Post-marketing withdrawal of 462 medicinal products because of adverse drug reactions: a systematic review of the world literature

IJ Onakpoya, CJ Heneghan, JK Aronson - BMC medicine, 2016 - Springer
Background There have been no studies of the patterns of post-marketing withdrawals of
medicinal products to which adverse reactions have been attributed. We identified medicinal …

[HTML][HTML] Adverse drug reactions

JJ Coleman, SK Pontefract - Clinical Medicine, 2016 - Elsevier
Adverse drug reactions (ADRs) remain a challenge in modern healthcare, particularly given
the increasing complexity of therapeutics, an ageing population and rising multimorbidity …

Pharmacovigilance from social media: mining adverse drug reaction mentions using sequence labeling with word embedding cluster features

A Nikfarjam, A Sarker, K O'connor… - Journal of the …, 2015 - academic.oup.com
Objective Social media is becoming increasingly popular as a platform for sharing personal
health-related information. This information can be utilized for public health monitoring tasks …

[DOC][DOC] Dependence and withdrawal associated with some prescribed medicines

S Taylor, F Annand, P Burkinshaw… - London: Public …, 2019 - cdn.prgloo.com
Public Health England exists to protect and improve the nation's health and wellbeing, and
reduce health inequalities. We do this through world-leading science, research, knowledge …

The value of patient reporting to the pharmacovigilance system: a systematic review

P Inácio, A Cavaco, M Airaksinen - British journal of clinical …, 2017 - Wiley Online Library
Aims Current trends in pharmacovigilance systems are veering towards patient involvement
in spontaneous reporting of adverse drug reactions (ADRs). The aim of the current …

Data mining techniques in pharmacovigilance: analysis of the publicly accessible FDA adverse event reporting system (AERS)

E Poluzzi, E Raschi, C Piccinni… - Data mining applications …, 2012 - books.google.com
Drug use in medicine is based on a balance between expected benefits (already
investigated before marketing authorization) and possible risks (ie, adverse effects), which …

Pharmacovigilance in resource-limited countries

S Olsson, SN Pal, A Dodoo - Expert review of clinical …, 2015 - Taylor & Francis
In the past 20 years, many low-and middle-income countries have created national
pharmacovigilance (PV) systems and joined the WHO's global PV network. However, very …

[HTML][HTML] Causes for the underreporting of adverse drug events by health professionals: a systematic review

FR Varallo, SOP Guimarães, SAR Abjaude… - Revista da Escola de …, 2014 - SciELO Brasil
Objective: Identifying the main causes for underreporting of Adverse Drug Reaction (ADR)
by health professionals. Method: A systematic review carried out in the following databases …

Factors affecting patient reporting of adverse drug reactions: a systematic review

R Al Dweik, D Stacey, D Kohen… - British journal of clinical …, 2017 - Wiley Online Library
Aim The aim of the present study was to determine the barriers and motives influencing
consumer reporting of adverse drug reactions (ADRs). Methods A systematic review, guided …

Factors associated with underreporting of adverse drug reactions by patients: a systematic review

C Costa, P Abeijon, DA Rodrigues, A Figueiras… - International Journal of …, 2023 - Springer
Background Spontaneous reporting is the most used method to monitor post-marketing
safety information. Although patient involvement in spontaneous reporting has increased …