ReproCyc PRRS EU lyophilisate and solvent for suspension for injection for pigs

País: Irlanda

Idioma: inglés

Fuente: HPRA (Health Products Regulatory Authority)

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Ficha técnica Ficha técnica (SPC)
12-06-2017

Ingredientes activos:

Live attenuated prrs 94881 virus

Disponible desde:

Boehringer Ingelheim Ltd

Código ATC:

QI09AD03

Designación común internacional (DCI):

Live attenuated prrs 94881 virus

Dosis:

.

formulario farmacéutico:

Lyophilisate + solvent for suspension

tipo de receta:

POM: Prescription Only Medicine as defined in relevant national legislation

Grupo terapéutico:

Pigs

Área terapéutica:

porcine reproductive and respiratory syndrome (PRRS) virus

indicaciones terapéuticas:

Immunological - Live Vaccine

Estado de Autorización:

Authorised

Fecha de autorización:

2015-04-02

Ficha técnica

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
ReproCyc PRRS EU lyophilisate and solvent for suspension for injection
for pigs.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose (2 ml) contains:
Lyophilisate:
ACTIVE SUBSTANCE
Live attenuated Porcine Respiratory and Reproductive Syndrome Virus
(PRRSV), strain 94881 (genotype 1)
At least: 10
TCID
10
TCID
*Tissue Culture Infectious Dose 50
Solvent:
ADJUVANT
Carbomer: 2.0 mg
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Lyophilisate and solvent for suspension for injection.
Lyophilisate: off-white to milky grey
Solvent: clear, colourless solution
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Pigs (breeding females)
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For active immunisation of breeding females from farms affected with
European (genotype 1) Porcine Reproductive
and Respiratory Syndrome Virus (PRRSV) to reduce the duration of
viraemia, the proportion of viraemic gilts/sows
and viral loads in blood after exposure to PRRSV as shown under
experimental conditions.
Onset of immunity:
4 weeks
Duration of immunity:
17 weeks
Vaccination of breeding females according to the recommended schedule
described in section 4.9 reduces the negative
reproductive disorders associated with PRRSV.
Under experimental challenge conditions a reduction in transplacental
virus transmission after challenge was
additionally demonstrated. In piglets from vaccinated sows, a
reduction in the negative impact of PRRS virus infection
(mortality, clinical signs and weight gain) was also demonstrated
during the first 20 days of life.
3.9
50
-
7.0
50
*
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