editedbook
Publication: IIP Proceedings Year: 2022, Month: November Page No: 89-94, ISSN/ISBN: 978-93-95632-87-4, DOI/Link: https://rsquarel.org/assets/docupload/rsl2023180F24CC84B6C4D.pdf
OVERVIEW, STANDARD TERMS, AND DEFINITIONS IN PHARMACOVIGILANCE
Area/Stream: Pharmacy & Nursing, Authors: Prajwal Sharma Keywords: pharmacovigilance, drugs, overview, pharmacy, vigilance, clinical research, clinical trials, Book Name /series: Futuristic Trends in Pharmacy & Nursing, Volume 2, Book 25, Part 1, Chapter 8Publication: IIP Proceedings Year: 2022, Month: November Page No: 89-94, ISSN/ISBN: 978-93-95632-87-4, DOI/Link: https://rsquarel.org/assets/docupload/rsl2023180F24CC84B6C4D.pdf
Abstract:
AS per the definition from World Health Organization (WHO), Pharmacovigilance is defined as “the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.”Pharmacovigilance (PV) is a science or a process that is set up for safety monitoring of the medicines and drugs and then taking measures to maintain a positive benefit-to-risk ratio of the medicines. The knowledge of Adverse Drug Reactions can be expanded by several means such as Spontaneous reporting, database studies, and intensive monitoring. Several new processes are in development both at the scientific and regulatory level and are being developed keeping the strengthening of the PV system as the primary aim. On the scientific level, it includes increasing involvement of patients and transparency while on the regulatory level it includes risk management plans and conditional approval.
Cite this: Prajwal Sharma,"OVERVIEW, STANDARD TERMS, AND DEFINITIONS IN PHARMACOVIGILANCE", Futuristic Trends in Pharmacy & Nursing, Volume 2, Book 25, Part 1, Chapter 8, November, 2022, 89-94, 978-93-95632-87-4, https://rsquarel.org/assets/docupload/rsl2023180F24CC84B6C4D.pdf
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