Results 31 to 40 of about 860,145 (127)
Extracting adverse drug reactions and their context using sequence labelling ensembles in TAC2017 [PDF]
Adverse drug reactions (ADRs) are unwanted or harmful effects experienced after the administration of a certain drug or a combination of drugs, presenting a challenge for drug development and drug administration. In this paper, we present a set of taggers for extracting adverse drug reactions and related entities, including factors, severity, negations,
arxiv
Adverse Drug Reactions: Knowledge, Attitude and Practice of Pharmacy
Background: Adverse Drug Reactions (ADRs) are one of the leading causes of morbidity and mortality and contribute to excessive health care costs. Detection and reporting of ADRs could decrease these consequences.
Maryam Etminani-Isfahani+5 more
doaj
An Exploratory Data Survey of Drug Name Incidence and Prevalence From the FDA's Adverse Event Reporting System, 2004 to 2012Q2 [PDF]
Drug Names, Population Level Surveillance and the FDA's Adverse Event Reporting System: An Exploratory Data Survey of Drug Name Incidence and Prevalence, 2004-2012Q2 Purpose: To count and monitor the drug names reported in the publicly available version of the Federal Adverse Event Reporting System (FAERS) from 2004 to 2012Q2 in a maximized sensitivity
arxiv
Background While medication labels are considered the authoritative resource for medication information, emerging research suggests that patient-generated health data (PGHD) are a valuable tool to understand the ways in which patients experience ...
David A. Blaser+6 more
doaj +1 more source
BackgroundRobust adverse drug event (ADE) reporting systems are crucial to monitor and identify drug safety signals, but the quantity and type of ADEs captured may vary by system characteristics.
Erica Y Lau+4 more
doaj +1 more source
Multi-Task Learning for Extraction of Adverse Drug Reaction Mentions from Tweets [PDF]
Adverse drug reactions (ADRs) are one of the leading causes of mortality in health care. Current ADR surveillance systems are often associated with a substantial time lag before such events are officially published. On the other hand, online social media such as Twitter contain information about ADR events in real-time, much before any official ...
arxiv
Pharmacovigilance and drug safety 2011 in Calabria (Italy): Adverse events analysis
Background : Pharmacovigilance assesses the safety profile of drugs. Its main aim is the increase of spontaneous reporting of adverse drug reactions (ADRs). The Italian Drug Agency (AIFA; Agenzia Italiana del Farmaco) is financing several projects to the
Francesca Scicchitano+18 more
doaj
Evaluation of anti-tuberculosis induced adverse reactions in hospitalized patients
Background: Tuberculosis has been one of the common diseases of human communities. Besides of disease-related complications, there are serious adverse reactions due to Anti-tuberculosis (Anti-TB) drug therapy.
Gholami K+3 more
doaj
Yellow Fever Virus Vaccine–associated Deaths in Young Women
Yellow fever vaccine–associated viscerotropic disease is a rare sequela of live-attenuated virus vaccine. Elderly persons and persons who have had thymectomies have increased susceptibility.
Stephen J. Seligman
doaj +1 more source
Comparison of Patient Adverse Drug Reaction Reporting Systems in Nine Selected Countries. [PDF]
Worakunphanich W+4 more
europepmc +1 more source