What is pharmacovigilance?
Pharmacovigilance is defined as “The science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems”.
What is adverse drug reaction (ADR)?
ADR is defined as “a response to a medicine which is noxious and unintended, and which occurs at doses normally used in man”.
Do drugs cause adverse drug reactions (ADRs)?
On the hypothetical side, all medications may cause some ADRs, but many people use drugs without causing them any ADRs. The benefit of taking a drug has generally outweigh the risk that may occur.
Why do we report adverse drug reaction?
Reporting the adverse drug reaction is considered a societal responsibility, and through that, you contribute in the collection of safety information process for each drug, so that IBSA GULF Pharmacovigilance Responsible Person(QPPV) can apply appropriate measures to minimize the reoccurrence of these ADRs.
The information you provide will also help us meet our responsibility for reporting Adverse Drug Reactions to regulatory authorities, which in turn will lead to improve the quality of health-care offered to the community.
Who can report?
All members of society can report ADRs.
All healthcare professionals including physicians, dentists, pharmacist, nurses and others, as well as patients can report ADRs
How to report ADRs?
Fill ADR reporting form either download PDF to handwritten or electronically and send it to Pharmacovigilance Dept.:
Alternatively, contact us and we will fill the form on behalf of you.
Our Contact Channels
Tel.: +966-11-462 9682 Extn. 105
Mobile: +966 554456187
If you would like to report ADR out of IBSA Gulf limited working hours, Please use the online Form or Call the 24hr mobile