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POM-V Prescription Required

Porcilis M Hyo ID Once Emulsion for Injection for Pigs

Active ingredient: Mycoplasma hyopneumoniae

Form

Injection

Species

Pigs

Manufacturer

Intervet International B.V.

VMD MA No.

06376/3007

What it's used for

Duration of immunity: 22 weeks after vaccination.

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

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Paying less for Mycoplasma hyopneumoniae

  1. 1

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  2. 2

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    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

Porcilis M Hyo ID Once Emulsion for Injection for Pigs — SPC Details

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

Duration of immunity: 22 weeks after vaccination.
Intradermal administration of 0.2 ml per animal preferably at the sides of the neck or
along the muscles of the back using a multi-dose needle-free injection device for
intradermal application of liquids suitable to deliver a “jet-stream” volume of vaccine
(0.2 ml ± 10%) through the epidermal layers of the skin. A small, transient,
intradermal lump observed after the intradermal application is indicative of the
appropriate vaccination technique.
Safety and efficacy of Porcilis M Hyo ID ONCE have been demonstrated using the
device IDAL.
Vaccination scheme:
Vaccinate once from an age of 2 weeks onwards.
Before using the vaccine allow it to reach room temperature (15 - 25 
well before use.
Avoid introduction of contamination.
None.
Pigs:
Very common
(>1 animal / 10 animals
treated):
Elevated temperature
, injection site swelling
Uncommon
(1 to 10 animals / 1,000 animals
treated):
Lying down, malaise
A transient elevated temperature (mean 0.7 °C, in individual pigs up to 2 °C) very
commonly occurs on the day of vaccination. The animals return to normal 1 to 2 days
after the peak temperature is observed
A transient injection site swelling mostly consisting of hard non-painful button-like
swellings of a diameter of up to 4 cm can be very commonly observed. In individual
pigs redness and/or a biphasic pattern of the injection site swelling, consisting of an
increase and decrease followed by another increase and decrease of the size, may
be observed. The injection site swelling disappears completely within approximately 7
weeks 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 its local representative or the national
competent authority via the national reporting system. See also the package leaflet
for respective contact details.
Vaccinate healthy animals only.

Special precautions for safe use in the target species:
Not applicable.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
To the user:
This veterinary medicinal product contains mineral oil. Accidental injection/self-
injection may result in severe pain and swelling, particularly if injected into a joint or
finger, and in rare cases could result in the loss of the affected finger if prompt
medical attention is not given. If you are accidentally injected with this veterinary
medicinal product, seek prompt medical advice even if only a very small amount is
injected and take the package leaflet with you. If pain persists for more than 12 hours
after medical examination, seek medical advice again.
To the physician:
This veterinary medicinal product contains mineral oil. Even if small amounts have
been injected, accidental injection with this veterinary medicinal product can cause
intense swelling, which may, for example, result in ischaemic necrosis and even the
loss of a digit. Expert, PROMPT, surgical attention is required and may necessitate
early incision and irrigation of the injected area, especially where there is involvement
of finger pulp or tendon.
Special precautions for the protection of the environment:
Not applicable.
Safety and efficacy data are available in pigs from 3 weeks of age onwards which
demonstrate that this vaccine can be administered on the same day, but non-mixed
with Porcilis PRRS (intradermal route) and/or non-mixed with Porcilis PCV ID or with
Porcilis PCV ID mixed with Porcilis Lawsonia ID providing that non-mixed
administration sites of vaccines are separated by at least 3 cm. Adverse events are
as described in section 3.6, except for injection site swelling where a maximum size
of up to 6 cm may occur in individual pigs. Injection site swellings may last 8 weeks
and are very commonly accompanied by redness and crusts. In the event that the
crust is rubbed off, some small skin damage may be commonly observed.
The product information of Porcilis PCV ID, Porcilis Lawsonia ID and Porcilis PRRS
should be consulted before administration.
No information is available on the safety and efficacy of this vaccine when used with
any other veterinary medicinal product except the products mentioned above. 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 in a refrigerator (2 °C - 8 °C).
It has been demonstrated that transport at 30 °C for 3 days has no impact on the
quality of the product. Do not freeze.
Protect from direct sunlight.
Zero days.

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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