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At Sudair Pharma, patient safety is our highest priority. We are committed to monitoring, assessing, understanding, and preventing adverse drug reactions and other medicine-related issues. We encourage healthcare professionals, patients, and caregivers to report any suspected adverse events.
Need more information about our medicines, indications, dosage, or medical use?
If you experienced a side effect, please report it as soon as possible.
Access patient safety guidance materials
Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problems.
Every report helps improve patient safety and supports the safe use of medicines.
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”.
ADR is defined as “A noxious and unintended response to a medicine that occurs at normal therapeutic doses used in humans for the prophylaxis or therapy of disease.”
Reporting on the adverse drug reaction provide to us a very important reaction that help pharmacovigilance department in Sudair Pharma to analyze and make the right procedure to minimize the risk & provide a better guidance on how to use our products knowing that these reports will be sheared with the Saudi Food & Drug Authority (SFDA) to fulfill our responsibilities of reporting the adverse drug reaction.
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 the 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 will share the details of reported side effects with the Saudi Food & Drug Authority (SFDA) as mandated by law.
All health practitioners and members of society can report adverse events.
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Our medical information team is available to support healthcare professionals and patients.
Phone: 920001432
E-mail: medinfo@sudairpharma.com
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An adverse effect from SPC products must be reported.
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 through the concept of pharmacovigilance which is seeking to monitor, evaluate, & prevent any adverse event or any other drug problems through reporting.
Please contact us through online form, email or telephone. Our privacy notice outlines how SPC handles the processing of personal information when dealing with your enquiry, complaint or adverse event report.
Phone: +966 546030507
Tell us what happened. This should take about 3–5 minutes. Fields marked * are required.
Structured report intake for physicians, pharmacists and other HCPs. Fields marked * are required.
Monitoring, assessing, and preventing medicine-related harm.
Our Medical Information team is available to support healthcare professionals and patients.
920001432
medinfo@sudairpharma.com
An adverse effect from SPC products must be reported.
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 through the concept of Pharmacovigilance which is seeking to monitor, evaluate & prevent any adverse event or any other drug problems through reporting.
Please contact us through Online form, email or telephone. Our Privacy Notice outlines how SPC handles the processing of personal information when dealing with your enquiry, complaint or adverse event report.
+966 546030507
+966 920001432 Ext. 107
Pharmacovigilance@sudairpharma.com
