Pharmacovigilance

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem.

All medicines and vaccines undergo rigorous testing for safety and efficacy through clinical trials before they are authorized for use. However, the clinical trial process involves studying these products in a relatively small number of selected individuals for a short period of time. Certain side effects may only emerge once these products have been used by a heterogenous population, including people with other concurrent diseases, and over a long period of time.

On this page, colleagues can report voluntarily (voluntary reporting) if there is a suspicion of side effects and drug safety by filling in the fields provided in the website display below. We will report the results of the "pharmacovigilance" reporting from our colleagues/medical personnel to the relevant parties for further action. Therefore, it is requested to be able to fill in the data completely and correctly.

Reference:
WHO. What is Pharmacovigilance? [Internet]. Available from: https://www.who.int/teams/regulation-prequalification/regulation-and-safety/pharmacovigilance

Note: The data entered will be kept confidential