Aim: The aim was to evaluate the extent and factors responsible for underreporting (UR) of
adverse drug reactions (ADRs) in India. Materials and Methods: A retrospective …

Background This scoping review investigates the relationship between governance,
pharmacovigilance, and Agencia Nacional de Vigilancia Sanitaria (ANVISA) in Brazil, which …

Off-label prescribing of psychiatric drugs is common, despite lacking strong scientific
evidence of efficacy and potentially increasing risk for adverse events. The goal of this study …

Rationale, aims and objectives Pharmacovigilance (PV), or drug safety monitoring, aims to
improve patient safety through the detection and management of drug‐related adverse …

Background Adverse Drug Reactions (ADRs) are a major clinical and public health problem
world-wide. The prompt reporting of suspected ADRs to regulatory authorities to activate …

Background and aims: Under-reporting of adverse drug reactions (ADRs) by health-care
professionals (HCPs) is a worldwide problem. Spontaneous reporting in hospitals is scarce …

Pharmacovigilance is used to detect, assess, understand, and prevent the adverse effects of
medications. The need for safety monitoring has evolved around unfortunate incidents in …

ABSTRACT Objective: Adverse drug reactions (ADRs) can cause significant harm in
patients; however, ADRs are under-reported in many countries, including South Africa …

Aims The risk to develop adverse drug reactions (ADRs) is high for paediatric patients. This
is, amongst other reasons, due to the inevitable use of off-label and unlicensed medicines …

In the wake of the withdrawal of the nonsteroidal anti‐inflammatory drug rofecoxib,
regulators worldwide reconsidered their approach to postmarket safety. Many have since …