Spironolactone Ceva

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

spironolakton

Available from:

Ceva Santé Animale

ATC code:

QC03DA01

INN (International Name):

spironolactone

Therapeutic group:

Psi

Therapeutic area:

Diuretiki

Therapeutic indications:

Za uporabo v kombinaciji s standardno terapijo (vključno z diuretiki podporo, kadar je to potrebno) za zdravljenje kongestivnega srčnega popuščanja zaradi valvular regurgitacija v psi.

Product summary:

Revision: 7

Authorization status:

Umaknjeno

Authorization date:

2007-06-20

Patient Information leaflet

                                22
B. NAVODILO ZA UPORABO
23
NAVODILO ZA UPORABO:
Spironolactone Ceva 10 mg tablete za pse
Spironolactone Ceva 40 mg tablete za pse
Spironolactone Ceva 80 mg tablete za pse
1.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM TER
IMETNIKA DOVOLJENJA ZA IZDELAVO ZDRAVILA, ODGOVORNEGA ZA
SPROSTITEV SERIJE V EGP, ČE STA RAZLIČNA
Imetnik dovoljenja za promet z zdravilom:
Ceva Santé Animale
10 avenue de la Ballastière
33500 Libourne
Francija
Tel: + 33 (0) 5 57 55 40 40
Fax: + 33 (0) 5 57 55 41 98
Izdelovalec, odgovoren za sprostitev serije:
Ceva Santéanimale
Z.I. Très le Bois
22600 Loudéac
Francija
Catalent Germany
Schorndorf GmbH
Steinbeistrasse 2
D-73614 Schorndorf
Nemčija
2.
IME ZDRAVILA ZA UPORABO V VETERINARSKI MEDICINI
Spironolactone Ceva 10 mg tablete za pse
Spironolactone Ceva 40 mg tablete za pse
Spironolactone Ceva 80 mg tablete za pse
Spironolakton
3.
NAVEDBA ZDRAVILNE UČINKOVINE IN DRUGIH SESTAVIN
Spironolactone Ceva 10 mg vsebuje 10 mg spironolaktona
Spironolactone Ceva 40 mg vsebuje 40 mg spironolaktona
Spironolactone Ceva 80 mg vsebuje 80 mg spironolaktona
4.
INDIKACIJE
Zmanjšanje kardiovaskularnih poškodb pri kongestivni odpovedi srca
povzročeni zaradi valvularne
regurgitacije pri psih v kombinaciji s standardno terapijo, ki
vključuje diuretično podporo, če je
potrebno.
24
5.
KONTRAINDIKACIJE
Ne uporabljajte pri psih, ki so oboleli za hipoadenokorticizmom,
hiperkaliemijo ali hiponatriemijo.
Ne uporabljajte skupaj z nesteroidnimi protivnetnimi zdravili (NSAID)
pri psih z insuficienco
ledvic (okvara ledvic/disfunkcija).
Ne uporabite v obdobju brejostji in laktacije.
Ne uporabite pri vzrejnih živalih.
6.
NEŽELENI UČINKI
Reverzibilna atrofija prostate ( redukcija v velikosti ) je pogosto
opažena pri nekastriranih samcih.
Če opazite kakršne koli resne stranske učinke ali druge učinke, ki
niso omenjeni v teh navodilih za
uporabo, obvestite svojega veterinarja.
7.
CILJNE ŽIVALSKE VRSTE
Psi.
8.
ODMERKI ZA POSAMEZNE ŽIVALSKE VRSTE TER POT(I) IN NAČIN UPORABE
ZDRAVILA
Peroralna up
                                
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Summary of Product characteristics

                                1
DODATEK I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA ZA UPORABO V VETERINARSKI MEDICINI
Spironolactone Ceva 10 mg tablete za pse
Spironolactone Ceva 40 mg tablete za pse
Spironolactone Ceva 80 mg tablete za pse
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
ZDRAVILNA UČINKOVINA:
Spironolactone Ceva 10 mg vsebuje 10 mg spironolaktona
Spironolactone Ceva 40 mg vsebuje 40 mg spironolaktona
Spironolactone Ceva 80 mg vsebuje 80 mg spironolaktona
Za celoten seznam pomožnih snovi, glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
Tableta.
Spironolactone Ceva 10 mg: Rjava, na pol deljiva ovalna tableta
dolžine 10 mm.
Spironolactone Ceva 40 mg: Rjava, na pol deljiva ovalna tableta
dolžine 17 mm.
Spironolactone Ceva 80 mg: Rjava, na štiri dele deljiva ovalna
tableta dolžine 20 mm.
4.
KLINIČNI PODATKI
4.1
CILJNE ŽIVALSKE VRSTE
Psi.
4.2
INDIKACIJE ZA UPORABO PRI CILJNIH ŽIVALSKIH VRSTAH
Zmanjšanje kardiovaskularnih poškodb pri kongestivni odpovedi srca
povzročeni zaradi valvularne
regurgitacije pri psih v kombinaciji s standardno terapijo, ki
vključuje diuretično podporo, če je
potrebno.
4.3
KONTRAINDIKACIJE
Ne uporabite pri psih, ki so oboleli za hipoadenokorticizmom,
hiperkaliemijo ali hiponatriemijo.
Ne uporabite skupaj z nesteroidnimi protivnetnimi zdravili (NSAID) pri
psih z insuficienco ledvic
(ledvično okvaro/disfunkcijo).
Ne uporabite v obdobju brejostji in laktacije.
Ne uporabite pri vzrejnih živalih.
4.4
POSEBNA OPOZORILA ZA VSAKO CILJNO ŽIVALSKO VRSTO
Jih ni.
4.5
POSEBNI PREVIDNOSTNI UKREPI
POSEBNI PREVIDNOSTNI UKREPI ZA UPORABO PRI ŽIVALIH
Pred začetkom kombiniranega zdravljenja s spironolaktonom in
inhibitorji angiotenzin
konvertirajočega encima (ACE) je treba oceniti ledvično funkcijo in
nivo serumskega kalija. Za
razliko od ljudi, se pogostost povečane hiperkalemije ni pokazala pri
kliničnih testiranjih pri psih v
3
omenjeni kombinaciji. Vendar pa pri psih z ledvično oslabelostjo
obstaja tveganje hiperkaliemije in se
zato priporoča redni monitoring ledvične funkcije in nivoja
serumsk
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-11-2017
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-11-2017
Public Assessment Report Public Assessment Report Bulgarian 24-02-2021
Patient Information leaflet Patient Information leaflet Spanish 27-11-2017
Public Assessment Report Public Assessment Report Spanish 24-02-2021
Patient Information leaflet Patient Information leaflet Czech 27-11-2017
Public Assessment Report Public Assessment Report Czech 24-02-2021
Patient Information leaflet Patient Information leaflet Danish 27-11-2017
Public Assessment Report Public Assessment Report Danish 24-02-2021
Patient Information leaflet Patient Information leaflet German 27-11-2017
Public Assessment Report Public Assessment Report German 24-02-2021
Patient Information leaflet Patient Information leaflet Estonian 27-11-2017
Public Assessment Report Public Assessment Report Estonian 24-02-2021
Patient Information leaflet Patient Information leaflet Greek 27-11-2017
Public Assessment Report Public Assessment Report Greek 24-02-2021
Patient Information leaflet Patient Information leaflet English 27-11-2017
Public Assessment Report Public Assessment Report English 24-02-2021
Patient Information leaflet Patient Information leaflet French 27-11-2017
Public Assessment Report Public Assessment Report French 24-02-2021
Patient Information leaflet Patient Information leaflet Italian 27-11-2017
Public Assessment Report Public Assessment Report Italian 18-07-2007
Patient Information leaflet Patient Information leaflet Latvian 27-11-2017
Public Assessment Report Public Assessment Report Latvian 24-02-2021
Patient Information leaflet Patient Information leaflet Lithuanian 27-11-2017
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-11-2017
Public Assessment Report Public Assessment Report Lithuanian 18-07-2007
Patient Information leaflet Patient Information leaflet Hungarian 27-11-2017
Summary of Product characteristics Summary of Product characteristics Hungarian 27-11-2017
Public Assessment Report Public Assessment Report Hungarian 18-07-2007
Patient Information leaflet Patient Information leaflet Maltese 27-11-2017
Public Assessment Report Public Assessment Report Maltese 24-02-2021
Patient Information leaflet Patient Information leaflet Dutch 27-11-2017
Public Assessment Report Public Assessment Report Dutch 24-02-2021
Patient Information leaflet Patient Information leaflet Polish 27-11-2017
Public Assessment Report Public Assessment Report Polish 24-02-2021
Patient Information leaflet Patient Information leaflet Portuguese 27-11-2017
Summary of Product characteristics Summary of Product characteristics Portuguese 27-11-2017
Public Assessment Report Public Assessment Report Portuguese 24-02-2021
Patient Information leaflet Patient Information leaflet Romanian 27-11-2017
Public Assessment Report Public Assessment Report Romanian 24-02-2021
Patient Information leaflet Patient Information leaflet Slovak 27-11-2017
Public Assessment Report Public Assessment Report Slovak 24-02-2021
Patient Information leaflet Patient Information leaflet Finnish 27-11-2017
Public Assessment Report Public Assessment Report Finnish 24-02-2021
Patient Information leaflet Patient Information leaflet Swedish 27-11-2017
Public Assessment Report Public Assessment Report Swedish 24-02-2021
Patient Information leaflet Patient Information leaflet Norwegian 27-11-2017
Summary of Product characteristics Summary of Product characteristics Norwegian 27-11-2017
Patient Information leaflet Patient Information leaflet Icelandic 27-11-2017
Summary of Product characteristics Summary of Product characteristics Icelandic 27-11-2017
Patient Information leaflet Patient Information leaflet Croatian 27-11-2017
Public Assessment Report Public Assessment Report Croatian 24-02-2021

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