COMPOSITION:
Each ml contains:
Active Substance
Enrofloxacin 100.0 mg
Excipients
1-Butanol 30.0 mg
Pharmaceutical Form:
Solution for injection.
Clear, slightly yellowish to yellowish orange solution.
Indications for use, specifying the target species:
Cattle:
Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and secondary bacterial infections subsequent to viral infections (e.g., viral pneumonia), where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice.
Treatment of local signs (inflammation, milk quality and yield) associated with peracute/acute mastitis in lactating dairy cattle caused by E. coli, where herd history and previous sensitivity testing indicate enrofloxacin as the drug of choice.
Pigs:
Diseases of the respiratory and alimentary tract of bacterial or mycoplasmal origin (e.g. pasteurellosis, mycoplasmosis, coli-bacillosis, coli-septicaemia and salmonellosis) and multifactorial diseases such as atrophic rhinitis and enzootic pneumonia where clinical experience, supported where possible by sensitivity testing of the causal organism, indicates enrofloxacin as the drug of choice.
Contraindications:
Do not use the product for prophylaxis.
Do not use in cases of known hypersensitivity to fluoroquinolones or to any of the excipients.
Do not use when resistance / cross resistance to (fluoro)quinolones is known to occur.
Amounts to be administered and administration route:
To ensure correct dosage, body weight should be determined as accurately as possible to avoid underdosing.
Cattle:
For respiratory and alimentary infections in cattle and secondary bacterial infections: administer by subcutaneous injection.
• 2.5 mg enrofloxacin per kg bodyweight daily by subcutaneous injection for 3 days (2.5 ml per 100 kg bodyweight). This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for salmonellosis and complicated respiratory disease.
Not more than 10 ml should be administered at any one subcutaneous injection site.
For E. coli mastitis: administer by slow intravenous injection.
• 5.0 ml per 100 kg bodyweight (5 mg enrofloxacin per kg bodyweight) daily for 2 days.
Pigs:
For respiratory and alimentary infections in pigs and secondary bacterial infections: administer by intramuscular injection.
2.5 mg enrofloxacin per kg bodyweight) daily by intramuscular injection for 3 days (2.5 ml per 100 kg bodyweight). This rate may be doubled to 5 mg/kg bodyweight (5 ml per 100 kg) for 5 days for salmonellosis and complicated respiratory disease.
Not more than 2.5 ml should be administered at any one intramuscular injection site in store pigs or 5 ml at any one intramuscular injection site in sows.
Overdose (symptoms, emergency procedures, antidotes), if necessary:
Do not exceed the recommended dose. In accidental overdose there is no antidote and treatment should be symptomatic.
No signs of over dosage were observed in pigs following administration of the product at five times the recommended therapeutic dose.
Withdrawal Period(s):
Cattle: Subcutaneous use
Meat and offal: 10 days
Milk: 84 hours (7 milkings)
Cattle: Intravenous use
Meat and offal: 4 days
Milk: 72 hours (6 milkings)
Pigs: Intramuscular use
Meat and Offal 10 days
