Other products
Porcilis Ery+Parvo vet.
Active substance
ATC code
Species
Pigs (sows and gilts).
Indications
For the active immunisation of sows and gilts to prevent clinical signs of Erysipelas disease caused by all relevant Erysipelothrix rhusiopathiae serotypes (serotype 1 and 2), and for protection against embryonal and foetal death caused by porcine parvovirus (PPV) infection.
E. rhusiopathiae:
Onset of immunity: 3 weeks.
Duration of immunity: 6 months.
Porcine parvovirus (PPV):
Duration of immunity: 12 months.
Dose to be administered and administration route
Intramuscular use.
Administer one dose of 2 ml by deep intramuscular injection behind the ear.
Before use, allow the vaccine to reach room temperature. Shake well before and regularly during use.
Use sterile vaccination equipment. Avoid introduction of contamination by multiple broaching.
Primary vaccination course:
Protection against E. rhusiopathiae and PPV should be achieved in gilts before first mating.
To induce protection against erysipelas, a double vaccination as a primary vaccination course is advised. This can be achieved with the monovalent erysipelas vaccine (Porcilis Ery) either 4 weeks before or 4 weeks after use of this combined erysipelas and PPV vaccine.
A single injection not later than 2 weeks before mating is sufficient to protect the following pregnancy from damage due to PPV.
To avoid possible interference from maternal antibodies the pigs should be 6 months old before vaccination to ensure efficacy against PPV.
Revaccination:
Revaccinations should be administered once a year, supplemented with the administration of the monovalent erysipelas vaccine (Porcilis Ery), 6 months after use of this combined erysipelas and PPV vaccine.
Adverse reactions
Pigs (sows and gilts):
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Very common (> 1 animal / 10 animals treated): |
|
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Common (1 to 10 animals / 100 animals treated): |
Reluctant to move3. |
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Very rare (< 1 animal / 10 000 animals treated, including isolated reports): |
Hypersensitivity reaction. |
1 Transient increase (+ 0.5 °C) within 24 hours after vaccination.
2 Mild transient local swelling (1 – 10 mm diameter) until 8 days after vaccination.
3 Transient reaction.
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 respective contact details.
Dispensing
POM-V - Prescription Only Medicine – Veterinarian
TRUSTED SOURCE
SUMMARY OF PRODUCT CHARACTERISTICS
1. NAME OF THE VETERINARY MEDICINAL PRODUCT
Porcilis Ery+Parvo suspension for injection for pigs
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 2 ml dose contains:
Active substances:
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Erysipelothrix rhusiopathiae, serotype 2, strain M2, inactivated: |
≥ 1 ppd* |
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Porcine parvovirus, strain 014, inactivated: |
≥ 552 EU** |
* ppd = pig protective dose as compared to a reference preparation known to be protective in pigs.
** EU = as determined in the final product by antigenic mass ELISA.
Adjuvant:
dl-α-tocopherol: 150 mg Excipients:
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Qualitative composition of excipients and other constituents |
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Polysorbate 80 |
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Tris (hydroxymethyl) aminomethane |
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Sodium chloride |
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Simethicone |
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Hydrochloric acid |
|
Water for injections |
Homogenous white to nearly white suspension after shaking.
3. CLINICAL INFORMATION
3.1 Target species
Pigs (sows and gilts).
3.2 Indications for use for each target species
For the active immunisation of sows and gilts to prevent clinical signs of Erysipelas disease caused by all relevant Erysipelothrix rhusiopathiae serotypes (serotype 1 and 2), and for protection against embryonal and foetal death caused by porcine parvovirus (PPV) infection.
E. rhusiopathiae:
Onset of immunity: 3 weeks.
Duration of immunity: 6 months.
Porcine parvovirus (PPV):
Duration of immunity: 12 months.
3.3 Contraindications None.
3.4 Special warnings
Vaccinate healthy animals only.
3.5 Special precautions for use
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:
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.
3.6 Adverse events
Pigs (sows and gilts):
|
Very common (> 1 animal / 10 animals treated): |
|
|
Common (1 to 10 animals / 100 animals treated): |
Reluctant to move3. |
|
Very rare (< 1 animal / 10 000 animals treated, including isolated reports): |
Hypersensitivity reaction. |
3.7 Use during pregnancy, lactation or lay
Pregnancy and lactation:
Can be used during pregnancy and lactation.
3.8 Interaction with other medicinal products and other forms of interaction
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.
3.9 Administration routes and dosage
Intramuscular use.
Administer one dose of 2 ml by deep intramuscular injection behind the ear.
Before use, allow the vaccine to reach room temperature. Shake well before and regularly during use.
Use sterile vaccination equipment. Avoid introduction of contamination by multiple broaching.
Primary vaccination course:
Protection against E. rhusiopathiae and PPV should be achieved in gilts before first mating.
To induce protection against erysipelas, a double vaccination as a primary vaccination course is advised. This can be achieved with the monovalent erysipelas vaccine (Porcilis Ery) either 4 weeks before or 4 weeks after use of this combined erysipelas and PPV vaccine.
A single injection not later than 2 weeks before mating is sufficient to protect the following pregnancy from damage due to PPV.
To avoid possible interference from maternal antibodies the pigs should be 6 months old before vaccination to ensure efficacy against PPV.
Revaccination:
Revaccinations should be administered once a year, supplemented with the administration of the monovalent erysipelas vaccine (Porcilis Ery), 6 months after use of this combined erysipelas and PPV vaccine.
3.10 Symptoms of overdose (and where applicable, emergency procedures and antidotes)
Reactions observed after administration of a two-fold overdose are not different from those observed after administration of a single dose.
3.11 Special restrictions for use and special conditions for use, including restrictions on the use of antimicrobial and antiparasitic veterinary medicinal products in order to limit the risk of development of resistance
Not applicable.
3.12 Withdrawal periods Zero days.
4. IMMUNOLOGICAL INFORMATION
4.1 ATCvet code: QI09AL01.
The active substances are a lysate of E. rhusiopathiae strain M2 (serotype 2) and inactivated porcine parvo virus strain 014.
For the active immunisation of sows and gilts, as an aid in the control of swine erysipelas and for the protection of their embryos and foetuses against porcine parvovirus infection.
The antigens are incorporated in an aqueous tocopherol-based adjuvant in order to enhance a prolonged stimulation of immunity.
5. PHARMACEUTICAL PARTICULARS
5.1 Major incompatibilities
Do not mix with any other veterinary medicinal product.
5.2 Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years. Shelf life after first opening the immediate packaging: 10 hours.
5.3 Special precautions for storage
Store in a refrigerator (2 °C – 8 °C).
Do not freeze.
Protect from light.
5.4 Nature and composition of immediate packaging
PET (polyethylene terephthalate) vial closed with a halogenobutyl rubber stopper and sealed with a coded aluminium cap.
Pack sizes:
Cardboard box containing 1 vial of 20 ml (10 doses), 50 ml (25 doses), 100 ml (50 doses) or 250 ml (125 doses).
Not all pack sizes may be marketed.
5.5 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products
Medicines should not be disposed of via wastewater or household waste.
Use take-back schemes for the disposal of any unused veterinary medicinal product or waste materials derived thereof in accordance with local requirements and with any national collection systems applicable to the veterinary medicinal product concerned.
6. NAME OF THE MARKETING AUTHORISATION HOLDER
Intervet International B.V.
7. MARKETING AUTHORISATION NUMBER
Vm 06376/5052
8. DATE OF FIRST AUTHORISATION
16 July 1997
9. DATE OF THE LAST REVISION OF THE SUMMARY OF THE PRODUCT CHARACTERISTICS
February 2026
10. CLASSIFICATION OF VETERINARY MEDICINAL PRODUCT
Veterinary medicinal product subject to prescription.
Find more product information by searching for the ‘Product Information Database’ on www.gov.uk.
Gavin Hall Approved: 17 February 2026
[1] Transient increase (+ 0.5 °C) within 24 hours after vaccination.
[2] Mild transient local swelling (1 – 10 mm diameter) until 8 days after vaccination. 3 Transient reaction.
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 respective contact details.
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