FOI release

FOI ATI1119 - Adverse effect of Solensia

Published 5 January 2026

ATI1119 Request

Request for a specific adverse events report.

Our reply

Please find the requested report attached.

Please be aware that the sender report identification case reference number included in the report document is the internal reference number for this case in the VMD database, this may be different to the worldwide case number and/or Marketing Authorisation Holder’s internal reference number. Attached is a copy of the adverse event report that was received by VMD from the Marketing Authorisation Holder. Confidential and VMD or Marketing Authorisation Holder internal processing data have been redacted.

Adverse event report