Pharmacovigilance, the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug- related problems, is intrinsically linked to effective information management. The pivotal role of information in pharmacovigilance encompassing data collection, analysis, and dissemination for optimal patient safety. The foundation of pharmacovigilance lies in robust information system that facilitate the collection of adverse event reports from healthcare professionals, patients, and other stakeholder.
Every adverse event report, patient feedback, and clinical observation represents a piece of a larger safety puzzle. Without a robust information infrastructure, these insights risk being lost, delayed, or misinterpreted, which can compromise patient safety.
Effective information management is essential to pharmacovigilance, which is concerned with recognizing and preventing negative drug effects. To guarantee the highest level of patient safety, reliable information systems gather, examine, distribute, and publish reports from stakeholders, patients, and medical professionals.