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POM-V Prescription Required

Bovela Lyophilisate and Solvent for Suspension for Injection for Cattle

Active ingredient: Bovine viral diarrhoea virus

Form

Injection

Species

Cattle

Manufacturer

Boehringer Ingelheim Vetmedica GmbH

VMD MA No.

EU/2/14/176/001-016

What it's used for

For active immunisation of cattle from 3 months of age to reduce hyperthermia and to minimise the reduction of leukocyte count caused by bovine viral diarr...

Full indications, dosage and side effects ↓
View official SPC (PDF)

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Prescription required

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Clinical information

Bovela Lyophilisate and Solvent for Suspension for Injection for Cattle — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

For active immunisation of cattle from 3 months of age to reduce hyperthermia and
to minimise the reduction of leukocyte count caused by bovine viral diarrhoea virus
(BVDV-1 and BVDV-2), and to reduce virus shedding and viraemia caused by
BVDV-2.
For active immunisation of cattle against BVDV-1 and BVDV-2, to prevent the birth of
persistently infected calves caused by transplacental infection.
Onset of immunity: 3 weeks after immunisation.
Duration of immunity: 1 year after immunisation.

Amended pages: March 2026
AN: 04071/2024
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
Target species: cattle
Common
(1 to 10 animals / 100 animals
treated):
Elevated temperature* Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):

Injection site swelling or
Injection site nodule**
Hypersensitivity reaction including anaphylactic-
type reaction.
*within the physiological range is common within 4 hours of vaccination, resolving
within 24 hours**≤ 3 cm in diameter, resolving within 4 days after vaccination
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 the national competent authority via
the national reporting system. See also the last section of the package leaflet for
respective contact details.
Long lasting viremia has been observed after vaccination, in particular in pregnant
seronegative heifers (10 days in a study). This may result in transplacental
transmission of the vaccine virus, but no adverse effects on foetus or pregnancy was
observed in studies.
Shedding of the vaccine virus by body fluids cannot be excluded.
The vaccine strains are able to infect sheep and swine when administered
intranasally, but no adverse reactions or spreading to in-contact animals has been
demonstrated.
The vaccine has not been tested in breeding bulls and should therefore not be used
in breeding bulls.

i) Special precautions for use in animals
Vaccinate healthy animals only.
To ensure the protection of animals introduced to the herd where BVDV is
circulating, vaccination has to be completed 3 weeks before introduction.
The cornerstone of bovine viral diarrhoea (BVD)-eradication is identification and
culling of persistently infected animals. A definitive diagnosis of persistent infection
can only be established upon re-testing in blood after an interval of at least 3 weeks.
In some limited cases with newborn calves, positive ear notches for BVDV vaccine
strain were reported by molecular diagnostic tests. Additional laboratory tests to
differentiate vaccine strain virus from field strain are available upon request from the
marketing authorisation holder.
The field studies to investigate the efficacy of the vaccine were done in herds where
persistently infected animals had been removed.
ii) Special precautions to be taken by the person administering the veterinary
medicinal product to animals
In case of accidental self-injection, seek medical advice immediately and show the
package leaflet or the label to the physician.

Amended pages: March 2026
AN: 04071/2024
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.
Store and transport refrigerated (2 °C – 8 °C).
Do not freeze.
Keep the lyophilisate and the solvent vials in the outer carton.
Zero days.
5. IMMUNOLOGICAL PROPERTIES
Pharmacotherapeutic group: Immunologicals for bovidae, live viral vaccines
ATC Vet Code: QI02AD02
The vaccine is designed to stimulate the development of an active immune response
against BVDV-1 and BVDV-2 in cattle.

Amended pages: March 2026
AN: 04071/2024

This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.

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