Report An Adverse Event
The safety of patients is our highest priority.
If you become aware of a suspected adverse event associated with Novazepra®, please contact your healthcare provider and report the event to our pharmacovigilance team.
Please include the following information when possible:
- Patient initials
- Age and gender
- Description of the event
- Date of occurrence
- Product strength
- Country of use
Reports may be submitted via email to:
Email: pharmacovigilance@genoma-lab.ae
All reports are handled confidentially and in accordance with applicable pharmacovigilance regulations.