What is Pharmacovigilance?
Pharmacovigilance is a program designed to monitor medications and their associated risks. The World Health Organization (WHO) established this program, defining it as: “The science and activities related to the detection, assessment, understanding, and prevention of adverse drug effects or any other drug-related problems.”
What are Adverse Event?
Adverse Event are unintended and undesirable effects that may sometimes occur when using pharmaceutical products at their correct dosage.
Why Should You Report Adverse Event?
Reporting is considered the cornerstone activity of pharmacovigilance, so by reporting the AE you will contribute in the safety information of DEEF pharma 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 Adverse Event?
Anyone in the community can report Adverse Event, including:
- Doctors
- Pharmacists
- Healthcare nurses
- Patients or their caregivers
How to report?How to Report Adverse Event?
You can report Adverse Event by filling out the online form by clicking the link above or by contacting the pharmacovigilance officer through the following communication channels: