Objective: Driven by the need of pharmacovigilance centres and companies to routinely
collect and review all available data about adverse drug reactions (ADRs) and adverse …

Purpose Pharmacovigilance methods have advanced greatly during the last decades,
making post‐market drug assessment an essential drug evaluation component. These …

As new data sources have emerged, the data space which Pharmacovigilance (PV)
processes can use has significantly expanded. However, still, the currently available tools …

Background Pharmacovigilance aims to uncover and understand harmful side-effects of
drugs, termed adverse events (AEs). Although the current process of pharmacovigilance is …

Pharmacovigilance, the scientific discipline pertaining to drug safety, has been studied
extensively and is progressing continuously. In this field, medical informatics techniques and …

Pharmacovigilance plays a key role in the healthcare domain through the assessment,
monitoring and discovery of interactions amongst drugs and their effects in the human …

Abstract Information Technology (IT) and specialized systems could have a prominent role
towards the support of drug safety processes, both in the clinical context but also beyond …

Purpose: New pharmacovigilance methods are needed as a consequence of the morbidity
caused by drugs. We exploit fine-grained drug related adverse event information extracted …

Background Social media data are being increasingly used for population-level health
research because it provides near real-time access to large volumes of consumer-generated …

Background A hallmark of unregulated drug markets is their unpredictability and constant
evolution with newly introduced substances. People who use drugs and the public health …