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Zambia
Handbook for Reporting Adverse Drug Reactions, Medication Errors, and Product Quality Problems
This handbook provides information on how to detect and report adverse drug reactions (ADRs) , medication errors, and product quality problems. It aims to facilitate and stimulate the active participation of healthcare workers in detecting and reporting these issues. The document was produced by the National Pharmacovigilance Unit (NPVU) under the Zambia Medicines Regulatory Authority (ZAMRA)
Use Cases
- Healthcare Workers: Provides guidance on detecting, assessing, and reporting adverse drug reactions, medication errors, and product quality problems. It serves as a tool to help them meet their professional responsibility to report suspected adverse events.
- National Pharmacovigilance Unit (NPVU): The document outlines the functions of the NPVU, including the collection, review, and evaluation of reports, as well as maintaining databases and providing feedback to reporters.
- Consumers/Patients: Advises consumers on how to report suspected adverse drug reactions to a healthcare worker or directly to ZAMRA.
- Pharmaceutical Industry: The document indicates that the NPVU receives reports from the pharmaceutical industry.
- Policy Makers: Data generated from ADR monitoring can assist the Zambia Medicines Regulatory Authority and policy makers in making evidence-based decisions.
Key takeaways you'll learn
