Nobivac Rabies, 1 ml / 1 dose. Against rabies

Nobivac Rabies, 1 ml / 1 dose. Against rabies

$10.00

Nobivac Rabies 1 ml / 1 dose, suspension for the active immunisation of healthy dogs, cats, cattle, sheep, goats, ferrets, foxes and horses, and in principle all healthy mammals against rabies.

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Description

Buy online Nobivac Rabies 1 ml / 1 dose, suspension for the active immunisation of healthy dogs, cats, cattle, sheep, goats, ferrets, foxes and horses, and in principle all healthy mammals against rabies.
INGREDIENTS:
Active substance: Rabies strain Pasteur RIV: at least 2 I.U. per dose;
Preservative: Thiomersal 0.01%.

DESCRIPTION:
Nobivac Rabies — this vaccine contains an inactivated culture of rabies virus, cloned out of strain Pasteur RIV with a potency of ≥ 2 I.U. The virus is grown on the BHK-21 clone CT cell line and inactivated with beta-propiolactone. It is presented as an aluminium phosphate adsorbed vaccine.
PHARMACEUTICAL PARTICULARS:
Incompatibilities: Do not mix with any other veterinary medicinal product.

INDICATIONS::
For the active immunisation of healthy dogs, cats, cattle, sheep, goats, ferrets, foxes and horses, and in principle all healthy mammals against rabies.

CONTRAINDICATIONS, WARNINGS, etc:
Do not use Nobivac Rabies in unhealthy animals.
The vaccine may not be effective in animals incubating the disease at the time of vaccination. A good immune response is reliant on the reaction of an immunogenic agent and a fully competent immune system. Immunogenicity of the vaccine antigen will be reduced by poor storage or inappropriate administration. Immunocompetence of the animal may be compromised by a variety of factors including poor health, nutritional status, genetic factors, concurrent drug therapy and stress.
Some animals may be immunologically incompetent and fail to respond to vaccination. Animals that have received the corresponding anti-serum or immunosuppressive drugs should not be vaccinated until an interval of at least 4 weeks has elapsed.
Transient local reactions such as non-painful diffuse to firm swellings of approximately 1 cm in diameter may be observed for up to 3 weeks after subcutaneous vaccination. In the rare event of a hypersensitivity reaction following vaccination, administer an antihistamine, corticosteroid or adrenaline, without delay and by the most immediate route.
After administration of an overdose no effects other than those described above occurred. The presence of maternal antibodies can interfere with the response to vaccination.
Can be used during pregnancy in dogs. There are no laboratory data on use during pregnancy in other species, but on the basis of field experience, such use is expected to be safe.
Safety and efficacy data are available which demonstrate that this vaccine can be used to reconstitute the freeze dried Intervet vaccines of the Nobivac range containing one or more of the following: live canine distemper, canine adenovirus, canine parvovirus and canine parainfluenza and inactivated canine leptospirosis antigens or live feline viral rhinotracheitis virus, feline calicivirus and feline panleucopenia virus.
No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product except the products mentioned above. 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.
This product should not be given for at least one month following the administration of hyperimmune serum or immunosuppressant drugs.
Do not mix with any other veterinary medicinal products apart from those listed above..

INTERACTION with OTHER MEDICINAL PRODUCTS and other forms of interaction:
Nobivac Rabies can be used to reconstitute the freeze-dried canine vaccines of the Nobivac series.
Nobivac Rabies can be administered with the Nobivac leptospirosis vaccines at the same time but at a different administration site.
No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product except the products mentioned above. 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.

ADVERS REACTIONS:
None.

INTERACTION WITH OTHER MEDICAMENTS:
None known.

OVERDOSE:
After subcutaneous administration occasionally a transient palpable nodule may occur at the site of injection.

WITHDRAWAL PERIOD:
Not applicable.

SHELF LIFE:
At least 4 years at 2°C – 8°C.
Broached vials of the 10-dose presentation should be used within one working day.

SPECIAL PRECAUTIONS for STORAGE:
For animal treatment only. Keep out of reach and sight of children.
Store in a refrigerator (2°C to 8°C). Do not freeze.
Protect from light.

PACKAGING:
Cartons with 1, 10 or 50 glass type I vials with 1 ml, and carton with 1 vial of type I with 10 ml, with a rubber stopper and aluminium cap. Not all presentations may be marketed.

Additional information

Weight 50 g
Forms of release

Suspension

Volume / Weight

10 ml

Packing

Glass bottle

Manufacturer

INTERVET INTERNATIONAL B.V. BOXMEER

Country/Region of Manufacture

Netherlands

DOSAGE AND ADMINISTRATION:
A single dose inoculation of 1 ml is sufficient irrespective of size, species or breed of animal. Sterile equipment should be used for administration. Avoid contamination of vaccine with traces of chemical sterilising agents. Do not use chemicals such as disinfectant or spirit to disinfect the skin prior to inoculation.
Primary vaccination age* 3 months or older.
Route of administration intramuscularly or subcutaneously.
* Primary vaccination may be administered at an earlier age (minimum in dogs and cats of 4 weeks of age), but then a repeat vaccination must be given at the age of 3 months.
Can be used during pregnancy in dogs.

RECOMMENDED VACCINATION PROGRAMME:

Dogs/Cats Cattle/Horses Ferrets
Primary vaccination
at an age of more than
3 months* 6 months* 3 months*
Revaccination every 3 years** 2 years** 1 year**
Route of
administration
i.m. or s.c. i.m. s.c.

*Primary vaccination can be administered at an earlier age, but then a repeat vaccination must be given at the age of 3 or 6 months depending on the species.
**Recommended revaccination interval is based upon results from challenge experiments. Local regulations in force may require earlier revaccination.
Results from serological investigations indicate that vaccination of sheep, goats, and foxes provides protection for at least one year.

VACCINATION REACTIONS:
After subcutaneous administration occasionally a transient palpable nodule may occur at the site of injection.

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