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active substance

Prednisolone — veterinary medicines

Authorised animal medicines containing Prednisolone across national registers. Regulatory residue limits (MRL) and antimicrobial-resistance surveillance are shown when on record. This is a neutral reference and does not provide dosing or veterinary advice.
Reference information only — not veterinary advice and not a dosing source. Always consult a licensed veterinarian before giving any medicine to an animal.

Target species

BovinsVacheChevalCatsDogsHorsesCattleDog or cat

Authorised products

160 authorised products across national registers.

Italy — Ministero della Salute

United States — DailyMed (NLM)

Residue limits (MRL)

No residue limits (MRL) are recorded for this substance.

Antimicrobial resistance surveillance

No antimicrobial-resistance surveillance is recorded for this substance.

Reported adverse events (openFDA)

Spontaneous adverse-event reports that name Prednisolone, by species — reported counts, not proven reactions.

Cat

1,144 reported events

openFDA

Top reactions: Vomiting (183) · Lack of efficacy - NOS (150) · Weight loss (136) · Lethargy (see also Central nervous system depression in 'Neurological') (116) · Anorexia (113)

Source: openFDA Animal & Veterinary adverse-event reports.

Surveillance reference only — these are spontaneous adverse-event report counts, not proven adverse reactions, not causation and not a measure of any product's risk or safety. Always consult a licensed veterinarian.

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