Pharmacovigilance system in AUG Pharma
Pharmacovigilance is the process of collecting, monitoring, researching and evaluating information from healthcare providers and patients for the purposes of understanding and preventing drug-related problems.
ADVERSE EVENTS
Adverse Events (AEs) can be any unfavourable or unintended sign, symptom or disease temporarily associated with the use of a medicinal product, whether or not it is related to the product. Adverse Events can occur when medicines are used in any number of different circumstances. Healthcare providers and patients are encouraged to spontaneously report adverse events as a result of their experiences. Each is reviewed and follow up contacts are initiated when additional information is needed.
We are legally obligated
To follow up and report any adverse events that may have happened with any of its products.
@
Online Reporting
Adverse Events related to AUG Pharma products should also be reported directly to AUG Pharma via e-mail:
Any Adverse Events can be reported to the Egyptian Regulatory Authority via e-mail:
Reporting form for healthcare professionals (English form)
We are legally obligated
To follow up and report any adverse events that may have happened with any of its products.
@
Online Reporting
Adverse Events related to AUG Pharma products should also be reported directly to AUG Pharma via e-mail:
Any Adverse Events can be reported to the Egyptian Regulatory Authority via e-mail:
Reporting form for healthcare professionals (English form)
Adverse Events related to AUG Pharma products should also be reported directly to AUG Pharma via e-mail:
Any Adverse Events can be reported to the Egyptian Regulatory Authority via e-mail:
Reporting form for healthcare professionals (English form)