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active substance

Tilmicosin Phosphate — veterinary medicines

Authorised animal medicines containing Tilmicosin Phosphate 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.

Authorised products

25 authorised products across national registers.

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 Tilmicosin Phosphate, by species — reported counts, not proven reactions.

Cattle

825 reported events

openFDA

Top reactions: Death (473) · Lack of efficacy (bacteria) - NOS (174) · Collapse (see also 'Cardio-vascular' and 'Systemic disorders') (107) · Injection site swelling (99) · Recumbency (72)

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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