Reporting Adverse Events

Last Updated on July 22, 2022

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:-

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