Country: Germany
Language: English
Source: HMA (Heads of Medicines Agencies)
trichophyton verrucosum 7000000 IU/ml
Intervet Deutschland GmbH
QI02AP01
Powder and solvent for suspension for injection
Trichophyton vaccine
Cattle Food
2008-03-11
June 2008 FEHLER! VERWEISQUELLE KONNTE NICHT GEFUNDEN WERDEN. BOVILIS® RINGVAC FEHLER! VERWEISQUELLE KONNTE NICHT GEFUNDEN WERDEN. I.B. SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE VETERINARY MEDICINAL PRODUCT Bovilis Ringvac, lyophilisate for suspension for injection, for cattle 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Per 1 ml of vaccine: ACTIVE SUBSTANCE: Attenuated _Trichophyton verrucosum,_ strain LTF-130 9 x 10 6 and 21 x 10 6 viable microconidia. EXCIPIENTS: For a full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Lyophilisate and solvent for suspension for injection. 4. CLINICAL PARTICULARS 4.1 TARGET SPECIES Cattle. 4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES Active immunisation of calves and cattle at risk of infection or calves and cattle suffering from dermatophytosis induced by _Trichophyton verrucosum_. The prophylactic vaccination reduces clinical signs of _Trichophyton verrucosum_ induced dermatophytosis while the therapeutic use results in a 2-fold faster recovery of animals which already show clinical signs of disease. Protective immunity is present within 3 weeks after vaccination and was shown to last for at least one year in a laboratory study. Field experience shows that if consequent herd immunisation is practised generally no revaccinations are required (cf. section 4.9). 4.3 CONTRAINDICATIONS Animals with fever and / or with dermatophytosis -independent symptoms of an infectious disease, as well as animals that are treated with corticosteroids, must be excluded from vaccination. 4.4 SPECIAL WARNINGS None. 4.5 SPECIAL PRECAUTIONS FOR USE Read the complete document