Procyon Dog DA2PPi/L

Dogs

Procyon Dog DA2PPi/L Data Sheet

Presentation
Lyophilisate and solvent for suspension for injection containing per dose of reconstituted vaccine:
4.5 – 6.0 log10 TCID50 live attenuated Canine distemper virus (Distemperoid strain); 3.9 - 6.0 log10 TCID50 live attenuated Canine adenovirus-2 (Ditchfield strain); 5.2 – 6.0 log10 TCID50 live attenuated Canine parvovirus (SAH 2b strain) and 4.8 – 7.0 log10 TCID50 live attenuated Canine parainfluenza virus (Philips Roxane strain) and > 40 Hamster PD80 inactivated Leptospira interrogans serovar icterohaemorrhagiae (strain 115) and > 40 Hamster PD80 inactivated Leptospira interrogans serovar canicola (strain 117).
Also contains 1.63 – 2.21 mg/ds Aluminium hydroxide as an adjuvant.
 
Uses
For the active immunisation of dogs from 6 weeks of age:
  • to prevent mortality and reduce clinical signs of disease caused by canine distemper virus, canine parvovirus and infectious canine hepatitis.
  • to prevent mortality and reduce clinical signs of disease caused by Leptospira interrogans serovars canicola and icterohaemorrhagiae.
  • to reduce clinical signs and viral shedding of canine adenovirus type 2.
  • to reduce viral shedding of canine parainfluenza virus and canine parvovirus.
Immunity has been demonstrated from:
  • 3 weeks after the first dose for parvovirus.
  • 3 weeks after the primary vaccination course for distemper.
  • 4 weeks after the primary vaccination course for canine adenovirus and Leptospira interrogans serovars canicola and icterohaemorrhagiae.3 weeks after the primary vaccination course (serological response only) for parainfluenza.

Duration of immunity is 4 years for distemper, adenovirus (CAV1 and CAV2) and parvovirus and 12 months by challenge for parainfluenza and Leptospira interrogans serovars canicola and icterohaemorrhagiae.

Dosage and administration 
Each dose is prepared by reconstituting a vial of freeze dried (DA2PPi) fraction with a vial of liquid (L) vaccine. The reconstituted vaccine should be gently shaken and given immediately by subcutaneous or intramuscular injection.
 
Primary vaccination
Two doses of 1 ml given with an interval of 3-4 weeks.
Dogs and puppies 6 weeks of age and over:
Administer one dose by i.m. or s.c. injection, then a second dose 3 to 4 weeks later, but not before 10 weeks of age.
 
Booster vaccination
Dose: 1 ml.
In order to maintain immunity against CPi, L. icterohaemorrhagiae and L. canicola, annual revaccination is required against these components. To maintain immunity against CPV, CDV and CAV revaccination at intervals of up to 4 years is required.
 
Contra-indications, warnings, etc
Do not use in dogs that have been treated with immunosuppressive drugs or hyperimmune serum within the last month.
 
No information is available on the use of the vaccine in pregnant bitches. Do not use in pregnant or lactating bitches. Pregnant bitches should not come into contact with recently vaccinated animals.
Following primary vaccination, dogs should remain isolated from possible sources of infection for at least 7 days to reduce risk of interference with the immune response.
 
The presence of maternally derived antibodies (MDA) in young puppies may interfere with the development of a protective immune response following vaccination. Nevertheless, the vaccine has been demonstrated to be efficacious in puppies with moderate levels of MDA to canine distemper virus (CDV), canine parvovirus (CPV), and canine adenovirus (CAV). Intramuscular vaccination gives a slightly higher serological response than subcutaneous vaccination. Thus, if particularly high and persistent levels of MDA against CPV or CDV are suspected or measured (e.g. for CDV >30 units SN at first vaccination) then intramuscular vaccination is recommended and the first vaccination should be delayed to 8 weeks of age.
 
Following vaccination, the vaccine viruses CAV-2 and CPV will be excreted and can spread to unvaccinated animals in contact but will not cause disease. Canine parainfluenza (CPi) may also be excreted but will not spread.
Cats (a non-target species) are known to be susceptible to CPV, and therefore in-contact animals may develop antibodies but not disease.
Avoid intradermal vaccination.
 
A mild (<1 cm3), transient, local swelling may infrequently be seen at the injection site after the first intramuscular vaccination, which resolves completely without complication within a maximum of 3 weeks. Swelling commonly occurs at the injection site after the first or second subcutaneous vaccination; this swelling was up to 7.7 cm3 (4 cm diameter) after the first vaccination and resolved within 2 weeks without complication. In rare cases the swelling may be severe. In rare cases diarrhoea may be observed after vaccination and after intramuscular vaccination a single case (1%) of transient (1-2 day duration) lameness was observed.
Occasional hypersensitivity reactions may rarely occur. In such cases appropriate treatment, such as adrenaline or antihistamine, should be administered without delay. Dogs which receive an overdose of vaccine will exhibit similar adverse effects as described above. Local swelling at the injection site (particularly when subcutaneous injection is used) may be larger (up to 10.7 cm3) and take longer to resolve (up to 33 days).
 
Interactions
No information is available on the safety and efficacy from the concurrent use of this vaccine with any other. It is therefore recommended that no other vaccines should be administered within 14 days before or after vaccination with the product.
Do not mix with any other vaccine/immunological product.
 
Operator warnings
In the case of accidental self-injection or ingestion seek medical advice immediately and show the package leaflet or label to the physician.
 
Withdrawal period
Not applicable.
For animal treatment only. Keep out of reach and sight of children.
 
Pharmaceutical precautions
Store and transport refrigerated between +2 °C and +8 °C. Protect from light. Do not freeze.
Use the vaccine immediately after reconstitution.
 
Disposal advice
Any unused product or waste material should be disposed of by boiling, incineration or immersion in an appropriate disinfectant in accordance with national requirements.
 
Legal category
POM-V      - To be supplied only on veterinary prescription
 
Packaging Quantities
Cardboard pack containing 10 vials of DA2PPi and 10 of L.
Cardboard pack containing 25 vials of DA2PPi and 25 of L.

Further information

Nil.
 
Marketing authorisation number
Vm 00201/4199.