Urorec

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

silodosin

Available from:

Recordati Ireland Ltd

ATC code:

G04CA04

INN (International Name):

silodosin

Therapeutic group:

Urologicals

Therapeutic area:

Prostata Hyperplasia

Therapeutic indications:

Liječenje znakova i simptoma benigne hiperplazije prostate (BPH).

Product summary:

Revision: 18

Authorization status:

odobren

Authorization date:

2010-01-29

Patient Information leaflet

                                24
B. UPUTA O LIJEKU
25
UPUTA O LIJEKU: INFORMACIJE ZA BOLESNIKA
_ _
UROREC 8 MG TVRDE KAPSULE
UROREC 4 MG TVRDE KAPSULE
silodozin
PAŽLJIVO PROČITAJTE CIJELU UPUTU PRIJE NEGO POČNETE PRIMJENJIVATI
OVAJ LIJEK JER SADRŽI VAMA
VAŽNE PODATKE.
-
Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.
-
Ako imate dodatnih pitanja, obratite se svom liječniku ili
ljekarniku.
-
Ovaj je lijek propisan samo Vama. Nemojte ga davati drugima. Može im
naškoditi, čak i ako su
njihovi znakovi bolesti jednaki Vašima.
-
Ako primijetite bilo koju nuspojavu, potrebno je obavijestiti
liječnika ili ljekarnika. To uključuje
i svaku moguću nuspojavu koja nije navedena u ovoj uputi. Pogledajte
dio 4.
_ _
ŠTO SE NALAZI U OVOJ UPUTI:
1.
Što je Urorec i za što se koristi
2.
Što morate znati prije nego počnete uzimati Urorec
3.
Kako uzimati Urorec
4.
Moguće nuspojave
5.
Kako čuvati Urorec
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE UROREC I ZA ŠTO SE KORISTI
ŠTO JE UROREC
Urorec pripada skupini lijekova koji se zovu blokatori alfa
1A
-adrenergičkih receptora.
Urorec se selektivno veže za receptore koji se nalaze u prostati,
mokraćnom mjehuru i mokraćnoj
cijevi. Blokiranjem ovih receptora, Urorec uzrokuje opuštanje glatkih
mišića u tim tkivima. To
olakšava mokrenje i ublažava simptome.
ZA ŠTO SE UROREC KORISTI
Urorec se primjenjuje u odraslih muškaraca za liječenje urinarnih
simptoma povezanih s dobroćudnim
povećanjem prostate (hiperplazija prostate), kao što su:
•
otežan početak mokrenja,
•
osjećaj nepotpunog pražnjenja mokraćnog mjehura,
•
učestala potreba za mokrenjem, čak i noću.
2.
ŠTO MORATE ZNATI PRIJE NEGO POČNETE UZIMATI UROREC
_ _
NEMOJTE UZIMATI
UROREC
ako ste alergični na silodozin ili neki drugi sastojak ovog lijeka
(naveden u dijelu 6).
26
UPOZORENJA I MJERE OPREZA
Obratite se svom liječniku ili ljekarniku prije nego uzmete Urorec.
•
Ako idete na operaciju oka zbog zamućenja leće (
OPERACIJA KATARAKTE
), važno je da odmah
obavijestite svog specijalistu
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Urorec 4 mg tvrde kapsule
Urorec 8 mg tvrde kapsule
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Urorec 4 mg tvrde kapsule
Jedna tvrda kapsula sadrži 4 mg silodozina.
Urorec 8 mg tvrde kapsule
Jedna tvrda kapsula sadrži 8 mg silodozina
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Tvrda kapsula.
Urorec 4 mg tvrde kapsule
Žuta, neprozirna, tvrda želatinska kapsula, veličine 3 (približno
15,9 x 5,8 mm).
Urorec 8 mg tvrde kapsule
Bijela, neprozirna, tvrda želatinska kapsula, veličine 0 (približno
21,7 x 7,6 mm).
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Liječenje znakova i simptoma benigne hiperplazije prostate (BHP) u
odraslih muškaraca.
4.2
DOZIRANJE I NAČIN PRIMJENE
Doziranje
Preporučena doza je jedna kapsula lijeka Urorec 8 mg na dan. Kod
posebnih populacija bolesnika,
preporučuje se jedna kapsula lijeka Urorec 4 mg na dan (vidjeti
niže).
_Starije osobe _
Nije potrebna prilagodba doze u starijih osoba (vidjeti dio 5.2).
_Oštećenje funkcije bubrega _
Nije potrebna prilagodba doze u bolesnika s blagim oštećenjem
funkcije bubrega (CL
cr
≥ 50
do ≤ 80 ml/min).
U bolesnika s umjerenim oštećenjem bubrega (CL
cr
≥ 30 do < 50 ml/min) preporučuje se početna doza
od 4 mg jedanput na dan, koja se može povećati na 8 mg jedanput na
dan nakon jednog tjedna
liječenja, ovisno o odgovoru pojedinog bolesnika. Ne preporučuje se
primjena u bolesnika s teškim
oštećenjem funkcije bubrega (CL
cr
<30 ml/min) (vidjeti dijelove 4.4 i 5.2).
_Oštećenje funkcije jetre _
Nije potrebna prilagodba doze kod bolesnika s blagim do umjerenim
oštećenjem funkcije jetre.
Kako nema dostupnih podataka, ne preporučuje se primjena u bolesnika
s teškim oštećenjem funkcije
jetre (vidjeti dijelove 4.4 i 5.2).
3
_Pedijatrijska populacija _
Nema relevantne primjene lijeka Urorec u pedijatrijskoj populaciji za
indikaciju benigne hiperplazije
prostate (BPH).
Način primjene
Peroralna primjena.
Kapsulu je potrebno uzeti s hranom, po 
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 06-04-2022
Public Assessment Report Public Assessment Report Bulgarian 08-10-2014
Patient Information leaflet Patient Information leaflet Spanish 06-04-2022
Public Assessment Report Public Assessment Report Spanish 08-10-2014
Patient Information leaflet Patient Information leaflet Czech 06-04-2022
Public Assessment Report Public Assessment Report Czech 08-10-2014
Patient Information leaflet Patient Information leaflet Danish 06-04-2022
Public Assessment Report Public Assessment Report Danish 08-10-2014
Patient Information leaflet Patient Information leaflet German 06-04-2022
Public Assessment Report Public Assessment Report German 08-10-2014
Patient Information leaflet Patient Information leaflet Estonian 06-04-2022
Public Assessment Report Public Assessment Report Estonian 08-10-2014
Patient Information leaflet Patient Information leaflet Greek 06-04-2022
Public Assessment Report Public Assessment Report Greek 08-10-2014
Patient Information leaflet Patient Information leaflet English 06-04-2022
Public Assessment Report Public Assessment Report English 08-10-2014
Patient Information leaflet Patient Information leaflet French 06-04-2022
Public Assessment Report Public Assessment Report French 08-10-2014
Patient Information leaflet Patient Information leaflet Italian 06-04-2022
Public Assessment Report Public Assessment Report Italian 08-10-2014
Patient Information leaflet Patient Information leaflet Latvian 06-04-2022
Public Assessment Report Public Assessment Report Latvian 08-10-2014
Patient Information leaflet Patient Information leaflet Lithuanian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 06-04-2022
Public Assessment Report Public Assessment Report Lithuanian 08-10-2014
Patient Information leaflet Patient Information leaflet Hungarian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 06-04-2022
Public Assessment Report Public Assessment Report Hungarian 08-10-2014
Patient Information leaflet Patient Information leaflet Maltese 06-04-2022
Public Assessment Report Public Assessment Report Maltese 08-10-2014
Patient Information leaflet Patient Information leaflet Dutch 06-04-2022
Public Assessment Report Public Assessment Report Dutch 08-10-2014
Patient Information leaflet Patient Information leaflet Polish 06-04-2022
Public Assessment Report Public Assessment Report Polish 08-10-2014
Patient Information leaflet Patient Information leaflet Portuguese 06-04-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 06-04-2022
Public Assessment Report Public Assessment Report Portuguese 08-10-2014
Patient Information leaflet Patient Information leaflet Romanian 06-04-2022
Public Assessment Report Public Assessment Report Romanian 08-10-2014
Patient Information leaflet Patient Information leaflet Slovak 06-04-2022
Public Assessment Report Public Assessment Report Slovak 08-10-2014
Patient Information leaflet Patient Information leaflet Slovenian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 06-04-2022
Public Assessment Report Public Assessment Report Slovenian 08-10-2014
Patient Information leaflet Patient Information leaflet Finnish 06-04-2022
Public Assessment Report Public Assessment Report Finnish 08-10-2014
Patient Information leaflet Patient Information leaflet Swedish 06-04-2022
Public Assessment Report Public Assessment Report Swedish 08-10-2014
Patient Information leaflet Patient Information leaflet Norwegian 06-04-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 06-04-2022
Patient Information leaflet Patient Information leaflet Icelandic 06-04-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 06-04-2022

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