Versican Plus DHPPi Lyophilisate and Solvent for Suspension for Injection for Dogs
Active ingredients: Canine adenovirus, Canine distemper virus, Canine parainfluenza virus, Canine parvovirus
Form
Injection
Species
Manufacturer
Zoetis UK Limited
VMD MA No.
42058/5082
What it's used for
Active immunisation of dogs from 6 weeks of age: to prevent mortality and clinical signs caused by canine distemper virus, to prevent mortality and clinica...
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Prescription required
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Versican Plus DHPPi Lyophilisate and Solvent for Suspension for Injection for Dogs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
to prevent mortality and clinical signs caused by canine distemper virus,
to prevent mortality and clinical signs caused by canine adenovirus type 1,
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to prevent clinical signs and reduce viral excretion caused by canine adenovirus type
2,
to prevent clinical signs, leucopoenia and viral excretion caused by canine
parvovirus and
to prevent clinical signs (nasal and ocular discharge) and reduce viral excretion
caused by canine parainfluenza virus.
Onset of immunity:
3 weeks after the first vaccination for CDV, CAV, CPV, and
3 weeks after completion of the primary course for CPiV.
Duration of immunity:
At least three years following the primary vaccination course for canine distemper
virus, canine adenovirus type 1, canine adenovirus type 2 and canine parvovirus.
The duration of immunity against CAV-2 was not established by challenge. It was
shown that 3 years after the vaccination CAV-2 antibodies are still present.
Protective immune response against CAV-2 associated respiratory disease is
considered to last at least 3 years. At least one year following the primary
vaccination course for canine parainfluenza virus.
Common
(1 to 10 animals / 100 animals
treated):
injection site swelling
Rare
(1 to 10 animals / 10,000 animals
treated):
hypersensitivity reaction
(anaphylaxis,
angioedema, circulatory shock, collapse,
diarrhoea, dyspnoea, vomiting)
anorexia, decreased activity
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
hyperthermia, lethargy, malaise
A transient swelling (up to 5 cm) which can be painful, warm or reddened. Any such
swelling will either have spontaneously resolved or be greatly diminished by 14 days
after vaccination.
If a hypersensitivity reaction occurs, appropriate treatment should be administered
without delay. Such reactions may evolve to a more severe condition which may be
life-threatening.
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 section 16 of the
package leaflet for contact details.
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Immunocompetence of the animal may be compromised by a variety of factors
including poor health, nutritional status, genetic factors, concurrent medicinal therapy
and stress.
Immunological responses to the CDV, CAV and CPV components of the vaccine
may be delayed due to maternally derived antibody interference. However, the
vaccine has been proven to be protective against virulent challenge in the presence
of maternally derived antibodies to CDV, CAV and CPV at levels equal or higher to
those likely to be encountered under field conditions. In situations where very high
maternally derived antibody levels are expected, the vaccination protocol should be
planned accordingly.
Vaccinate healthy animals only.
Special precautions for use in animals
The live attenuated virus vaccine strains CAV-2, CPiV and CPV-2b may be shed by
vaccinated dogs following vaccination, shedding of CPV has been shown for up to
10 days. However, due to the low pathogenicity of these strains, it is not necessary
to keep vaccinated dogs separated from non-vaccinated dogs and domestic cats.
The vaccine virus strain CPV-2b has not been tested in other carnivores (except
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dogs and domestic cats) that are known to be susceptible to canine parvoviruses
and therefore vaccinated dogs should be separated from them after vaccination.
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.
Other precautions
Not applicable.
any other veterinary medicinal product other than Versiguard Rabies and Versican
Plus L4. 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.
Leptospira:
If protection against is required, dogs can be vaccinated with two doses
of Versican Plus DHPPi mixed with Versican Plus L4 3–4 weeks apart from 6 weeks
of age:
The contents of a single vial of Versican Plus DHPPi should be reconstituted with the
contents of a single vial of Versican Plus L4 (instead of the solvent). Once mixed, the
contents of the vial should appear a pinkish or yellowish colour with light
opalescence. The mixed vaccines should be injected immediately via the
subcutaneous route.
Rabies:
If protection against rabies is required:
First dose: Versican Plus DHPPi from 8–9 weeks of age.
Second dose: Versican Plus DHPPi mixed with Versiguard Rabies 3–4 weeks later,
but not before 12 weeks of age.
The contents of a single vial of Versican Plus DHPPi should be reconstituted with the
contents of a single vial of Versiguard Rabies (instead of the solvent). Once mixed,
the contents of the vial should appear a pink/red or yellowish colour with light
opalescence. The mixed vaccines should be injected immediately via the
subcutaneous route.
The efficacy of the rabies fraction is proven after a single dose from 12 weeks of age
in laboratory studies. However, in field studies 10% of seronegative dogs did not
show seroconversion (>0.1 IU/ml) 3–4 weeks after single primary vaccination against
rabies. Some animals may also not show titres > 0.5 IU/ml after the primary
vaccination. Antibody titres drop over the course of the 3-year duration of immunity,
although dogs are protected when challenged. In case of travelling to risk areas or
outside the EU, veterinary surgeons may wish to give additional rabies vaccinations
after 12 weeks of age to ensure that the vaccinated dogs have an antibody titre of
≥ 0.5 IU/ml, which is generally regarded as sufficiently protective and that they meet
the travel test requirements (antibody titres ≥ 0.5 IU/ml).
Although the efficacy of the rabies fraction has been demonstrated following
administration at 12 weeks, at the discretion of the veterinary surgeon, in case of
need, dogs younger than 8 weeks can be vaccinated with Versican Plus DHPPi
mixed with Versiguard Rabies as the safety of this association has been
demonstrated in 6-week old dogs.
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AN: 03023/2023
Do not freeze.
Protect from light.
Canine adenovirus Type 2, strain CAV-2 Bio 13 10
3.6
TCID50*
5.3
TCID50*
Canine parvovirus Type 2b, strain CPV-2b Bio 12/B 10
4.3
TCID50* 10
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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Related Conditions
Other Products Containing Canine adenovirus
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Canigen DHP Lyophilisate and Solvent for Suspension for Injection for Dogs
POM-VIntervet International B.V.
Canigen DHPPi Lyophilisate for Suspension for Injection for Dogs
POM-VIntervet International B.V.
Canixin DHPPi Lyophilisate and Solvent for Suspension for Injection for Dogs
POM-VVirbac
Canixin DHPPi Lyophilisate and Solvent for Suspension for Injection for Dogs
POM-VVirbac
Canixin DHPPi/L
POM-VVIRBAC
CANIXIN DHPPi/L Lyophilisate and Suspension for Suspension for Injection for Dogs
POM-VVirbac
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