2,580 reported events
Top reactions: Deafness (896) · Lack of efficacy - NOS (814) · Vomiting (535) · Ataxia (412) · Head tilt - ear disorder (388)
15 authorised products across national registers.
United States — FDA Green Book
United Kingdom — VMD
Australia — APVMA PUBCRIS
No residue limits (MRL) are recorded for this substance.
No antimicrobial-resistance surveillance is recorded for this substance.
Spontaneous adverse-event reports that name Mometasone Furoate, by species — reported counts, not proven reactions.
Top reactions: Deafness (896) · Lack of efficacy - NOS (814) · Vomiting (535) · Ataxia (412) · Head tilt - ear disorder (388)
Top reactions: Ataxia (306) · Horner's syndrome (174) · Anorexia (160) · Head tilt - ear disorder (125) · Third eyelid protrusion (109)
Source: openFDA Animal & Veterinary adverse-event reports.
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