Země: Velká Británie
Jazyk: angličtina
Zdroj: VMD (Veterinary Medicines Directorate)
Flunixin
MSD Animal Health UK Limited
QM01AG90
Flunixin
Oral paste
POM-V - Prescription Only Medicine – Veterinarian
Horses
Anti Inflammatory NSAID
Authorized
1989-02-02
Revised: October 2022 AN: 01265/2022 Page 1 of 5 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Finadyne 50 mg/g Oral Paste 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each gram contains: ACTIVE SUBSTANCE: Flunixin 50 mg as flunixin meglumine 83 mg EXCIPIENTS: For the full list of excipients, see section 6.1 3. PHARMACEUTICAL FORM Oral paste. White to off-white paste. 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Horses. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES For the alleviation of inflammation and pain associated with musculoskeletal disorders in the horse. 4.3 CONTRAINDICATIONS Do not exceed the stated dose or duration of treatment. Do not use in animals suffering from cardiac, hepatic or renal disease, or where there is the possibility of gastrointestinal ulceration or bleeding. Do not use in cases of hypersensitivity to the active substance. Do not administer steroidal or other non-steroidal anti-inflammatory drugs concurrently or within 24 hours of each other. Do not use in hypovolaemic animals except in the case of endotoxaemia or septic shock. 4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES Non-steroidal anti-inflammatory drugs are not permitted substances under the rules of racing and under rules covering other competitive events. The Royal College of Revised: October 2022 AN: 01265/2022 Page 2 of 5 Veterinary Surgeons has given guidance to the Veterinary profession regarding the use of anti-inflammatory drugs in competing horses. It states that if a veterinarian recommends the discontinuation of any such drug not less than eight days before racing he should feel sure he has catered for all but the most exceptional case. 4.5 SPECIAL PRECAUTIONS FOR USE Special precautions for use in animals: Use in animals less than 6 weeks of age or in aged animals may involve additional risk. If such use cannot be avoided animals may require a reduced dosage and careful clinical management. In animals undergoing general anaesthesia it is preferable to wait until they are fully r Přečtěte si celý dokument