Composition:

each 8 gr. The syringe contains cephalexin monohydrate equivalent to 200 mg. of cephalexin and kanamycin monosulfate, which is equivalent to 100,000 IU kanamycin.

Target animals:

Lactating cows.

Pharmacotherapeutic group:

Antibacterial combined intracisternal preparations.

ATC vet code:

QJ51RD01

Indications:

Treatment of clinical mastitis in lactating cows caused by bacteria susceptible to the combination of cephalexin and kanamycin, such as Staphylococcus aureus, Streptococcus dysgalactiae,

Streptococcus uberis, Escherichia coli

Route of administration and dosage:

For intramammary use.
The contents of one syringe should be injected into each infected sore at an interval of 24 hours.

Before infusion, the wax should be completely drained, the mammary gland should be disinfected to avoid contamination of the syringe head.

Specific clinical information and special warnings for target animals:

The product should only be used to treat clinical mastitis. Product use should be based on bacterial susceptibility testing. If this is not possible, therapy should be based on regional and farm epidemiological information on the target bacterial species, as well as official national antimicrobial policies. Inappropriate use of the product may increase the spread of strains resistant to cephalexin and kanamycin and may reduce the effectiveness of treatment with other cephalosporins or aminoglycosides due to cross-resistance.

Use during pregnancy or lactation:

Laboratory studies on animals have not revealed any evidence of teratogenic effects. Studies in lactating animals have not revealed teratogenic or fetotoxic effects. It can be used in dairy cows.

Side effects:

does not have

Interaction with other drugs:

Should not be used together with bacteriostatic antibacterial agents. In case of resistance to cephalexin, cross-resistance to other cephalosporins is possible. In the case of resistance to kanamycin, cross-resistance between kanamycin, neomycin and paromomycin occurs. Unilateral resistance to streptomycin is also known.

Overdose symptoms and antidote:

Not used.

Waiting period:

Meat: 10 days, milk: 5 days

Contraindications:

Do not use in cows hypersensitive to kanamycin and/or cephalexin. Do not use in animals that are not lactating. Do not use in case of resistance to any of the active substances.

General warnings:

Consult a veterinarian before use and in case of unexpected effects.

Keep out of reach of children and away from foodstuffs.

Read the instructions before use.

Special precautions for persons who are directly involved in the process of treatment with the mentioned medical product:

People with hypersensitivity to cephalexin or kanamycin should avoid contact with the product. Cephalosporins can cause hypersensitivity reactions (allergy) after injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillin can cause a cross-allergic reaction to cephalosporins and vice versa. Allergic reactions caused by these substances can take a serious form. Do not touch the product if you are sensitive or if you have been advised not to work with such preparations. Exercise extreme caution when using the product to avoid exposure. Follow all recommendations.

If you develop a skin rash after exposure, consult your doctor for medical advice and show these instructions. Swelling of the face, lips or eyes or difficulty breathing are more serious symptoms and require immediate medical attention.

Storage conditions and validity period:

Store in factory packaging in a refrigerator below 25°C, do not freeze. The shelf life of the marketed veterinary drug is 2 years. Each syringe is for single use only.

Special precautions for the disposal of unused veterinary medicinal products or waste products derived from the use of such products

Any unused product or waste material should be disposed of in accordance with good pharmaceutical waste disposal practices and national regulations for waste disposal.

Commercial packaging:

White 8 g low-density polyethylene intracisternal syringe (plunger-tip) in a polypropylene container 48 and 120 pcs.

Marketing Authorization Holder:

Bavet İlaç San. ve Tic. A.Ş. Istanbul Tuzla Organize Sanayi

Bolgesi 12. Cad. No:8 34959 Tepeoren, Tuzla/Istanbul-Turkey

Manufacturer:

Arion Ilac San. Tic. A.S Istanbul Tuzla Organize Sanayi Bolgesi

12. Cad. No:8 34959 Tepeoren, Tuzla/Istanbul-Turkey

Importer in Georgia:

Invet Ltd. 404387481, Georgia, Tbilisi, 0154, Vakhushti Bagrationi st. N84a (032) 2 25 19 66