Species: All mammalian food producing species
No MRL required
European Union
Species: All mammalian food producing species
active substance
Dinoprost Tromethamine — veterinary medicines
Authorised animal medicines containing Dinoprost Tromethamine 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
7 authorised products across national registers.
United States — DailyMed (NLM)
United States — FDA Green Book
Residue limits (MRL)
Antimicrobial resistance surveillance
No antimicrobial-resistance surveillance is recorded for this substance.
Reported adverse events (openFDA)
Spontaneous adverse-event reports that name Dinoprost Tromethamine, by species — reported counts, not proven reactions.
Cattle
907 reported events
openFDA
Top reactions: INEFFECTIVE, ESTRUS SYNCHRONIZ (290) · Lack of efficacy - NOS (231) · Death (226) · Injection site swelling (177) · Myositis (60)
Horse
61 reported events
openFDA
Top reactions: Hyperhidrosis (14) · Death (10) · Abdominal pain (9) · INEFFECTIVE, ESTRUS SYNCHRONIZ (8) · Accidental exposure (7)
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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