Pharmacovigilance
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Patient Safety
Pharmacovigilance
If you have experienced or observed an adverse drug reaction (ADR) related to a Luminar product, please report it immediately. All reports are handled confidentially and in accordance with international pharmacovigilance standards.
Direct ADR Reporting
For urgent safety reports, email our pharmacovigilance team directly:
pv@luminarlife.com
Note: Pharmacovigilance reporting is a regulatory obligation. Please include product name, batch number (if available), description of the adverse event, and patient information in your report.
Online ADR Report
Submit an adverse drug reaction report using the form below.
Submit ADR Report via EmailClicking the button will open your email client with a pre-filled ADR report template addressed to our pharmacovigilance team.