Veraflox

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
08-04-2020
Scheda tecnica Scheda tecnica (SPC)
08-04-2020

Principio attivo:

pradofloxacin

Commercializzato da:

Bayer Animal Health GmbH 

Codice ATC:

QJ01MA97

INN (Nome Internazionale):

pradofloxacin

Gruppo terapeutico:

Dogs; Cats

Area terapeutica:

Antibacterials for systemic use, Fluoroquinolones

Indicazioni terapeutiche:

DogsTreatment of:wound infections caused by susceptible strains of the Staphylococcus intermedius group (including S. pseudintermedius);superficial and deep pyoderma caused by susceptible strains of the Staphylococcus intermedius group (including S. pseudintermedius);acute urinary-tract infections caused by susceptible strains of Escherichia coli and the Staphylococcus intermedius group (including S. pseudintermedius);as adjunctive treatment to mechanical or surgical periodontal therapy in the treatment of severe infections of the gingiva and periodontal tissues caused by susceptible strains of anaerobic organisms, for example Porphyromonas spp. and Prevotella spp.CatsTreatment of acute infections of the upper respiratory tract caused by susceptible strains of Pasteurella multocida, Escherichia coli and the Staphylococcus intermedius group (including S. pseudintermedius).

Dettagli prodotto:

Revision: 8

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2011-04-12

Foglio illustrativo

                                36
B. PACKAGE LEAFLET
37
PACKAGE LEAFLET:
VERAFLOX 15 MG TABLETS FOR DOGS AND CATS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder :
Bayer Animal Health GmbH
D-51368 Leverkusen
Germany
Manufacturer responsible for batch release:
KVP Pharma +Veterinär Produkte GmbH
Projensdorfer Str. 324
D-24106 Kiel
Germany
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Veraflox 15 mg tablets for dogs and cats
pradofloxacin
3.
STATEMENT OF THE ACTIVE SUBSTANCE AND OTHER INGREDIENTS
Each tablet contains:
ACTIVE SUBSTANCE:
Pradofloxacin
15 mg
Brownish single-scored tablets with “P15” on one side
The tablet can be divided into equal doses.
4.
INDICATIONS
Dogs:
Treatment of:
•
wound infections caused by susceptible strains of the
_Staphylococcus intermedius_
group
(including
_S. pseudintermedius_
),
•
superficial and deep pyoderma caused by susceptible strains of the
_Staphylococcus intermedius_
group (including
_S. pseudintermedius_
),
_ _
•
acute urinary tract infections caused by susceptible strains of
_Escherichia coli_
and the
_Staphylococcus intermedius_
group (including
_S. pseudintermedius_
) and
•
as adjunctive treatment to mechanical or surgical periodontal therapy
in the treatment of severe
infections of the gingiva and periodontal tissues caused by
susceptible strains of anaerobic
organisms, for example
_Porphyromonas_
spp. and
_Prevotella_
spp. (see section “Special
Warnings”).
Cats:
38
Treatment of:
•
acute infections of the upper respiratory tract caused by susceptible
strains of
_Pasteurella _
_multocida_
,
_Escherichia coli_
and the
_Staphylococcus intermedius _
group (including
_S. pseudintermedius_
).
5.
CONTRAINDICATIONS
-
Do not use in cases of hypersensitivity to the active substances or to
any of the excipients.
Dogs:
Do not use in dogs during the period of growth as developing articular
cartilage may be affected. The
period of growth depends on the breed. For the ma
                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                1
_ _
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Veraflox 15 mg tablets for dogs and cats
Veraflox 60 mg tablets for dogs
Veraflox 120 mg tablets for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains:
ACTIVE SUBSTANCE:
Pradofloxacin
15 mg
Pradofloxacin
60 mg
Pradofloxacin
120 mg
EXCIPIENTS:
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablets.
Brownish single-scored tablets with “P15” on one side
Brownish single-scored tablets with “P60” on one side
Brownish single-scored tablets with “P120” on one side
The tablet can be divided into equal doses.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs, cats
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Dogs:
Treatment of:
•
wound infections caused by susceptible strains of the
_Staphylococcus intermedius_
group
(including
_S. pseudintermedius_
),
•
superficial and deep pyoderma caused by susceptible strains of the
_Staphylococcus intermedius_
group (including
_S. pseudintermedius_
),
_ _
•
acute urinary tract infections caused by susceptible strains of
_Escherichia coli_
and the
_Staphylococcus intermedius_
group (including
_S. pseudintermedius_
) and
•
as adjunctive treatment to mechanical or surgical periodontal therapy
in the treatment of severe
infections of the gingiva and periodontal tissues caused by
susceptible strains of anaerobic
organisms, for example
_Porphyromonas_
spp. and
_Prevotella_
spp. (see section 4.5).
Cats:
3
Treatment of acute infections of the upper respiratory tract caused by
susceptible strains of
_Pasteurella_
_multocida_
,
_Escherichia coli_
and the
_Staphylococcus intermedius _
group (including
_S. pseudintermedius_
)
_._
4.3
CONTRAINDICATIONS
Do not use in cases of hypersensitivity to the active substance or to
any of the excipients.
Dogs:
Do not use in dogs during the period of growth as developing articular
cartilage may be affected. The
period of growth depends on the breed. For the majority of breeds,
pradofloxacin-c
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 08-04-2020
Scheda tecnica Scheda tecnica bulgaro 08-04-2020
Foglio illustrativo Foglio illustrativo spagnolo 08-04-2020
Scheda tecnica Scheda tecnica spagnolo 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 18-07-2011
Foglio illustrativo Foglio illustrativo ceco 08-04-2020
Scheda tecnica Scheda tecnica ceco 08-04-2020
Foglio illustrativo Foglio illustrativo danese 08-04-2020
Scheda tecnica Scheda tecnica danese 08-04-2020
Foglio illustrativo Foglio illustrativo tedesco 08-04-2020
Scheda tecnica Scheda tecnica tedesco 08-04-2020
Foglio illustrativo Foglio illustrativo estone 08-04-2020
Scheda tecnica Scheda tecnica estone 08-04-2020
Foglio illustrativo Foglio illustrativo greco 08-04-2020
Scheda tecnica Scheda tecnica greco 08-04-2020
Foglio illustrativo Foglio illustrativo francese 08-04-2020
Scheda tecnica Scheda tecnica francese 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 18-07-2011
Foglio illustrativo Foglio illustrativo italiano 08-04-2020
Scheda tecnica Scheda tecnica italiano 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 18-07-2011
Foglio illustrativo Foglio illustrativo lettone 08-04-2020
Scheda tecnica Scheda tecnica lettone 08-04-2020
Foglio illustrativo Foglio illustrativo lituano 08-04-2020
Scheda tecnica Scheda tecnica lituano 08-04-2020
Foglio illustrativo Foglio illustrativo ungherese 08-04-2020
Scheda tecnica Scheda tecnica ungherese 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 18-07-2011
Foglio illustrativo Foglio illustrativo maltese 08-04-2020
Scheda tecnica Scheda tecnica maltese 08-04-2020
Foglio illustrativo Foglio illustrativo olandese 08-04-2020
Scheda tecnica Scheda tecnica olandese 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 18-07-2011
Foglio illustrativo Foglio illustrativo polacco 08-04-2020
Scheda tecnica Scheda tecnica polacco 08-04-2020
Foglio illustrativo Foglio illustrativo portoghese 08-04-2020
Scheda tecnica Scheda tecnica portoghese 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 18-07-2011
Foglio illustrativo Foglio illustrativo rumeno 08-04-2020
Scheda tecnica Scheda tecnica rumeno 08-04-2020
Foglio illustrativo Foglio illustrativo slovacco 08-04-2020
Scheda tecnica Scheda tecnica slovacco 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 18-07-2011
Foglio illustrativo Foglio illustrativo sloveno 08-04-2020
Scheda tecnica Scheda tecnica sloveno 08-04-2020
Foglio illustrativo Foglio illustrativo finlandese 08-04-2020
Scheda tecnica Scheda tecnica finlandese 08-04-2020
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 18-07-2011
Foglio illustrativo Foglio illustrativo svedese 08-04-2020
Scheda tecnica Scheda tecnica svedese 08-04-2020
Foglio illustrativo Foglio illustrativo norvegese 08-04-2020
Scheda tecnica Scheda tecnica norvegese 08-04-2020
Foglio illustrativo Foglio illustrativo islandese 08-04-2020
Scheda tecnica Scheda tecnica islandese 08-04-2020
Foglio illustrativo Foglio illustrativo croato 08-04-2020
Scheda tecnica Scheda tecnica croato 08-04-2020

Cerca alert relativi a questo prodotto

Visualizza cronologia documenti