Rabisin

Land: Irland

Språk: engelsk

Kilde: HPRA (Health Products Regulatory Authority)

Aktiv ingrediens:

Rabies virus glycoprotein

Tilgjengelig fra:

Merial Animal Health Limited

ATC-kode:

QI07AA02

INN (International Name):

Rabies virus glycoprotein

Dosering :

.

Legemiddelform:

Suspension for injection

Resept typen:

POM: Prescription Only Medicine as defined in relevant national legislation

Terapeutisk gruppe:

Cats, Cattle, Dogs, Horses, Other Mammals, Sheep

Terapeutisk område:

rabies virus

Indikasjoner:

Immunological - Inactivated Vaccine

Autorisasjon status:

Authorised

Autorisasjon dato:

2004-08-10

Preparatomtale

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Rabisin
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Suspension for injection.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle, dogs, horses, cats, mustelids and sheep
.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For active immunisation of cattle, dogs, horses, cats, mustelids and
sheep, to reduce mortality and clinical signs due to
rabies infection.
Immunity has been demonstrated 1 month after primary vaccination, and
has been shown to persist up to the first
booster dose (1 year after primary vaccination).
In cats and dogs immunity has been shown to persist for up to 3 years
following booster vaccination.
4.3 CONTRAINDICATIONS
Do not inject the vaccine subcutaneously in horses. Do not inject the
vaccine intramuscularly in cats and dogs.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
Do not vaccinate unhealthy animals
.
Each 1 ml dose of vaccine contains:
ACTIVE SUBSTANCE(S):
Rabies virus glycoproteins
1 IU
ADJUVANT(S):
Aluminium (as hydroxide)
1.7
mg
EXCIPIENT(S):
Excipient
q.s.
1
ml
For a full list of excipients, see section 6.1.
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4.5 SPECIAL PRECAUTIONS FOR USE
(I) SPECIAL PRECAUTIONS FOR USE IN ANIMALS:
Where a dog or cat was vaccinated before 12 weeks of age, the primary
vaccination sc