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POM-V Prescription Required

MS-H Vaccine Oculonasal Suspension

Active ingredient: Mycoplasma synoviae

Form

Suspension

Species

Chickens

Manufacturer

Pharmsure Veterinary Products Europe Limited

VMD MA No.

61467/5000

What it's used for

For active immunisation of future broiler breeder chickens, future layer breeder chickens and future layer chickens from 5 weeks of age to reduce air sac l...

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

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Paying less for Mycoplasma synoviae

  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

MS-H Vaccine Oculonasal Suspension — SPC Details

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

For active immunisation of future broiler breeder chickens, future layer breeder
chickens and future layer chickens from 5 weeks of age to reduce air sac lesions and
reduce the number of eggs with abnormal shell formation caused by Mycoplasma
synoviae.
Onset of immunity: 4 weeks after vaccination.
Duration of immunity to reduce air sac lesions: 40 weeks post vaccination.
Duration of immunity to reduce the number of eggs with abnormal shell formation:
has not been established.
None.
See also section 4.7.

Revised: December 2025
AN: 02593/2025
Chickens:
None known.
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
contact details.
Do not use antibiotics with anti-Mycoplasma activity 2 weeks before or 4 weeks after
vaccination. Such antibiotics include e.g. tetracycline, tiamulin, tylosin, quinolones,
lincospectin, gentamicin or macrolide antibiotics.
Where antibiotics must be used, preference should be given to agents with no
antimycoplasma activity, such as penicillin, amoxicillin or neomycin. They should not
be given within 2 weeks after vaccination.
Vaccinate healthy animals only.

Special precautions for use in animals
All birds in a flock/common housed group must be vaccinated at the same time.
Only flocks with no antibodies to M. synoviae
should be carried out on -free birds at least 4 weeks before expected
exposure to virulent M. synoviae.
Pullets should first be tested for M. synoviae infection. Testing for the presence of
synoviae in the flock is normally by way of an indirect diagnostic assay (e.g. the rapid
serum agglutination test (RSAT) or ELISA) with blood samples being tested within 24
hours of collection. Testing by a direct diagnostic assay (e.g. PCR) for the presence
of M. synoviae is preferable due to the time required for seroconversion after
infection.
The vaccine strain can spread from vaccinated to unvaccinated birds, including wild
species. This may occur during the whole life of the vaccinated bird. Special
precautions should be taken to avoid spreading of the vaccine strain to other bird
species, and it is essential that all birds in the flock/common housed group are
vaccinated.
The vaccine strain can be detected in respiratory tract of the chickens until 55 weeks
after vaccination.
Distinguishing between field strains and the vaccine strain of M. synoviae can be
performed by Hammond classification or High Resolution Melt (HRM) testing by a
laboratory.
Infection with M. synoviae induces a transient positive antibody response to
Mycoplasma gallisepticum. Although no data are available on the matter, it is likely
that vaccination with this product will also induce a positive antibody response to
Mycoplasma gallisepticum and may therefore interfere with the serological monitoring
of Mycoplasma gallisepticum. If necessary, further differentiation of the 2
Mycoplasma species can be done by using PCR in a laboratory. Samples that can be
used for PCR include swabs taken from pathological sites such as trachea, palatine
cleft, air sacs or joints.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Personal protective equipment consisting of gloves and safety glasses should be
worn when handling the veterinary medicinal product.

Revised: December 2025
AN: 02593/2025
If vaccine is accidentally splashed into the operator’s eyes, the eyes and face should
be thoroughly washed with water to avoid any potential reaction to culture medium
constituents.
Special precautions for the protection of the environment
Not applicable.
Other precautions
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 frozen below -70 °C for a maximum of 5 years.
After removal from the deep freeze, further short-term storage is allowed at or below -
18 °C for no more than 4 weeks. Vaccine should not be stored back in -70 °C after
storage at or below -18 °C.
Protect from direct sunlight.

Revised: December 2025
AN: 02593/2025
CCU*
* colour changing units
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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