Characteristics:
| Type |
Vaccine |
| Purpose |
Rabies vaccine |
| Packaging |
1ml
|
| Country of origin |
France |
Description:
Inactivated vaccine against animal rabies
Instruction
Annex 2 of the registration certificate: N° VA-00804-02-16
Composition
One dose of the vaccine contains:
Active substance:
Rabies virus glycoproteins, strain G52 ... > 1 MO; adjuvant;
Aluminum hydroxide ...... 1.7 mg; Additives are added to make 1 dose.
Pharmaceutical form: suspension
Immunobiological properties
The vaccine stimulates active immunity against rabies in animals.
Period of decline of immunity: 2 to 4 weeks. Duration of immunity: for 3 years after the first revaccination of cats and dogs and for one year in the case of deer, horses, cattle and sheep.
Animal species
Dogs, cats, dogs, horses, cattle, sheep.
destination
The vaccine is intended to immunize dogs, cats, dogs, horses, cattle and sheep against rabies.
Contraindication
In the case of horses, vaccination should not be done by the subcutaneous method.
Warnings for use
Vaccination is intended only for clinically healthy animals. Deworming is mandatory at least 10 days before vaccination.
Interaction with other means
Do not mix with other veterinary immunobiological agents. The rabiesin vaccine can be given on the same day but separately from the Boehringer Ingelheim leukemia vaccines and the various combinations of Boehringer Ingelheim components used against viral rhinotracheitis, calicivirus, panleukopenia, and feline chlamydia.
Special instructions during pregnancy and lactation
During the vaccination period, no complications were detected in pregnant animals.
Method of administration and dosage
The vaccine is injected subcutaneously in the case of cats, dogs, ferrets, cattle and sheep, and intramuscularly in the case of horses, in a dose of 1 ml (1 dose), according to the following vaccination scheme:
|
type of animal
|
Primary vaccination
|
Revaccination |
|
Dogs, cats
|
A single dose (1 ml) of the vaccine is used after birth, from 12 weeks of age*
|
One year after the first vaccination
then at intervals of up to 3 years**
|
|
Chowders
|
One dose of the vaccine (1 ml) is used after birth, from the age of 12 weeks
|
annually
|
| Horses, cattle, sheep |
A single dose (1 ml) of the vaccine is used after birth, from the age of 4 months***
|
annually
|
*If the animal was vaccinated before 12 weeks of age, a revaccination at 12 weeks of age or later should be added to the primary vaccination schedule.
**In any case, the revaccination period must comply with the current legislation of the country.
If the animal was vaccinated before 4 months of age, a revaccination at 4 months of age or later should be added to the primary vaccination schedule.
Side effects
In rare cases, vaccination may cause a hypersensitivity reaction. In this case, symptomatic treatment is necessary. A temporary lump may appear at the injection site.
Withdrawal period
is not.
Special warnings for service personnel
General rules of asepsis and antiseptics should be observed during vaccination. In case of accidental injection, it is necessary to seek immediate medical help.
Special precautions for handling unused vaccines, methods of its decontamination
Dispose of vials and vaccine waste in accordance with local regulations.
The shelf life is 36 months.
Shelf life after first opening: Use immediately.
Storage and transportation conditions
Store and transport at 2°C to 8°C, protected from light.
packing
Description of the primary packaging of the vaccine:
Glass vial of type I, 1 or 10 doses of vaccine.
The package includes 1 vial with 10 doses of vaccine or 100 vials with 1 dose of vaccine.
Name and location of trade authorization holder
Boehringer Ingelheim Bears GmbH
55216 Ingelheim am Rhein, Germany
Manufacturer's name and location
Boehringer Ingelheim Animal Health France
Porte des Alpes Laboratory, Route de la 69800, Saint Priest, France.
Dispensing rule
based on the recipe
If the medication does not meet the requirements of the instructions or there are complications, the use of this batch is immediately stopped and the State Research and Control Institute of Biotechnology and Microorganism Strains and the supplier (manufacturer) are notified. Together with the State Research and Control Institute of Biotechnology and Microorganism Strains, three unopened vials of the medicine of this series are sent to the State Veterinary Agency, "On the Procedure for Submitting a Complaint on Biological Medicines for Veterinary Medicine" Law No. 03.06.98 No. According to 2, address: Kyiv, Donetsk street, number 30.
