Harvoni

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

ледипасвир, софосбувир

Available from:

Gilead Sciences Ireland UC

ATC code:

J05AX65

INN (International Name):

ledispavir, sofosbuvir

Therapeutic group:

Antivirusni lijekovi za sustavnu uporabu

Therapeutic area:

Hepatitis C, kronični

Therapeutic indications:

Harvoni is indicated for the treatment of chronic hepatitis C (CHC) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 i 5. Virus hepatitisa C (HCV) genotip-specifične aktivnosti vidi 4. 4 i 5.

Product summary:

Revision: 28

Authorization status:

odobren

Authorization date:

2014-11-17

Patient Information leaflet

                                95
B. UPUTA O LIJEKU
96
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
HARVONI 90 MG/400 MG FILMOM OBLOŽENE TABLETE
HARVONI 45 MG/200 MG FILMOM OBLOŽENE TABLETE
ledipasvir/sofosbuvir
PAŽLJIVO PROČITAJTE CIJELU UPUTU PRIJE NEGO POČNETE UZIMATI OVAJ
LIJEK JER SADRŽI VAMA VAŽNE
PODATKE.
-
Sačuvajte ovu uputu. Možda ćete je trebati ponovno pročitati.
-
Ako imate dodatnih pitanja, obratite se 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 Harvoni i za što se koristi
2.
Što morate znati prije nego počnete uzimati Harvoni
3.
Kako uzimati Harvoni
4.
Moguće nuspojave
5.
Kako čuvati Harvoni
6.
Sadržaj pakiranja i druge informacije
AKO JE LIJEK HARVONI PROPISAN VAŠEM DJETETU, TADA SE SVE INFORMACIJE
NAVEDENE U OVOJ UPUTI
ODNOSE NA VAŠE DIJETE (U TOM SLUČAJU ČITAJTE „VAŠE DIJETE“
UMJESTO „VI“)
1.
ŠTO JE HARVONI I ZA ŠTO SE KORISTI
Harvoni je lijek koji sadrži djelatne tvari ledipasvir i sofosbuvir.
Harvoni se koristi za liječenje
kronične (dugotrajne) infekcije virusom hepatitisa C u
ODRASLIH
i DJECE U DOBI OD 3 I VIŠE GODINA
.
Hepatitis C je virusna infekcija jetre. Djelatne tvari u ovom lijeku
djeluju zajedno tako što blokiraju
dva različita proteina koja su virusu potrebna za rast i umnažanje i
time omogućuju trajno uklanjanje
infekcije iz tijela.
Harvoni se ponekad uzima s drugim lijekom, ribavirinom.
Vrlo je važno da pročitate i upute o lijeku za druge lijekove koje
ćete uzimati s lijekom Harvoni. Ako
imate bilo kakvih pitanja o ovim lijekovima, obratite se svom
liječniku ili ljekarniku.
2.
ŠTO MORATE ZNATI PRIJE NEGO POČNETE UZIMATI HARVONI
NEMOJTE UZIMATI HARVONI
•
AKO STE ALERGIČNI
na ledipasvir, sofosbuvir ili neki drugi sastojak ovog lije
                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Harvoni 90 mg/400 mg filmom obložene tablete
Harvoni 45 mg/200 mg filmom obložene tablete
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Harvoni 90 mg/400 mg filmom obložene tablete
Jedna filmom obložena tableta sadrži 90 mg ledipasvira i 400 mg
sofosbuvira.
Pomoćne tvari s poznatim učinkom
Jedna filmom obložena tableta sadrži 157 mg laktoze (u obliku
laktoze hidrata) i 47 mikrograma boje
_sunset yellow FCF_
.
Harvoni 45 mg/200 mg filmom obložene tablete
Jedna filmom obložena tableta sadrži 45 mg ledipasvira i 200 mg
sofosbuvira.
Pomoćne tvari s poznatim učinkom
Jedna filmom obložena tableta sadrži 78 mg laktoze (u obliku laktoze
hidrata).
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Filmom obložena tableta.
Harvoni 90 mg/400 mg filmom obložene tablete
Narančasta, filmom obložena tableta u obliku romba, veličine
otprilike 19 mm x 10 mm, s utisnutim
“GSI” na jednoj strani i “7985” na drugoj strani.
Harvoni 45 mg/200 mg filmom obložene tablete
Bijela, filmom obložena tableta u obliku kapsule, veličine otprilike
14 mm x 7 mm, s utisnutim “GSI”
na jednoj strani i “HRV” na drugoj strani.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Harvoni je indiciran za liječenje kroničnog hepatitisa C (CHC) u
odraslih i pedijatrijskih bolesnika u
dobi od 3 godine i više (vidjeti dijelove 4.2, 4.4 i 5.1).
Za djelovanje na određeni genotip virusa hepatitisa C (HCV), vidjeti
dijelove 4.4 i 5.1.
4.2
DOZIRANJE I NAČIN PRIMJENE
Liječenje lijekom Harvoni treba započeti i nadzirati liječnik s
iskustvom u liječenju bolesnika s
CHC-om.
3
Doziranje
Preporučena doza lijeka Harvoni u odraslih osoba je 90 mg/400 mg
jedanput na dan s hranom ili bez
nje (vidjeti dio 5.2).
Preporučena doza lijeka Harvoni u pedijatrijskih bolesnika u dobi od
3 godine i više temelji se na
težini (kako je navedeno u Tablici 2), a može se uzimati s hranom
ili bez hrane (vidjeti dio 5.2).
Formulacija lijeka Harvoni u obliku granula do
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 10-11-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 10-11-2022
Public Assessment Report Public Assessment Report Bulgarian 29-07-2020
Patient Information leaflet Patient Information leaflet Spanish 10-11-2022
Public Assessment Report Public Assessment Report Spanish 29-07-2020
Patient Information leaflet Patient Information leaflet Czech 10-11-2022
Public Assessment Report Public Assessment Report Czech 29-07-2020
Patient Information leaflet Patient Information leaflet Danish 10-11-2022
Public Assessment Report Public Assessment Report Danish 29-07-2020
Patient Information leaflet Patient Information leaflet German 10-11-2022
Public Assessment Report Public Assessment Report German 29-07-2020
Patient Information leaflet Patient Information leaflet Estonian 10-11-2022
Public Assessment Report Public Assessment Report Estonian 29-07-2020
Patient Information leaflet Patient Information leaflet Greek 10-11-2022
Public Assessment Report Public Assessment Report Greek 29-07-2020
Patient Information leaflet Patient Information leaflet English 10-11-2022
Public Assessment Report Public Assessment Report English 29-07-2020
Patient Information leaflet Patient Information leaflet French 10-11-2022
Public Assessment Report Public Assessment Report French 29-07-2020
Patient Information leaflet Patient Information leaflet Italian 10-11-2022
Public Assessment Report Public Assessment Report Italian 29-07-2020
Patient Information leaflet Patient Information leaflet Latvian 10-11-2022
Public Assessment Report Public Assessment Report Latvian 29-07-2020
Patient Information leaflet Patient Information leaflet Lithuanian 10-11-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 10-11-2022
Public Assessment Report Public Assessment Report Lithuanian 29-07-2020
Patient Information leaflet Patient Information leaflet Hungarian 10-11-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 10-11-2022
Public Assessment Report Public Assessment Report Hungarian 29-07-2020
Patient Information leaflet Patient Information leaflet Maltese 10-11-2022
Public Assessment Report Public Assessment Report Maltese 29-07-2020
Patient Information leaflet Patient Information leaflet Dutch 10-11-2022
Public Assessment Report Public Assessment Report Dutch 29-07-2020
Patient Information leaflet Patient Information leaflet Polish 10-11-2022
Public Assessment Report Public Assessment Report Polish 29-07-2020
Patient Information leaflet Patient Information leaflet Portuguese 10-11-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 10-11-2022
Public Assessment Report Public Assessment Report Portuguese 29-07-2020
Patient Information leaflet Patient Information leaflet Romanian 10-11-2022
Public Assessment Report Public Assessment Report Romanian 29-07-2020
Patient Information leaflet Patient Information leaflet Slovak 10-11-2022
Public Assessment Report Public Assessment Report Slovak 29-07-2020
Patient Information leaflet Patient Information leaflet Slovenian 10-11-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 10-11-2022
Public Assessment Report Public Assessment Report Slovenian 29-07-2020
Patient Information leaflet Patient Information leaflet Finnish 10-11-2022
Public Assessment Report Public Assessment Report Finnish 29-07-2020
Patient Information leaflet Patient Information leaflet Swedish 10-11-2022
Public Assessment Report Public Assessment Report Swedish 29-07-2020
Patient Information leaflet Patient Information leaflet Norwegian 10-11-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 10-11-2022
Patient Information leaflet Patient Information leaflet Icelandic 10-11-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 10-11-2022

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