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ADR Monitoring and Pharmacovigilance by Dipankar Nath is a document available to read on EtoBox.

This document discusses adverse drug reaction (ADR) monitoring and pharmacovigilance. It defines an ADR and explains that ADRs are a major health issue, causing deaths and increased healthcare costs. The key aspects of ADR monitoring discussed are identifying ADRs, assessing the relationship between drugs and reactions, documenting ADRs, and reporting serious ADRs. ADR monitoring can occur during drug development through clinical trials, but most ADRs are identified after approval through spontaneous report

Author
Dipankar Nath
Language
EN