Guideline For Adverse Drug Reactions (ADRs) Reporting for Healthcare Professionals

Guideline For Adverse Drug Reactions (ADRs) Reporting for Healthcare Professionals

This document has been prepared to serve as a guideline to healthcare professionals reporting adverse drug reactions, adverse event following immunisations and product quality problems. It represents South African Health Products Regulatory Authority’s (SAHPRA’s) current thinking on the safety, quality and efficacy of medicines.

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Document Number: SAHPGL-CEM-PV-06
Version: 3
Date Updated: 18/08/2022
File Type: pdf
Category: Guideline
Unit: Pharmacovigilance