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POM-V Prescription Required

Equip EHV1,4 Suspension for Injection

Active ingredients: Equid herpesvirus 1, Equid herpesvirus 4

Form

Injection

Species

Horses

Manufacturer

Zoetis Belgium S.A.

VMD MA No.

60021/3009

View official SPC (PDF)

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  1. 1

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  2. 2

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Prescription required

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Clinical information

Equip EHV1,4 Suspension for Injection — SPC Details

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

Primary course:
a second injection after an interval of 4 to 6 weeks.
In the event of increased infection risk, for example when a foal had consumed insufficient
colostrum or there is a risk of early exposure to field infections with EHV-1 or EHV-4,
earlier vaccination may be given. In these circumstances, the foal should receive a single
dose from 3 months of age followed by the above mentioned full primary vaccination
course.
Booster:
administered every 6 months.
Use in pregnant mares:
should be vaccinated during the 5
th
, 7
th
, and 9
th
month of pregnancy with a single 1.5 ml
dose on each occasion.
None.
Horses:
Very common
(>1 animal / 10 animals treated):
Injection site swelling
Common
(1 to 10 animals / 100 animals treated):
Elevated temperature
Rare
(1 to 10 animals / 10,000 animals treated):
Stiff gait
Anorexia, Lethargy
Very rare
(<1 animal / 10,000 animals treated, including
isolated reports):
Hypersensitivity reaction
1 Transient. Up to 5 cm in diameter, disappearing within a few to 6 days post vaccination.
2 Transient. Up to 2 days following dosing not exceeding 1.7°C.
3 Appropriate treatment is recommended / treat symptomatically.
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 the package leaflet for respective contact details.
Vaccinate healthy animals only.

Special precautions for safe use in the target species:
The vaccine may not be effective in animals incubating the disease at the time of
vaccination.
In the event of an allergic or anaphylactic reaction, immediate treatment should be given
with a soluble glucocorticoid intravenously (e.g. dexamethasone sodium phosphate),
adrenaline intramuscularly or antihistamine intramuscularly. Animals that have received
immunosuppressive drugs (e.g. glucocorticoids) should not be vaccinated until an interval
of at least 4 weeks has elapsed.
Syringes and needles should not have been sterilised chemically or be above ambient
temperature. Do not use chemicals to disinfect or sterilise the skin.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Not applicable.
Special precautions for the protection of the environment:
Not applicable.
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.
Store in the original package.
Protect from light.
Zero days.
4. IMMUNOLOGICAL INFORMATION
4.1 ATCvet code: QI05AA05
To stimulate active immunity against equine herpesvirus 1 and 4.
5.

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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