Eurodrug Adverse Event Reporting
Introduction: Whether you are a patient, caregiver or healthcare professional, it is important to report adverse events for Eurodrug products.
The CIOMS Form must be completed within 24 h in case of a serious report.*
If the report is non-serious, the CIOMS Form must be completed within 72 h.
*In case the ADR is reported by another party to Eurodrug. That party is obliged to report to Eurodrug under the same timelines.
