Zoledronic acid medac

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

monohidrat zoledronske kiseline

Available from:

medac Gesellschaft für klinische Spezialpräparate mbH

ATC code:

M05BA08

INN (International Name):

zoledronic acid

Therapeutic group:

Lijekovi za liječenje bolesti kostiju

Therapeutic area:

Fractures, Bone; Cancer

Therapeutic indications:

Sprječavanje koštanih vezane uz događaje (patološki prijelomi, spinalne kompresije, zračenja ili operacije kosti ili hiperkalcijemije) u odraslih bolesnika s uznapredovalim zloćudnim bolestima koje uključuju kosti. Liječenje odraslih bolesnika s tumorom-induced гиперкальциемии (TPU).

Product summary:

Revision: 13

Authorization status:

odobren

Authorization date:

2012-08-03

Patient Information leaflet

                                33
B. UPUTA O LIJEKU
34
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
ZOLEDRONATNA KISELINA MEDAC 4 MG/100 ML OTOPINA ZA INFUZIJU
zoledronatna kiselina
PAŽLJIVO PROČITAJTE CIJELU UPUTU PRIJE NEGO PRIMITE OVAJ LIJEK JER
SADRŽI VAMA VAŽNE PODATKE.
-
Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.
-
Ako imate dodatnih pitanja, obratite se liječniku, ljekarniku ili
medicinskoj sestri.
-
Ako primijetite bilo koju nuspojavu, potrebno je obavijestiti
liječnika, ljekarnika ili medicinsku
sestru. To uključuje i svaku moguću nuspojavu koja nije navedena u
ovoj uputi. Pogledajte
dio 4.
ŠTO SE NALAZI U OVOJ UPUTI
1.
Što je Zoledronatna kiselina medac i za što se koristi
2.
Što morate znati prije nego primite Zoledronatnu kiselinu medac
3.
Kako primjenjivati Zoledronatnu kiselinu medac
4.
Moguće nuspojave
5.
Kako čuvati Zoledronatnu kiselinu medac
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE ZOLEDRONATNA KISELINA MEDAC I ZA ŠTO SE KORISTI
Djelatna tvar u Zoledronatnoj kiselini medac je zoledronatna kiselina,
koja pripada skupini tvari koje
se zovu bisfosfonati. Zoledronatna kiselina djeluje tako što se spaja
na kost i usporava brzinu
pregradnje kosti. Koristi se za:
-
SPRJEČAVANJE KOŠTANIH KOMPLIKACIJA
, npr. prijeloma, u odraslih bolesnika s koštanim
metastazama
(širenje raka iz primarnog mjesta u kosti).
-
SMANJENJE KOLIČINE KALCIJA
u krvi u odraslih bolesnika kad je količina kalcija prevelika zbog
prisutnosti tumora. Tumori mogu ubrzati normalnu pregradnju kosti,
zbog čega se kalcij
pojačano otpušta iz kostiju. To se stanje zove hiperkalcemija
izazvana tumorom.
2.
ŠTO MORATE ZNATI PRIJE NEGO PRIMITE ZOLEDRONATNU KISELINU MEDAC
Pažljivo slijedite sve upute koje ste dobili od liječnika.
Prije nego što počnete primati Zoledronatnu kiselinu medac,
liječnik će Vam napraviti krvne pretrage i
u redovitim vremenskim razmacima provjeravati Vaš odgovor na
liječenje.
NE SMIJETE DOBITI ZOLEDRONATNU KISELINU MEDAC
-
ako dojite.
-
ako ste alergični (preosjetljivi) na zoledronatnu k
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Zoledronatna kiselina medac 4 mg/100 ml otopina za infuziju
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Jedna boca sa 100 ml otopine sadrži 4 mg zoledronatne kiseline (u
obliku hidrata).
Jedan ml otopine sadrži 0,04 mg zoledronatne kiseline (u obliku
hidrata).
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Otopina za infuziju.
Bistra, bezbojna otopina.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
-
Sprječavanje koštanih događaja (patološki prijelomi, kompresija
kralježaka, zračenje ili
kirurški zahvat na kosti ili hiperkalcemija izazvana tumorom) u
odraslih bolesnika s
uznapredovalom zloćudnom bolešću koja je zahvatila kosti.
-
Liječenje odraslih bolesnika s hiperkalcemijom izazvanom tumorom.
4.2
DOZIRANJE I NAČIN PRIMJENE
Zoledronatnu kiselinu medac bolesnicima smiju propisivati i
primjenjivati samo liječnici s iskustvom
u intravenskoj primjeni bisfosfonata. Bolesnicima liječenima
Zoledronatnom kiselinom medac treba
dati Uputu o lijeku i karticu s podsjetnikom za bolesnika.
Doziranje
_Sprječavanje koštanih događaja u bolesnika s uznapredovalom
zloćudnom bolešću koja je zahvatila _
_kosti _
_Odrasli i starije osobe _
Preporučena doza za sprječavanje koštanih događaja u bolesnika s
uznapredovalom zloćudnom
bolešću koja je zahvatila kosti iznosi 4 mg zoledronatne kiseline
svaka 3 do 4 tjedna.
Bolesnicima također treba davati peroralni dodatak kalcija od 500 mg
i 400 IU vitamina D na dan.
Pri donošenju odluke da se liječe bolesnici s koštanim metastazama
radi sprječavanja koštanih
događaja treba uzeti u obzir da učinak liječenja nastupa nakon 2 -
3 mjeseca.
_Liječenje hiperkalcemije izazvane tumorom _
_Odrasli i starije osobe _
Preporučena doza kod hiperkalcemije (serumski kalcij korigiran za
albumin ≥ 12,0 mg/dl ili
3,0 mmol/l) je jednokratna doza od 4 mg zoledronatne kiseline.
3
_Oštećenje funkcije bubrega _
_Hiperkalcemija izazvana tumorom: _
Liječenje bolesnika s hiperkalcemijom izazv
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 20-11-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 20-11-2020
Public Assessment Report Public Assessment Report Bulgarian 27-11-2015
Patient Information leaflet Patient Information leaflet Spanish 20-11-2020
Public Assessment Report Public Assessment Report Spanish 27-11-2015
Patient Information leaflet Patient Information leaflet Czech 20-11-2020
Public Assessment Report Public Assessment Report Czech 27-11-2015
Patient Information leaflet Patient Information leaflet Danish 20-11-2020
Public Assessment Report Public Assessment Report Danish 27-11-2015
Patient Information leaflet Patient Information leaflet German 20-11-2020
Public Assessment Report Public Assessment Report German 27-11-2015
Patient Information leaflet Patient Information leaflet Estonian 20-11-2020
Public Assessment Report Public Assessment Report Estonian 27-11-2015
Patient Information leaflet Patient Information leaflet Greek 20-11-2020
Public Assessment Report Public Assessment Report Greek 27-11-2015
Patient Information leaflet Patient Information leaflet English 20-11-2020
Public Assessment Report Public Assessment Report English 27-11-2015
Patient Information leaflet Patient Information leaflet French 20-11-2020
Public Assessment Report Public Assessment Report French 27-11-2015
Patient Information leaflet Patient Information leaflet Italian 20-11-2020
Public Assessment Report Public Assessment Report Italian 27-11-2015
Patient Information leaflet Patient Information leaflet Latvian 20-11-2020
Public Assessment Report Public Assessment Report Latvian 27-11-2015
Patient Information leaflet Patient Information leaflet Lithuanian 20-11-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 20-11-2020
Public Assessment Report Public Assessment Report Lithuanian 27-11-2015
Patient Information leaflet Patient Information leaflet Hungarian 20-11-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 20-11-2020
Public Assessment Report Public Assessment Report Hungarian 27-11-2015
Patient Information leaflet Patient Information leaflet Maltese 20-11-2020
Public Assessment Report Public Assessment Report Maltese 27-11-2015
Patient Information leaflet Patient Information leaflet Dutch 20-11-2020
Public Assessment Report Public Assessment Report Dutch 27-11-2015
Patient Information leaflet Patient Information leaflet Polish 20-11-2020
Public Assessment Report Public Assessment Report Polish 27-11-2015
Patient Information leaflet Patient Information leaflet Portuguese 20-11-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 20-11-2020
Public Assessment Report Public Assessment Report Portuguese 27-11-2015
Patient Information leaflet Patient Information leaflet Romanian 20-11-2020
Public Assessment Report Public Assessment Report Romanian 27-11-2015
Patient Information leaflet Patient Information leaflet Slovak 20-11-2020
Public Assessment Report Public Assessment Report Slovak 27-11-2015
Patient Information leaflet Patient Information leaflet Slovenian 20-11-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 20-11-2020
Public Assessment Report Public Assessment Report Slovenian 27-11-2015
Patient Information leaflet Patient Information leaflet Finnish 20-11-2020
Public Assessment Report Public Assessment Report Finnish 27-11-2015
Patient Information leaflet Patient Information leaflet Swedish 20-11-2020
Public Assessment Report Public Assessment Report Swedish 27-11-2015
Patient Information leaflet Patient Information leaflet Norwegian 20-11-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 20-11-2020
Patient Information leaflet Patient Information leaflet Icelandic 20-11-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 20-11-2020