Heptavac P Plus Suspension for Injection for Sheep
Active ingredients: Clostridium chauvoei, Clostridium novyi, Clostridium perfringens, Clostridium septicum, Clostridium tetani, Mannheimia haemolytica, Pasteurella trehalosi
Form
Injection
Species
Manufacturer
Intervet International B.V.
VMD MA No.
06376/3020
What it's used for
Cl.chauvoei and Cl.tetani pneumonic pasteurellosis in sheep of all ages from a minimum age of 3 weeks and in the control of systemic pasteurellosis in wean...
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Heptavac P Plus Suspension for Injection for Sheep — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
pneumonic pasteurellosis in sheep of all ages from a minimum age of 3 weeks and in
the control of systemic pasteurellosis in weaned fattening and breeding sheep.
The vaccine may be used in pregnant ewes as an aid in the control of lamb
dysentery, pulpy kidney, tetanus and pasteurellosis in their lambs provided that the
lambs receive sufficient immune colostrum during the first 1-2 days of life.
Onset of immunity: As with most inactivated vaccines, significant levels of immunity
cannot be expected until 2 weeks after the second dose of vaccine in the primary
vaccination course.
Duration of immunity: Evidence of efficacy of the Pasteurella/Mannheimia component
of this vaccine was generated in an experimental infection model and it is not
possible to provide duration of immunity information using this system. There are
reports that active immunity will last for up to 1 year and that passive immunity will
persist for up to 4 weeks after birth in lambs from ewes vaccinated with conventional
Pasteurella vaccines.
through an area of clean, dry skin taking precautions against contamination. All
breeding sheep not previously vaccinated with this vaccine must receive two
injections, each of 2.0 ml, separated by an interval of 4-6 weeks. Thereafter they
must receive booster injections at intervals of not more than 12 months. In adult
breeding ewes these yearly booster injections should be given during the pre-
lambing period, 4-6 weeks pre-lambing, as an aid in control of disease in their lambs.
On farms where the incidence of pasteurellosis is high, a supplementary booster
injection using a Pasteurella vaccine may be required 2-3 weeks prior to expected
seasonal outbreaks.
This vaccine should not be used in lambs less than 3 weeks of age due to the
possible immunological incompetence of the very young lamb and competition from
any maternally derived colostral antibodies. Lambs being retained for fattening or
subsequent breeding will require a full course of vaccination. At a minimum age of 3
weeks these lambs should receive two injections, each of 2.0 ml, separated by an
interval of 4-6 weeks. It should be noted that this vaccine is the recommended
vaccine for breeding stock since it provides optimal aid in the control of the
predominant clostridial diseases in adult sheep by active immunisation and in young
lambs by passive immunisation.
The vaccine bottle must be shaken well before use. The use of automatic vaccination
equipment is recommended. Since the bottle is non-collapsible, a vaccinator with a
vented draw-off spike or similar device must be used. The instructions supplied with
such equipment should be noted and care should be taken to ensure the delivery of
the full dose, particularly with the final few doses from the bottle. Strict precautions
should be taken against contamination of the vaccine. A fresh sterile needle must be
used each time the rubber cap is punctured, to avoid contamination of the remaining
contents. Syringes and needles must be from gamma irradiated packs or freshly
sterilised by boiling for at least 20 minutes.
This vaccine has been developed following research and development which
resulted in the application of Plus ‘IRP’ technology for the manufacture of the
Pasteurella/Mannheimia components of this vaccine. The inclusion of these IRP
components should provide enhanced efficacy and cross protection e.g. protection
against serotype A12, which is not included in the vaccine, has been demonstrated.
Studies on the response of sheep to this vaccine show that two injections separated
by an interval of 4-6 weeks are required to gain the full benefit of the ‘IRP’.
Common
(1 to 10 animals / 100 animals treated):
Injection site reaction
.Very rare
(<1 animal / 10,000 animals treated,
including isolated reports):
Hypersensitivity reaction,
anaphylaxis
.
Small and transient. Usually characterised by swelling. May be present for up
to 3-4 months post-vaccination.
Sometimes fatal. If such reaction occurs, appropriate treatment should be
administered without delay.
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.
Special precautions for safe use in the target species:
This vaccine should not be used in lambs less than 3 weeks of age. The nutritional
and metabolic status of pregnant ewes is extremely important at the time of
vaccination. If in doubt, advice should be sought from a veterinary surgeon.
In any group of animals, a small number of individuals may fail to respond to
vaccination as a result of immunological incompetence. Satisfactory immune
responses will only be attained in healthy animals, thus it is important to avoid
vaccination of animals which have intercurrent infection or metabolic disorder.
When handling sheep, stress should be avoided, particularly during the later stages
of pregnancy when there is a risk of inducing abortion and metabolic disorders.
Because sheep are very sensitive to contamination of the injection site (which may
result in non-product related tissue reactions and even in abscesses), it is advised to
follow strict aseptic injection techniques.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Accidental self-injection might result in localized swelling, severe pain, soft tissue
injury or infection. 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.
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 chauvoei
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Blackleg Vaccine
POM-VPSZoetis Belgium S.A.
Blackleg Vaccine
POM-VPSZoetis UK Limited
Bravoxin Suspension for Injection for Cattle and Sheep
POM-VPSIntervet International B.V.
Bravoxin Suspension for Injection for Cattle and Sheep
POM-VPSIntervet International B.V.
Covexin 10 Suspension for Injection for Sheep and Cattle
POM-VPSZoetis UK Limited
Covexin 10 Suspension for Injection for Sheep and Cattle
POM-VPSZoetis Belgium S.A.
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