Adverse Event Following Immunization Electronic Report

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What is Pharmacovigilance?

Pharmacovigilance is a drug monitoring program established by WHO and defined as the science and activities relating to the detection, assessment, understanding, prevention and communication of adverse events of immunization, or any other vaccine, or issues related with immunization.

What is Adverse Event Following Immunization (AEFI)?

Any untoward medical occurrence which follows immunization and which does not necessarily have a causal relationship with the usage of the vaccine. The adverse event may be any unfavourable or unintended sign, abnormal laboratory finding, symptom or disease.

Why do we report AEFI?

Reporting is considered the cornerstone activity of pharmacovigilance, So by reporting the AEFI you will contribute in the safety information of ARABIO products to have a complete safety picture for our products and will be part in the pharmacovigilance process for improving the patient safety.

Who can report?

Everyone can report: Doctors, Pharmacists, Nurses, Patients and their relatives.

How to report?

Fill the AEFI report form electronically by clicking on the top link (we need to create electronic editable form) Or call the Pharmacovigilance responsible on the following contact details.

Contact us (24 / 7):
Mobile: +966558822193
Phone: 0114632384