ENROFLOXACYNA VETOS-FARMA 50 mg / 1 ml

Description

solution for injection for cattle, pigs, dogs and cats

The name of the veterinary medicinal product:
Enrofloxacin Vetos-Farma, 50 mg / 1 ml, solution for injection for cattle, pigs, dogs and cats.

Content of active substance and other substances:
1 ml of the product contains: active substance: enrofloxacin 50 mg; excipient: butanol 30 mg.

Therapeutic indications:
Calves: Treatment of respiratory tract infections caused by enrofloxacin susceptible strains Pasteurella multocida, Mannheimia haemolytica and Mycoplasma spp. Treatment of gastrointestinal infections caused by enrofloxacin susceptible Escherichia coli strains. Treatment of sepsis caused by enrofloxacin susceptible strains of Escherichia coli. Treatment of acute mycoplasma arthritis caused by enrofloxacin susceptible strains of Mycoplasma bovis. Pigs: Treatment of respiratory tract infections caused by enrofloxacin susceptible strains Pasteurella multocida, Mycoplasma spp. And Actinobacillus pleuropneumoniae. Treatment of gastrointestinal infections caused by enrofloxacin susceptible strains of Escherichia coli. Treatment of sepsis caused by enrofloxacin susceptible strains of Escherichia coli. Dogs: Treatment of gastrointestinal, respiratory and genitourinary infections (including prostatitis, supportive antibiotics for ropomacic treatment), skin and wound infections, otitis (external / middle) infections caused by enrofloxacin susceptible strains of Staphylococcus spp. Escherichia coli, Pasteurella spp., Klebsiella spp., Bordetella spp., Pseudomonas spp. And Proteus spp. Cats: Treatment of infections of the digestive system, respiratory tract and genitourinary tract (including antibiotic therapy in the treatment of ropomacosis), skin infections and wounds, Caused by enrofloxacin susceptible strains: Staphylococcus spp., Escherichia coli, Pasteurella spp., Klebsiella spp., Bordetella spp., Pseudomonas spp. And Proteus spp.

Contraindications:
Do not use prophylactically. Do not use in dogs less than 1.5 years of age, especially in dogs of large fast-growing breeds, due to the possibility of damage to the articular cartilage. Do not use in cats less than 8 weeks of age. Not used in the case of known resistance / cross-resistance to fluoroquinolones and quinolones. Do not use in cows during lactation, whose milk is intended for human consumption. Do not use in pregnant animals and during lactation. Do not use in horses growing due to the risk of negative impact on the development of articular cartilage.

Adverse effects:
Enrofloxacin may cause damage to the articular cartilage during intense growth, especially in carnivorous animals of rapidly growing species. The injection site may cause local tissue reaction. Occasionally, gastrointestinal disorders may occur. There is a possibility of fluoroquinolones crystallized in acidic urine of carnivores. If you experience side effects after the administration of this product or notice any alarming symptoms not mentioned in the leaflet (including human symptoms due to contact with the drug), please inform the responsible veterinarian, responsible entity or the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products. The application form should be downloaded from the website http://www.urpl.gov.pl (Division of Veterinary Medicinal Products).

Target animal species:
Cattle (calves), pigs, dogs and cats.

Dosage for each species, route (s) and method of administration:
Subcutaneous or intramuscular administration. Repeated injections should be carried out in different places. Calves: The product should be administered subcutaneously. 5 mg enrofloxacin per kg of body weight, equivalent to 1 ml per 10 kg of body weight, given once a day, intramuscularly, for 3–5 days. Acute mycoplasma arthritis caused by enrofloxacin-sensitive Mycoplasma bovis bacteria: 5 mg enrofloxacin per kg of body weight, equivalent to 1 ml per 10 kg of body weight, administered once daily for 5 days. The product administered subcutaneously. Subcutaneous should not be given more than 10 ml of the product in one place. Pigs: 2,5 mg of enrofloxacin per kg of body weight, equivalent to 0,5 ml per 10 kg of body weight, administered once a day, intramuscularly, for three days. Infection of the digestive system or sepsis caused by Escherichia coli bacteria: 5 mg of enrofloxacin per kg of body weight, equivalent to 1 ml per 10 kg of body weight, administered once daily, intramuscularly, for 3 days. Injected in the neck, near the base of the ear. Once should not give more than 3 ml of the product. Cats and dogs: 5 mg of enrofloxacin per kg of body weight, equivalent to 1 ml per 10 kg of body weight, given once a day, subcutaneously, for a maximum of 5 days. Treatment can begin in the form of injectable product and continue in the form of tablets. The length of treatment should be determined based on the length of treatment for a given indication, defined in the product characteristics in the form of tablets.

Recommendations for correct administration:
Use according to the information provided in the information leaflet. To ensure correct dosage should be as precisely as possible to determine the body weight (bw). In order to avoid an underestimation of the dose.

Withdrawal period:
Calves: Subcutaneous use: Meat and offal: 12 days. The product is not approved for use in animals producing milk for human consumption. Pigs offal: 13 days.

Special precautions for storage:
Keep out of the sight and reach of children. Store at a temperature below 25°C. Protect from light. Do not use the veterinary medicinal product after the expiry date stated on the label. The expiry date is the last day of the month in question. Shelf life after first opening the container: 3 weeks.

Other information:
Pack size: 50 ml, 100 ml.

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