Inactivated vaccine against dermatophytosis in bovine animals
Qualitative and quantitative composition of active substances
1 ml of the vaccine contains: Inactivated Trichophyton verrucosum 43 strain with a concentration of not less than 20%
Active immunization of cattle to reduce mortality and clinical signs of dermatophytosis caused by Trichophyton verrucosum infection.
Therapeutic use of the vaccine in animals with trichophytosis skin symptoms to accelerate the recovery process. Immunity appears 3-4 weeks after the second injection. The duration of immunity after 2 doses is 9-12 months.
Slight limited swelling may occur at the injection site, which resolves spontaneously within a few days.
About the occurrence of side effects after administering this product or observing any disturbing symptoms not mentioned in the leaflet (including symptoms in humans as a result of contact with the drug), please notify the competent veterinarian, the responsible entity or the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products. . The application form should be downloaded from the website https://www.urpl.gov.pl (Department of Veterinary Medicinal Products).
Dosage and route of administration
The vaccine should be used twice with an interval of 10-14 days.
Administer intramuscularly in the area of the gluteal muscles according to the following scheme:
Prophylactically from 1 week to 4 months of age – 5 ml
from 4 months to 8 months of age – 5 ml to 6 ml
over 8 months of age – 6 ml to 7 ml
Therapeutically from 1 week to 4 months of age – 7.5 ml
from 4 months to 8 months of age – 7.5 ml to 9 ml
over 8 months of age – 9 ml to 10.5 ml
The product can be used during pregnancy and lactation.
Recommendations for correct administration
Special precautions for storage and transport
Keep out of the reach and sight of children.
Store in a refrigerator (2-8oC). Do not freeze.
Use the contents of the opened immediate packaging within 14 days.
Do not use after the expiry date stated on the label.
Special warnings and precautions
In the event of accidental self-injection, immediately seek medical help and show the doctor the information leaflet or packaging.
No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product. A decision to use this vaccine before or after any other veterinary medicinal product therefore needs to be made on a case by case basis.
When administering a double dose, no side effects other than those stated in the section on adverse reactions were observed.
As no compatibility studies have been performed, this veterinary medicinal product must not be mixed with other veterinary medicinal products.
Special precautions concerning the disposal of unused veterinary medicinal product or waste derived from this product
Medicines should not be disposed of via wastewater or with household waste.
Ask your veterinarian about how to remove useless drugs. They will allow for better protection of the environment.
Period of validity
To be supplied on a prescription – Rp. To be administered under the supervision of a veterinarian. For animals only.
For information about this veterinary medicinal product, please contact the Marketing Authorization Holder.