Results 91 to 100 of about 136,694 (244)

Never events in UK general practice: a survey of the views of general practitioners on their frequency and acceptability as a safety improvement approach [PDF]

open access: yes, 2019
Background: Never events (NEs) are serious preventable patient safety incidents and are a component of formal quality and safety improvement (Q&SI) policies in the United Kingdom and elsewhere.
Alam, Rahul   +6 more
core   +2 more sources

Pattern and quality of scientific communications on drug safety produced by a regional pharmacovigilance center in Nepal

open access: yesPharmacy Practice, 2010
Analyzing the pattern and quality of scientific communications on pharmacovigilance can help the regional centers in Nepal and other developing countries to develop approaches for communicating effectively medicine safety issues. This kind of research is
Palaian S, Ibrahim MIM, Mishra P
doaj  

Evolução e elementos-chave do sistema de farmacovigilância do Brasil: uma revisão de escopo a partir da criação da Agência Nacional de Vigilância Sanitária

open access: yesCadernos de Saúde Pública, 2018
Esta revisão de escopo objetiva descrever e caracterizar o sistema de farmacovigilância do Brasil (SINAF) e averiguar o atendimento aos requisitos mínimos propostos pela Organização Mundial da Saúde para um desempenho funcional de sistemas nacionais ...
Daniel Marques Mota   +2 more
doaj   +1 more source

Learning signals of adverse drug-drug interactions from the unstructured text of electronic health records. [PDF]

open access: yes, 2013
Drug-drug interactions (DDI) account for 30% of all adverse drug reactions, which are the fourth leading cause of death in the US. Current methods for post marketing surveillance primarily use spontaneous reporting systems for learning DDI signals and ...
Bauer-Mehren, Anna   +4 more
core   +5 more sources

Intensive Monitoring Studies for Assessing Medicines: A Systematic Review

open access: yesFrontiers in Medicine, 2019
Introduction: Intensive monitoring (IM) is one of the methods of post-marketing active surveillance based upon event monitoring, which has received interest in the current medicines regulatory landscape. For a specific period of time, IM involves primary
Carla Torre   +10 more
doaj   +1 more source

Signal Detection of Adverse Drug Reaction of Amoxicillin Using the Korea Adverse Event Reporting System Database

open access: yesJournal of Korean Medical Science, 2016
We conducted pharmacovigilance data mining for a β-lactam antibiotics, amoxicillin, and compare the adverse events (AEs) with the drug labels of 9 countries including Korea, USA, UK, Japan, Germany, Swiss, Italy, France, and Laos. We used the Korea Adverse Event Reporting System (KAERS) database, a nationwide database of AE reports, between December ...
Mick Soukavong   +6 more
openaire   +3 more sources

BICEPP: an example-based statistical text mining method for predicting the binary characteristics of drugs

open access: yesBMC Bioinformatics, 2011
Background The identification of drug characteristics is a clinically important task, but it requires much expert knowledge and consumes substantial resources.
Tsafnat Guy   +4 more
doaj   +1 more source

Multi-Task Pharmacovigilance Mining from Social Media Posts

open access: yes, 2018
Social media has grown to be a crucial information source for pharmacovigilance studies where an increasing number of people post adverse reactions to medical drugs that are previously unreported.
Chowdhury, Shaika   +2 more
core   +1 more source

Spontaneous adverse drug reactions reported in a thirteen-year pharmacovigilance program in a tertiary university hospital

open access: yesFrontiers in Pharmacology
ObjectivesWe aimed to assess the characteristics of adverse drug reactions (ADRs) collected in a university hospital.MethodsA retrospective analysis of ADRs spontaneously reported in the Hospital Pharmacovigilance Program database (RutiRAM) over a 13 ...
E. Montané   +11 more
doaj   +1 more source

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