Globally, adverse drug reactions (ADRs), one of the leading causes of morbidity and
mortality, will continue to pose a threat to public health as long as drugs are being used to …

Aim. To describe and synthesize aspects of knowledge, attitudes, and practice regarding
pharmacovigilance and adverse drug reaction (ADR) reporting and to explore associated …

Objective: The objective of the current study was to investigate the physician's knowledge,
attitude and practice towards pharmacovigilance. Methods: A mixed qualitative and …

Introduction: Pharmacovigilance (PV) is essential to detect and prevent adverse drug
reactions (ADR) after a drug is marketed. However, ADRs are significantly underreported …

Abstract Adverse Drug Reactions (ADRs) underreporting is a great challenge to
pharmacovigilance. Healthcare professionals should consider ADR reporting as their …

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 …

Context: Medication errors are the most common types of medical errors in hospitals and
leading cause of morbidity and mortality among patients. Aims: The aim of the present study …

Introduction Pharmacovigilance (PV) is critical in determining the risk–benefit ratio of
medicines and encouraging their safe, rational, and effective use, hence enhancing patient …

Background. The role of health care professionals among other stakeholders in early
detection, assessment, documentation, and reporting as well as preventing suspected …

Objectives To document the knowledge of, attitudes toward, and practices of adverse drug
reaction (ADR) reporting and pharmacovigilance systems among healthcare professionals …