3,862 reported events
Top reactions: INEFFECTIVE, SEDATION (741) · Bradycardia (480) · Lack of efficacy - NOS (465) · Death (322) · Vomiting (318)
37 authorised products across national registers.
United Kingdom — VMD
United States — DailyMed (NLM)
Canada — Health Canada DPD
Australia — APVMA PUBCRIS
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 Hydrochloride, by species — reported counts, not proven reactions.
Top reactions: INEFFECTIVE, SEDATION (741) · Bradycardia (480) · Lack of efficacy - NOS (465) · Death (322) · Vomiting (318)
Top reactions: Death (214) · INEFFECTIVE, SEDATION (156) · Lack of efficacy - NOS (146) · Hypersalivation (140) · Cardiac arrest (123)
Source: openFDA Animal & Veterinary adverse-event reports.
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