Report an Adverse Event. CSL collects information on adverse events to be able to monitor product safety and to investigate, evaluate and report adverse effects to applicable authorities.

To report an adverse event, contact us here or report via the Norwegian Medical Products Agency (Direktoratet for Medisinske produkter)

When you report a suspected adverse event, we collect certain personal data. If you submit a report within the EU, you can read more about how we handle your personal data here: Privacy Notice for Reporting Suspected Side Effects within Europe and GDPR.