Expiration date: 01/2026
DESCRIPTION
Polyvak-TM vaccine against dermatomycosis in dogs. In appearance, it is a homogeneous liquid of light brown color with a thin sediment on the bottom, which disappears when shaken.
STRUCTURE
It includes 8 species and varieties of fungi from the genus Trichophyton and Microsporum.
PHARMACOLOGICAL PROPERTIES
Immunity in vaccinated animals occurs 20-30 days after the second vaccination and persists for at least 12 months from the first administration of the vaccine.
INDICATIONS
For preventive and therapeutic vaccination of dogs with dermatophytosis, the causative agents of which are fungi of the genera Trichophyton and Microsporum.
DOSAGE AND APPLICATION
Prophylactic and therapeutic purpose of the vaccine is administered intramuscularly in shinaberry muscles, neck, shoulder blade at the following doses: dogs aged 1-10 months – prophylactic — 0.3 ml; treatment — 0.5 ml; older than 10 months prophylaxis — 0.3 ml; medical — 0,6 ml. When using the vaccine for therapeutic purposes, double and triple administration of the vaccine is used at intervals of 10-14 days. The skin at the injection site is disinfected with 70 % ethyl alcohol or 0.5 % carbolic acid solution. Syringes and needles are sterilized by boiling before use, and a separate needle is used to vaccinate each animal. To accelerate the rejection of crusts, the affected areas of the skin are recommended to be treated with softening agents – fish oil, lanolin, vaseline, and other mineral or vegetable oils used in medicine and veterinary medicine. Before use, the vial or ampoule with the vaccine is shaken. Before applying the vaccine, all dog populations should be clinically examined. Given that the introduction of the vaccine to animals in the incubation period of the disease accelerates the clinical manifestation of dermatomycosis, it is necessary to carry out general vaccination in therapeutic doses in nurseries and other enterprises that are not affected by dermatomycosis. In weak, emaciated dogs with metabolic disorders and affected by ectoparasites, the preventive and therapeutic effectiveness of the vaccine is reduced. Regrouping and transportation of animals in dermatomycosis-free kennels and other enterprises is allowed without restrictions 14 days after vaccination. All newly received animals are vaccinated during their quarantine period. After the end of vaccinations, an act is drawn up indicating the date, the number of immunized animals, the epizootic state of the farm, the number of the vaccine series, the expiration date and date of manufacture, the manufacturer, as well as the persons who carried out the vaccination. The act also indicates the amount of biological product and disinfectant used for vaccination.
SPECIAL INSTRUCTIONS
No special precautions are provided.
CONTRAINDICATIONS
It is not allowed to vaccinate animals with high fever and patients with infectious diseases.
SIDE EFFECTS
When vaccinating healthy animals, no changes in the clinical condition are observed. In some individuals, there is a slight swelling and inflammation at the site of administration of the vaccine, which spontaneously disappears without medical intervention after 3-4 days. When vaccinating animals that are in the incubation period of the disease, vaccination accelerates the manifestation of the clinical picture of dermatomycosis with the appearance of multiple foci of a superficial nature. Animals that have shown clinical signs of the disease should be given a therapeutic dose of the vaccine, and in particularly severe cases, the vaccine should be administered 3-4 times. The interval between injections of the vaccine is 10-14 days.
SHELF LIFE AND STORAGE
In a dry place, out of the reach of children and animals, at a temperature of 2 to 10 ° C. The shelf life of the vaccine is 18 months from the date of manufacture, subject to storage conditions in the original packaging. In the absence of labeling, violation of the integrity of the vials, color changes, the presence of non-breaking flakes, foreign impurities, the vials with the vaccine are decontaminated by boiling for 15 minutes.
PACKAGING
They are produced in hermetically sealed vials or ampoules containing 1 dose (1 dose is 0.6 ml).
