A curated and standardized adverse drug event resource to accelerate drug safety research
A curated and standardized adverse drug event resource to accelerate drug safety research
Abstract Identification of adverse drug reactions (ADRs) during the post-marketing phase is one of the most important goals of drug safety surveillance. Spontaneous reporting systems (SRS) data, which are the mainstay of traditional drug safety surveillance, are used for hypothesis generation and to validate the newer approaches. The publicly available …