ensure the safe …

Pharmacovigilance is a science that involves the ongoing monitoring of adverse drug
reactions to existing medicines. Traditional approaches in this field can be expensive and …

Introduction Pharmacovigilance (PV) involves monitoring and aggregating adverse event
information from a variety of data sources, including health records, biomedical literature …

As defined by the World Health Organization (WHO), pharmacovigilance encompasses a
range of activities whose common aim is to detect and prevent any possible drug-related …

Pharmacovigilance is a systematic and scientifically rigorous discipline that assumes
responsibility for the safety of pharmaceuticals, with its primary objective being the mitigation …

The goal of pharmacovigilance is to detect, monitor, characterize and prevent adverse drug
events (ADEs) with pharmaceutical products. This article is a comprehensive structured …

Adverse drug events (ADEs) are unexpected incidents caused by the administration of a
drug or medication. To identify and extract these events, we require information about not …

Objective This article presents our approaches to extraction of medications and associated
adverse drug events (ADEs) from clinical documents, which is the second track of the 2018 …

Drug‐drug interactions (DDIs) are one of the indispensable factors leading to adverse event
reactions. Considering the unique structure of AERS (Food and Drug Administration …

Abstract Adverse Drug Events (ADEs) are common and occur in approximately 2-5% of
hospitalized adult patients. Each ADE is estimated to increase healthcare cost by more than …