We Sudair Pharma collaborate with the Health practitioners to put patient safety in our first priorities to provide Integrated health care based on high-quality throw concept of the Pharmacovigilance Which Seeks to monitor, evaluation & Prevent any adverse event or any other drug problems throw by reporting.

The Saudi Food & Drug Authorities (SFDA) & Ministry of Health (MOH) in Saudi Arabia & other Supervisory authority in Gulf Country & All the World have some Legal requirements that control how to deal with the adverse event of medicinal products.

What is pharmacovigilance?

Pharmacovigilance is defined by world health organization as “The science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems”.

What is the benefit of reporting ADR?

Reporting on the adverse drug reaction provide to us a very important reaction that help pharmacovigilance responsible reason in Sudair Pharma to make the right procedure to minimize the risk & provide a better guidance on how to use our products knowing that these reports will be shared with the Saudi Food & Drug Authority (SFDA) to fulfill our responsibilities of reporting the adverse drug reaction which will improve the quality of the health care system.

What is the benefit of reporting ADR?

Reporting on the adverse drug reaction provide to us a very important reaction that help pharmacovigilance responsible reason in Sudair Pharma to make the right procedure to minimize the risk & provide a better guidance on how to use our products knowing that these reports will be shared with the Saudi Food & Drug Authority (SFDA) to fulfill our responsibilities of reporting the adverse drug reaction which will improve the quality of the health care system.

How does Sudair Pharma handle the privacy of reported adverse drug reaction (ADR)?

All personal information related to the reporting of an adverse drug reaction is processed in accordance with the data protection legislation. Your report is used solely for the scientific evaluation of medicine. After careful evaluation of each report received, it will be filed in our safety database and regularly used to look for overall patterns. Sudair Pharma may share the details of reported side effects with the Saudi Food & Drug Authority (SFDA) as mandated by law.

Who can report adverse drug reaction?

All members of society can report adverse events.

How to report an adverse drug reaction?

You can use the electronic way through our website and once you click “send”, it will go to the pharmacovigilance department in Sudair Pharma.
Alternatively, contact us through the below details and we will fill the form on behalf of you.

Pharmacovigilance Department

Tell:       +966 920001432 Ext. 107

Mobile: +966 546030507

Email:    Pharmacovigilance@sudairpharma.com

Adverse Drug Reaction Reporting Form

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