TARGET SPECIES: Cattle, sheep, goats, pigs.
INDICATIONS: Cattle: the treatment of respiratory tract infections caused by enrofloxacin-sensitive strains of Pasteurella multocida, Mannheimia haemolytica and Mycoplasma spp. The treatment of severe acute mastitis caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of digestive tract infections caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of sepsis caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of arthritis associated with acute mycoplasmosis caused by enrofloxacin-sensitive strains of Mycoplasma bovis in cattle younger than 2 years of age.
Sheep: The treatment of digestive tract infections caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of sepsis caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of mastitis caused by enrofloxacin-sensitive strains of Staphylococcus aureus and Escherichia coli.
Goats: The treatment of respiratory tract infections caused by enrofloxacin-sensitive strains of Pasteurella multocida, Mannheimia haemolytica and Mycoplasma spp. The treatment of digestive tract infections caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of sepsis caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of mastitis caused by enrofloxacin-sensitive strains of Staphylococcus aureus and Escherichia coli.
Pigs: The treatment of respiratory tract infections caused by enrofloxacin-sensitive strains of Pasteurella multocida, Mycoplasma spp. and Actinobacillus pleuropneumoniae. The treatment of urinary tract infections caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of digestive tract infections caused by enrofloxacin-sensitive strains of Escherichia coli. The treatment of sepsis caused by enrofloxacin-sensitive strains of Escherichia coli.
1 ml of solution for injection contains:
Active substance:
Enrofloxacin……………………………………………………100 mg
Excipients: n-butyl alcohol, potassium hydroxide, water for injections.
CONTRAINDICATIONS:
Do not administer in case of hypersensitivity to the active substance or any of the excipients.
Do not use in growing horses because it can cause possible conditions of the articular cartilage.
ADVERSE REACTIONS:
Except for potential joint disorders in growing cartilages in immature animals, adverse reactions are rather rare. Transient edema may occur at the site of inoculation. If you notice any serious reactions or other effects not listed in this leaflet, please inform your veterinarian.
METHOD OF ADMINISTRATION:
Intravenous, subcutaneous or intramuscular administration.
Repeated injections should be performed at different injection sites.
Cattle:
5 mg of enrofloxacin/kg bw, which corresponds to 1 ml of product/20 kg bw, once a day, for 3-5 days. Arthritis associated with acute mycoplasmosis caused by enrofloxacin-sensitive strains of Mycoplasma bovis in cattle aged less than two years: 5 mg of enrofloxacin/kg bw, which corresponds to 1 ml of product/20 kg bw, once a day, for 5 days. The product may be administered by slow intravenous or subcutaneous injection. Acute mastitis caused by Escherichia coli: 5 mg of enrofloxacin/kg bw, corresponding to 1 ml of product/20 kg bw, by slow intravenous injection, once a day, for two consecutive days. A second dose can be administered subcutaneously. In this case, the withdrawal period after subcutaneous injection applies. No more than 10 ml should be administered in a single subcutaneous injection site..
Sheep and goats:
5 mg of enrofloxacin/kg bw, which corresponds to 1 ml of product/20 kg bw, once a day, by subcutaneous injection, for 3 days. No more than 6 ml should be administered in a single subcutaneous injection site.
Pigs:
2.5 mg of enrofloxacin/kg bw, which corresponds to 0.5 ml of product/20 kg bw, once a day, by intramuscular injection, for 3 days. Infections of the digestive tract or sepsis caused by Escherichia coli: 5 mg of enrofloxacin/kg bw, which corresponds to 1 ml of product/20 kg bw, once a day, by intramuscular injection, for 3 days. In pigs, the injection should be done in the neck area, at the base of the ear. No more than 3 ml should be administered in a single intramuscular injection site.
RECOMMENDATIONS FOR PROPER ADMINISTRATION:
In order to ensure proper dosage, the body weight (bw) should be determined as accurately as possible to avoid under-dosing.
WITHDRAWAL PERIOD:
Cattle:
After the intravenous injection: meat and offal: 5 days; milk: 3 days.
After the subcutaneous injection: meat and offal: 12 days; milk: 4 days.
Sheep: meat and offal: 4 days; milk: 3 days.
Goats: meat and offal: 6 days; milk: 4 days.
Pigs: meat and offal: 13 days.
STORAGE:
Keep out of the reach and sight of children. Store at temperatures lower than 25°C. Keep away from direct sunlight and frost. Do not use after the product expiration date stated on the label. Shelf life after first opening the primary packaging: 28 days.