Pharmacovigilance in Clinical Pharmacology: Ensuring Drug Safety and Monitoring Adverse Drug Reactions
Received Date: Apr 01, 2025 / Published Date: Apr 30, 2025
Abstract
Pharmacovigilance, the science and activities related to the detection, assessment, understanding, and prevention of adverse drug reactions (ADRs) and drug-related problems, is an essential component of clinical pharmacology. By systematically monitoring the safety of pharmaceuticals throughout their life cycle, pharmacovigilance ensures that the benefits of drugs outweigh their risks. This article explores the methodologies and practices employed in pharmacovigilance, reviews key findings regarding ADRs, and discusses their implications for patient safety and regulatory oversight. Through collaborative efforts among healthcare providers, regulatory authorities, and pharmaceutical industries, pharmacovigilance enhances the safety profile of medicines and promotes public health.
Citation: O芒聙聶Connor L (2025) Pharmacovigilance in Clinical Pharmacology: Ensuring Drug Safety and Monitoring Adverse Drug Reactions. Int J Res Dev Pharm L Sci, 11: 270. Doi: 10.4172/2278-0238.1000270
Copyright: 漏 2025 O鈥機onnor L. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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