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POM-V Prescription Required

ProteqFlu Suspension for Injection for Horses

Active ingredient: Equine influenza virus

Form

Injection

Species

Horses

Manufacturer

Boehringer Ingelheim Vetmedica GmbH

VMD MA No.

04491/5047

What it's used for

Active immunisation of horses of 4 months of age or older against equine influenza to reduce clinical signs and virus excretion after infection. Onset of i...

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

The prescription itself has a price. See what practices near you charge for a consultation and the written prescription fee.

Paying less for Equine influenza virus

  1. 1

    Ask your vet for a written prescription

    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  2. 2

    Fill it at a registered online retailer

    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

ProteqFlu Suspension for Injection for Horses — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

Active immunisation of horses of 4 months of age or older against equine influenza
to reduce clinical signs and virus excretion after infection.
Onset of immunity: 2 weeks after primary vaccination course.
Duration of immunity induced by the vaccination scheme: 5 months after primary
vaccination course and 1 year after the third vaccination.

Issued: April 2023
AN: 00908/2022
None
Horses:
Rare
(1 to 10 animals / 10,000 animals
treated):
Injection site swelling
, increased skin
temperature, muscle stiffness, injection
site pain

Elevated temperature
Very rare
(<1 animal / 10,000 animals treated,
including isolated reports):
Injection site abscess
Apathy, decreased appetite
Hypersensitivity reaction
1
transient, usually regresses within 4 days; in rare occasions, swelling can reach a
diameter up to 15–20 cm, with duration up to 2–3 weeks that may require
symptomatic treatment.
max. 1.5 °C, for 1 day, exceptionally 2 days.
the day after vaccination.
which may require appropriate symptomatic treatment.
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 also the last section of
the package leaflet for respective contact details.

Issued: April 2023
AN: 00908/2022
Vaccinate healthy animals only.

Special precautions for use in animals:
Not applicable.
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.
Special precautions for the protection of the environment:
Not applicable.
Safety and efficacy data are available which demonstrate that this vaccine can be
administered on the same day but not mixed with Boehringer Ingelheim’s inactivated
vaccine against rabies.
The vaccines should be given at different sites.
Store and transport refrigerated (2 °C - 8 °C).
Do not freeze.
Protect from light.

Issued: April 2023
AN: 00908/2022
log10 FAID50*
* vCP content checked by global FAID50 (fluorescent assay infectious dose 50%) and
qPCR ratio between vCP.
Adjuvant:
Carbomer........................................................................................4 mg
Excipients:
For the full list of excipients, see section

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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