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active substance

Oxytetracycline Dihydrate — veterinary medicines

Authorised animal medicines containing Oxytetracycline Dihydrate 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

Dogs

Authorised products

5 authorised products across national registers.

Australia — APVMA PUBCRIS

United Kingdom — VMD

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 Oxytetracycline Dihydrate, by species — reported counts, not proven reactions.

Cattle

88 reported events

openFDA

Top reactions: Death (63) · Lack of efficacy (bacteria) - NOS (26) · Lack of efficacy - NOS (24) · Injection site swelling (18) · Anaphylaxis (17)

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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