UGC Approved Journal no 63975(19)
New UGC Peer-Reviewed Rules

ISSN: 2349-5162 | ESTD Year : 2014
Volume 12 | Issue 10 | October 2025

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 12 Issue 10
October-2025
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

Unique Identifier

Published Paper ID:
JETIR2510227


Registration ID:
570322

Page Number

c205-c211

Share This Article


Jetir RMS

Title

MONITORING ADVERSE DRUG REACTIONS (ADRS) AND RISK-BENEFIT ASSESSMENT

Abstract

Unintentional and dangerous reactions to drugs, known as adverse drug reactions (ADRs), present serious risks to patient safety and raise morbidity, mortality, and healthcare expenses globally. Pharmacovigilance is crucial for directing therapeutic choice and regulatory oversight, and it includes tracking adverse drug reactions (ADRs) and conducting systematic risk-benefit analyses. Inadvertent or slow signal detection, and inadequate coverage of everyday populations are the drawbacks of traditional ADR detection techniques, such as clinical trials and spontaneous reporting systems. Combining data exploration, machine learning, and computational intelligence techniques with different sources of data from medical professionals, patient-generated results, electronic medical files, and social media is becoming a potent strategy to improve ADR detection, anticipate risks, and maximize patient safety.. Proactive safety inspection and pharmacovigilance are further made possible by patient-centered approaches and continual tracking via wearable technology and mobile health (mHealth). This review emphasizes the significance of risk-benefit analysis, the current approaches and difficulties in ADR monitoring, and the revolutionary potential of statistical pharmacovigilance. Advanced analytics-backed integration of professional and individual patient data holds promise for enhancing signal detection, assisting clinical decision-making, and fortifying regulatory procedures globally

Key Words

Introduction,Adr Data Source,Risk–Benefit Assessment,Data Mining In Pharmacovigilance,.Challenges,.Future Perspectives, References.

Cite This Article

"MONITORING ADVERSE DRUG REACTIONS (ADRS) AND RISK-BENEFIT ASSESSMENT", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.12, Issue 10, page no.c205-c211, October-2025, Available :http://www.jetir.org/papers/JETIR2510227.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"MONITORING ADVERSE DRUG REACTIONS (ADRS) AND RISK-BENEFIT ASSESSMENT", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.12, Issue 10, page no. ppc205-c211, October-2025, Available at : http://www.jetir.org/papers/JETIR2510227.pdf

Publication Details

Published Paper ID: JETIR2510227
Registration ID: 570322
Published In: Volume 12 | Issue 10 | Year October-2025
DOI (Digital Object Identifier):
Page No: c205-c211
Country: Kolhapur, Maharashtra, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

00018

Print This Page

Current Call For Paper

Jetir RMS