Pharmacovigilance: There is a Need for All to Get Involved!

Baah, Emmanuel M. (2018) Pharmacovigilance: There is a Need for All to Get Involved! Asian Journal of Research in Medical and Pharmaceutical Sciences, 5 (1). pp. 1-11. ISSN 24570745

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Abstract

The harm(s) a drug may cause may not be known at the time it gains market authorisation. Drug regulatory agencies weigh the benefits that the drug presents against the potential harms it could pose and allow it to be marketed if it is believed that the drug has a favourable risk-benefit ratio. Regulatory agencies then evaluate the drug’s risk profile as it is used on a large scale and institute remedial measures if found necessary. Data is needed in establishing that an Adverse Event (AE) accompanying drug use is, in fact, an Adverse Drug Reaction (ADR), and in carrying out the functions outlined above. This paper explores some of the issues involved, the importance of data in the work of regulatory agencies and draws attention to the need for all to facilitate the work of regulatory agencies.

Item Type: Article
Subjects: STM Digital Press > Medical Science
Depositing User: Unnamed user with email support@stmdigipress.com
Date Deposited: 27 Apr 2023 11:21
Last Modified: 03 Sep 2024 05:20
URI: http://publications.articalerewriter.com/id/eprint/674

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