Entericolix, Emulsion for Injection for Pig
Active ingredients: Clostridium perfringens, Escherichia coli
Form
Injection
Species
Manufacturer
CZ Vaccines S.A.U.
VMD MA No.
30824/4003
What it's used for
expressing F4ac, F5, F6, F18ac and F41 adhesins, against oedema disease caused by E. coli strain expressing F18ab adhesin and against necrotic enteritis ca...
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Prescription required
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Entericolix, Emulsion for Injection for Pig — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
by E. coli strain expressing F18ab adhesin and against necrotic enteritis caused by
C. perfringens
Neonatal piglets
- The vaccine reduces mortality and clinical signs (severe diarrhoea) due to
colibacillosis.
- The vaccine reduces mortality and clinical signs due to necrotic enteritis caused
by C. perfringens
Weaned piglets
- The vaccine reduces mortality and clinical signs due to oedema disease.
- The vaccine reduces clinical signs (severe diarrhoea) of colibacillosis.
- The vaccine reduces clinical signs of chronic enteritis due to C. perfringens
C.
Duration of immunity:
- 21 days for infections caused by F4ac, F18ac, (colibacillosis) and C. perfringens
type C (necrotic enteritis).
- 21 days for antibodies against F5, F6 and F41, however the protective efficacy
of the antibody levels was not established.
- 28 days for infections caused by F18ab (oedema disease).
Avoid introduction of contamination during use.
Doses
Sows and gilts: 2 ml.
Before use, allow the vaccine to reach room temperature and shake the bottle
vigorously. Inoculate the corresponding dose by deep intramuscular injection in the
neck muscles. It is very important to use needles of appropriate length according to
the weight of the animal.
It is recommended that the second dose should be given preferably on the alternate
side.
Vaccination schedule
Pregnant sows: The initial course consists of two doses. Administer one dose
7 weeks before farrowing followed by a second dose 4 weeks before farrowing.
Revaccinate with a single dose 4 weeks before farrowing in subsequent gestation
periods.
to any of the excipients.
Very common
(>1 animal / 10 animals treated):
Hyperthermia1
Common
(1 to 10 animals / 100 animals treated):
Apathy
Rare
(1 to 10 animals / 10,000 animals treated):
Injection site swelling, injection site
reddening
Very rare
(<1 animal / 10,000 animals treated,
including isolated reports):
Anaphylactic-type reaction
1
Transient, maximum 2 ºC, between 4 – 24 hours after vaccination. Temperatures
return to normal values within 24 – 48 hours.
Between 1- and 2-days post-vaccination, uncommonly may last for up to 7 days
after vaccination.
With a maximum diameter of 3 cm and a maximum of 10 days of duration.
May be fatal.
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.
AN: 01156/2024 & 01571/2024Page 4 of 6
Special precautions for safe use in the target species:
Not applicable.
AN: 01156/2024 & 01571/2024Page 3 of 6
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.
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.
Do not freeze.
Protect from light.
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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Other Products Containing Clostridium perfringens
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Bravoxin Suspension for Injection for Cattle and Sheep
POM-VPSIntervet International B.V.
Bravoxin Suspension for Injection for Cattle and Sheep
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Covexin 10 Suspension for Injection for Sheep and Cattle
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Covexin 10 Suspension for Injection for Sheep and Cattle
POM-VPSZoetis Belgium S.A.
Enteroporc COLI AC Lyophilisate and Suspension for Suspension for Injection for Pigs
POM-VCeva Sante Animale
Enteroporc COLI AC Lyophilisate and Suspension for Suspension for Injection for Pigs
POM-VCeva Animal Health Ltd
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