Bovalto Respi 3
Active substance
ATC code
Species
Cattle.
Indications
For active immunisation of cattle in the absence of maternally derived antibodies against:
- parainfluenza 3 virus, to reduce virus excretion due to infection,
- bovine respiratory syncytial virus, to reduce virus excretion due to infection,- Mannheimia haemolytica serotype A1, to reduce clinical signs and lung lesions.
Onset of immunity: 3 weeks.
Duration of immunity: 6 months.
Dose to be administered and administration route
Subcutaneous use.
Dose: 2 ml administered subcutaneously.
Warm before use to a temperature of 15 °C to 25 °C and shake the contents of the bottle.
Primary vaccination
Calves from non-immune dams: two doses three weeks apart from 2 weeks of age.
For calves from immune dams or where the immune status of the dam is unknown, the vaccination scheme should be adapted at the discretion of the veterinarian to take into account potential interference of maternally derived antibodies with the response to vaccination.
Revaccination
Administer one dose six months after completion of the primary vaccination scheme.
The efficacy of revaccination was demonstrated by measurement of the serological response and has not been assessed by challenge.
Adverse reactions
Cattle:
Very common (>1 animal / 10 animals treated): | Injection site swelling* |
Common (1 to 10 animals / 100 animals treated): | Hyperthermia** |
Very rare (<1 animal / 10,000 animals treated, including isolated reports): | Anaphylactic-type reactions*** Injection site pain**** |
* This swelling could reach up to 10 cm or more in diameter and may be associated with pain, and usually progressively reduces and disappears within 6 weeks after vaccination.
** Transient and slight, higher after the second injection (1.5 °C at most) lasting up to 3 days after vaccination.
*** Appropriate symptomatic treatment should be administered.
**** Associated with injection site swelling.
Reporting adverse events is important. It allows continuous safety monitoring of a veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to either the marketing authorisation holder or its local representative or the national competent authority via the national reporting system. See the package leaflet for respective contact details.
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|---|---|
| Art. Nr. | 08327/5010 |
| EAN | 3661103051190 |
