1,081 reported events
Top reactions: Death (359) · Lack of efficacy - NOS (277) · Behavioural disorder NOS (234) · Hypersalivation (183) · Not eating (173)
4 authorised products across national registers.
France — ANSES-ANMV
United States — DailyMed (NLM)
United States — FDA Green Book
No residue limits (MRL) are recorded for this substance.
No antimicrobial-resistance surveillance is recorded for this substance.
Spontaneous adverse-event reports that name Dexmedetomidine, by species — reported counts, not proven reactions.
Top reactions: Death (359) · Lack of efficacy - NOS (277) · Behavioural disorder NOS (234) · Hypersalivation (183) · Not eating (173)
Source: openFDA Animal & Veterinary adverse-event reports.
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