Reporting Adverse Events

Last Updated on February 28, 2023

National Pharmacovigilance Centre, DRAP collects reports of suspected Adverse Events associated with the use of therapeutic products. Anyone can report a suspected adverse events.

DRAP has enabled both electronic and manual systems for collection of reports of suspected adverse events:-

Med Vigilance E Reporting

Med Safety Mobile App

Yellow Reporting Form/
Suspected Adverse Drug Reaction Reporting Form

Following ways can be used to report a suspected adverse events:-

Ask your healthcare professional (Physicians, Pharmacists and Nurses), to report a side effect or adverse reaction.

Report Your Side Effect or Adverse Reaction by Yourself to National Pharmacovigilance Centre through Med Vigilance System of DRAP

Download and fill out a yellow reporting form and send to National Pharmacovigilance Centre of DRAP through email at npc∂dra.gov.pk or at postal address.

For further information about who can report ADRs and how to report suspected Adverse Events to DRAP, please navigate to How to Report ADRs to DRAP