Background Spontaneous reporting is the most used method to monitor post-marketing
safety information. Although patient involvement in spontaneous reporting has increased …

Objective Patients with rare cancers may experience different unmet needs than those with
common cancer. The objective of this systematic review was to (1) investigate unmet …

Background Healthcare professionals' involvement and reporting of adverse drug reactions
are essential for the success of a pharmacovigilance program. The aim of this study was to …

Introduction The aim of this study was to evaluate the effectiveness of interventions used for
improving ADR reporting by patients and healthcare professionals. Areas covered A …

Background Spontaneous reporting of adverse drug reactions (ADRs) is a method of
monitoring the safety of drugs and is the basic strategy for the post-marketing surveillance of …

Introduction Adverse drug reaction (ADR) under-reporting is highly prevalent internationally
and interventions created to address this problem have only been temporarily successful …

Background: Spontaneous reporting systems are the commonest means of reporting
adverse drug reactions (ADRs) worldwide. Under-reporting remains a challenge particularly …

All medicinal products authorized in the European Union are subjects of constant drug-
safety monitoring processes. It is organized in a pharmacovigilance system that is designed …

Objective This study aimed to assess the knowledge, attitude and practice of adverse drug
reactions (ADRs) reporting and identify factors associated with ADRs reporting among …

This study aimed to investigate the current knowledge and experiences of consumers in
Australia on adverse drug reaction (ADR) reporting and their reasons for reporting or not …