Nobivac Solvent

Country: Ireland

Language: English

Source: HPRA (Health Products Regulatory Authority)

Available from:

Intervet Ireland Limited

ATC code:

QV07AB

Dosage:

.

Pharmaceutical form:

Solvent for parenteral use

Prescription type:

POM: Prescription Only Medicine as defined in relevant national legislation

Therapeutic group:

Cats, Dogs

Therapeutic area:

Solvents and diluting agents, incl. irrigating solutions

Therapeutic indications:

Immunological - Diluent

Authorization status:

Authorised

Authorization date:

2003-10-03

Summary of Product characteristics

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobivac Solvent
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
ACTIVE SUBSTANCES:
None
EXCIPIENTS:
For the full list of excipients, see section 6.1
3 PHARMACEUTICAL FORM
Solvent for parenteral use.
Clear, colourless liquid.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cats and dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Solvent for reconstitution of Nobivac DHP, Nobivac DHPPi, Nobivac
Parvo-C, Nobivac Ducat and Nobivac Tricat
Trio vaccines.
4.3 CONTRAINDICATIONS
Any contra-indications specified for the vaccine for which the solvent
is used for reconstitution will apply.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
There are no special warnings, however any warnings specified for the
vaccine for which Nobivac Solvent is used as
the solvent will apply.
4.5 SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
No special precautions are required for handling the solvent however
any recommendations specified for the vaccine
for which Nobivac Solvent is used as a solvent will apply.
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.
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