Pharmacovigilance

ADRs & AEFIs Reporting

Please report ALL suspected Adverse Drug Reactions (ADRs) and Adverse Events Following Immunization (AEFIs) to NAROVAC. Your reports help us monitor the safety of our vaccine and improve animal health outcomes.

How to report a suspected reaction

If you observe an adverse drug reaction or an adverse event following immunization, please report it to NAROVAC as soon as possible using any of the channels below, or scan the QR code to access the reporting form.

Contact NAROVAC

Open the ADR/AEFI Reporting Form

Scan to report

Scan the QR code with your phone to open the ADR/AEFI reporting form.

QR code for ADR/AEFI reporting https://npes.ulsportal.or.ug/adr-report

Reporting a suspected reaction helps NAROVAC and regulators monitor product safety. It does not replace veterinary advice. Contact a qualified veterinary professional for advice about a specific animal or herd.

Pharmacovigilance Notice

Report all suspected Adverse Drug Reactions (ADRs) and Adverse Events Following Immunization (AEFIs):

039 3104369 / 0800 111 811
Report an ADR/AEFI