Bovilis Bovipast RSP Vaccine for cattle 50ml (10 Dose)

raindication. Failure to vaccinate individual animals may promote the transmission of pathogens and development of disease. The magnitude of the antibody response may be reduced by maternally derived antibodies in calves up to six weeks of age. However, according to the results of challenge experiments, significant protection against infection by Bovine Respiratory Syncytial virus is still provided three weeks after the basic vaccination course, and significant protection against Parainfluenza-3 virus and Mannheimia haemolytica serotype A1 is still provided six weeks after the basic vaccination course. The results of challenge experiments in calves with maternally derived antibodies further indicate that the onset of cross-protective immunity to the A6 serotype is 2 weeks after completion of the vaccination course. Cross protective immunity is provided up to six weeks after the basic vaccination course as demonstrated by serological tests. Respiratory infections in calves are often associated with poor hygiene. Thus, general improvements in hygiene are important to support the effect of vaccination. Operator Warning In case of accidental self-injection seek medical advice immediately and show the package leaflet or the label to the physician. Adverse reactions In laboratory and field trials: Immunisation may commonly result in temporary swellings at the injection site (in extreme cases narrow swellings up to 10 cm long may occur). Typically, these swellings completely disappear or reduce in size to a negligible small lump within 2 to 3 weeks after vaccination, though in individual animals very small reactions can be found for up to 3 months. Additionally, a transient slight rise in body temperature, lasting a maximum of 3 days, may commonly occur after vaccination and at the same time a slight reluctance to move may be found. In very rare cases hypersensitivity reactions may occur. In post marketing experience: In very rare cases hypersensitivity reactions, which may be fatal, can occur. The frequency of adverse reactions is defined using the following convention: - very common (more than 1 in 10 animals treated displaying adverse reaction(s)) - common (more than 1 but less than 10 animals in 100 animals treated) - uncommon (more than 1 but less than 10 animals in 1,000 animals treated) - rare (more than 1 but less than 10 animals in 10,000 animals treated) - very rare (less than 1 animal in 10,000 animals treated, including isolated reports). Use during pregnancy or lactation Can be used during pregnancy and lactation. Interactions Safety and efficacy data are available which demonstrate that this vaccine can be administered on the same day but not mixed with MSD Animal Health’s live IBR marker vaccine (where this product is authorised) in cattle from 3 weeks of age onwards. No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product except the product mentioned above. 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. Immunosuppressive drugs should generally not be used directly before or after vaccination, since a satisfactory immune response will only be obtained in immuno-competent animals.
Vat Rate: 20%