Pharmacovigilance: Ensuring Drug Safety and Monitoring Adverse Effects

Abstract

Pharmacovigilance plays a crucial role in safeguarding 
public health by identifying, assessing, and preventing  adverse effects of pharmaceutical products. This  abstract provides an overview of pharmacovigilance,  highlighting its significance in ensuring drug safety  throughout the lifecycle of a medicine.
Pharmacovigilance involves systematic monitoring,  collection, assessment, and analysis of adverse drug  reactions (ADRs) following the introduction of a medication into the market. The primary objective is to detect potential risks associated with the use of drugs 
and to take appropriate regulatory actions to minimize  harm. Various stakeholders contribute to  pharmacovigilance, including pharmaceutical  companies, regulatory authorities, healthcare  professionals, and patients. Collaboration among these stakeholders is essential for the timely detection and reporting of ADRs, which ultimately enhances patient safety.