FOI2026/00964 - Librela adverse event reports
Published 12 August 2026
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1. Your request
I am seeking to obtain all adverse events reports submitted to VMD regarding Librela (bedinvetmab) from its date of approval in the UK to present.
2. Our reply
We have previously responded to a similar request, FOI2026/00324 which will be published on our disclosure log in due course. For your convenience, a copy of that response is attached.