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Speaking the Same Language: The Need for Accurate and Consistent Reporting of Novel Per- and Polyfluoroalkyl

Benjamin J Place1, Jared M Ragland2

  • 1Chemical Sciences Division, National Institute of Standards & Technology, Gaithersburg, Maryland 20850, United States.

Environmental Science & Technology
|July 18, 2022
PubMed
Abstract

No abstract available in PubMed .

Keywords:
PFASnomenclaturenovel

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Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
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