Coxevac Suspension for Injection for Cattle, Goats and Sheep
Active ingredient: Coxiella burnetii
Form
Injection
Species
Manufacturer
Ceva Animal Health Ltd
VMD MA No.
15052/5000
What it's used for
Cattle: For the active immunisation of cattle to lower the risk for non-infected animals vaccinated when nonpregnant to become shedder (5 times lower proba...
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Coxevac Suspension for Injection for Cattle, Goats and Sheep — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
For the active immunisation of cattle to lower the risk for non-infected animals
vaccinated when nonpregnant to become shedder (5 times lower probability in
comparison with animals receiving a placebo), and to reduce shedding of Coxiella
burnetii in these animals via milk and vaginal mucus.
Onset of immunity: not established.
Duration of immunity: 280 days after completion of the primary vaccination course.
Goats:
Revised: December 2024
AN: 02877/2023
Page 2 of 7For the active immunisation of goats to reduce abortion caused by Coxiella burnetii
and to reduce shedding of the organism via milk, vaginal mucus, faeces and
placenta.
Onset of immunity: not established.
Duration of immunity: one year after completion of the primary vaccination course.
Sheep:
For the active immunisation of sheep against Coxiella burnetii to reduce shedding of
the organism via milk, vaginal mucus and faeces.
Onset of immunity: not established
Duration of immunity: 4 months
AN: 02877/2023
Cattle:
Very common
(>1 animal / 10 animals
treated):
Injection site swelling* Rare
(1 to 10 animals / 10,000
animals treated):
Lethargy, Hyperthermia, Anorexia
* Palpable, of 9 to 10 cm diameter maximum, which may last for 17 days, reduces
gradually and disappears without need for treatment.
Goats:
Very common
(>1 animal / 10 animals
treated):
Injection site swelling*
Hyperthermia**
Uncommon
(1 to 10 animals / 1,000
animals treated):
Lethargy, Malaise, AnorexiaRare
(1 to 10 animals / 10,000
animals treated):
Diarrhoea
* Palpable, of 3 to 4 cm diameter maximum, which may last for 14 days, reduces and
disappears without need for treatment.
** For 4 days post-vaccination.
Sheep:
Very common
(>1 animal / 10 animals
treated):
Injection site inflammation, application site
thickening*
Rare
(1 to 10 animals / 10,000
animals treated)
Lethargy, Hyperthermia**, Anorexia
* Palpable, of 5 cm diameter maximum, which may last for 14 days, reduces and
disappears without need for treatment. Reactions are expected to be more severe
after the second injection.
** 2.5°C increase maximum, not lasting more than one day.
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 section 16 of the package leaflet for contact
details.
adverse effect.
No efficacy data are available concerning the use of COXEVAC in male animals.
However, in safety laboratory trials, the use of COXEVAC in males proved to be safe.
In the case that it is decided to vaccinate the whole herd, it is advisable to vaccinate
the male animals at the same time.
There are no benefits of the vaccine (as described in the indications for cattle), when
used in infected and/or pregnant cows.
The biological significance of the levels of reduction shown in shedding in cattle and
goats is not known.
i) Special precautions for use in animals
It is advisable to vaccinate all the animals in the herd at the same time.
Under field conditions, vaccination with COXEVAC has commonly been followed by a
decrease in milk production in goats. Since stress could contribute to this adverse
reaction, appropriate precautions should be taken to reduce stress as much as
possible during the administration of the product.
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.
iii) Other precautions
None
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.
Keep the vial in the outer carton in order to protect from light.
5. IMMUNOLOGICAL PROPERTIES
Pharmacotherapeutic group: immunologicals for bovidae, inactivated bacterial
vaccines for cattle.
ATC Vet Code: QI02AB.
The vaccine contains phase I Coxiella burne
immunity against Q fever in cattle, goats and sheep.
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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Other Products Containing Coxiella burnetii
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
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