ViraferonPeg

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

пэгинтерферон Alfa-2B

Available from:

Merck Sharp Dohme Ltd 

ATC code:

L03AB10

INN (International Name):

peginterferon alfa-2b

Therapeutic group:

Иммуностимуляторы,

Therapeutic area:

Hepatitis C, kronični

Therapeutic indications:

Adults (tritherapy)ViraferonPeg in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-C (CHC) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. Molimo vas, obratite se Ribavirin i боцепревир kratke specifikacije robe (SmPCs), kada ViraferonPeg se koristi u kombinaciji s ovi lijekovi. Adults (bitherapy and monotherapy)ViraferonPeg is indicated for the treatment of adult patients (18 years of age and older) with CHC who are positive for hepatitis-C-virus RNA (HCV-RNA), including patients with compensated cirrhosis and / or co-infected with clinically stable HIV. ViraferonPeg u kombinaciji s ribavirinom (bitherapy) indiciran za liječenje ХГС-infekcije kod odraslih pacijenata koji nisu prethodno tretirani tretman, uključujući i bolesnike s klinički stabilan HIV-infekcije i kod odraslih pacijenata koji nisu prethodno liječenje interferonom Alfa (пегилированным ili пегилированным) i ribavirinom kombinirana terapija ili монотерапия interferonom Alfa. Монотерапия interferonom, uključujući ViraferonPeg, navedeno je u slučaju netolerancije ili kontraindikacija za рибавирину. Molimo vas, obratite se Смпц ribavirinom, kada ViraferonPeg se koristi u kombinaciji s ribavirinom. Paediatric population (bitherapy)ViraferonPeg is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents, who have chronic hepatitis C, previously untreated, without liver decompensation, and who are positive for HCV-RNA. Donošenju odluke da se neće odgoditi liječenje do odrasle dobi, važno je uzeti u obzir da je kombinirana terapija uzrokuje zadržavanje rasta, koji može biti nepovratan u nekih bolesnika. Odluka mora biti donesena na individualnoj osnovi. Molimo vas, obratite se Смпц Ribavirin kapsule ili usmeno rješenje, kada ViraferonPeg se koristi u kombinaciji s ribavirinom.

Product summary:

Revision: 36

Authorization status:

povučen

Authorization date:

2000-05-28

Patient Information leaflet

                                114
B. UPUTA O LIJEKU
115
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
VIRAFERONPEG 50 MIKROGRAMA PRAŠAK I OTAPALO ZA OTOPINU ZA INJEKCIJU
VIRAFERONPEG 80 MIKROGRAMA PRAŠAK I OTAPALO ZA OTOPINU ZA INJEKCIJU
VIRAFERONPEG 100 MIKROGRAMA PRAŠAK I OTAPALO ZA OTOPINU ZA INJEKCIJU
VIRAFERONPEG 120 MIKROGRAMA PRAŠAK I OTAPALO ZA OTOPINU ZA INJEKCIJU
VIRAFERONPEG 150 MIKROGRAMA PRAŠAK I OTAPALO ZA OTOPINU ZA INJEKCIJU
peginterferon alfa-2b
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 ViraferonPeg i za što se koristi
2.
Što morate znati prije nego počnete primjenjivati ViraferonPeg
3.
Kako primjenjivati ViraferonPeg
4.
Moguće nuspojave
5.
Kako čuvati ViraferonPeg
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE VIRAFERONPEG I ZA ŠTO SE KORISTI
Djelatna tvar u ovom lijeku je protein peginterferon alfa-2b, koji
pripada skupini lijekova koji se
nazivaju interferoni. Interferone proizvodi Vaš imunološki sustav
kako bi pomogli u borbi protiv
infekcija i teških bolesti. Ovaj lijek se injicira u tijelo kako bi
djelovao na imunološki sustav. Ovaj
lijek se koristi za liječenje kroničnog hepatitisa C, virusne
infekcije jetre.
Odrasli
Kombinacija ovog lijeka, ribavirina i boceprevira preporučuje se za
liječenje nekih vrsta kronične
infekcije virusom hepatitisa C (naziva se i HCV infekcijom) u odraslih
osoba u dobi od 18 i više
godina. Može se koristiti u odraslih koji prethodno nisu liječili
HCV infekciju ili koji su ranije koristili
lijekove koji se zovu inter
                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
ViraferonPeg 50 mikrograma prašak i otapalo za otopinu za injekciju
ViraferonPeg 80 mikrograma prašak i otapalo za otopinu za injekciju
ViraferonPeg 100 mikrograma prašak i otapalo za otopinu za injekciju
ViraferonPeg 120 mikrograma prašak i otapalo za otopinu za injekciju
ViraferonPeg 150 mikrograma prašak i otapalo za otopinu za injekciju
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
ViraferonPeg 50 mikrograma prašak i otapalo za otopinu za injekciju
Jedna bočica sadrži 50 mikrograma peginterferona alfa-2b, mjereno na
bazi proteina.
Kada se rekonstituira prema uputama, iz jedne se bočice dobije 50
mikrograma/0,5 ml peginterferona
alfa-2b.
ViraferonPeg 80 mikrograma prašak i otapalo za otopinu za injekciju
Jedna bočica sadrži 80 mikrograma peginterferona alfa-2b, mjereno na
bazi proteina.
Kada se rekonstituira prema uputama, iz jedne se bočice dobije 80
mikrograma/0,5 ml peginterferona
alfa-2b.
ViraferonPeg 100 mikrograma prašak i otapalo za otopinu za injekciju
Jedna bočica sadrži 100 mikrograma peginterferona alfa-2b, mjereno
na bazi proteina.
Kada se rekonstituira prema uputama, iz jedne se bočice dobije 100
mikrograma/0,5 ml peginterferona
alfa-2b.
ViraferonPeg 120 mikrograma prašak i otapalo za otopinu za injekciju
Jedna bočica sadrži 120 mikrograma peginterferona alfa-2b, mjereno
na bazi proteina.
Kada se rekonstituira prema uputama, iz jedne se bočice dobije 120
mikrograma/0,5 ml peginterferona
alfa-2b.
ViraferonPeg 150 mikrograma prašak i otapalo za otopinu za injekciju
Jedna bočica sadrži 150 mikrograma peginterferona alfa-2b, mjereno
na bazi proteina.
Kada se rekonstituira prema uputama, iz jedne se bočice dobije 150
mikrograma/0,5 ml peginterferona
alfa-2b.
Djelatna tvar je kovalentni konjugat rekombinantnog interferona
alfa-2b* s
monometoksipolietilenglikolom. Jačina ovog lijeka ne smije se
uspoređivati s jačinom drugih
pegiliranih ili nepegiliranih proteina iz istog terapijskog razreda
(vidjeti dio 5.1).
*proizvedenog
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 22-01-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 22-01-2021
Public Assessment Report Public Assessment Report Bulgarian 22-01-2021
Patient Information leaflet Patient Information leaflet Spanish 22-01-2021
Public Assessment Report Public Assessment Report Spanish 22-01-2021
Patient Information leaflet Patient Information leaflet Czech 22-01-2021
Public Assessment Report Public Assessment Report Czech 22-01-2021
Patient Information leaflet Patient Information leaflet Danish 22-01-2021
Public Assessment Report Public Assessment Report Danish 22-01-2021
Patient Information leaflet Patient Information leaflet German 22-01-2021
Public Assessment Report Public Assessment Report German 22-01-2021
Patient Information leaflet Patient Information leaflet Estonian 22-01-2021
Public Assessment Report Public Assessment Report Estonian 22-01-2021
Patient Information leaflet Patient Information leaflet Greek 22-01-2021
Public Assessment Report Public Assessment Report Greek 22-01-2021
Patient Information leaflet Patient Information leaflet English 22-01-2021
Public Assessment Report Public Assessment Report English 22-01-2021
Patient Information leaflet Patient Information leaflet French 22-01-2021
Public Assessment Report Public Assessment Report French 22-01-2021
Patient Information leaflet Patient Information leaflet Italian 22-01-2021
Public Assessment Report Public Assessment Report Italian 22-01-2021
Patient Information leaflet Patient Information leaflet Latvian 22-01-2021
Public Assessment Report Public Assessment Report Latvian 22-01-2021
Patient Information leaflet Patient Information leaflet Lithuanian 22-01-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 22-01-2021
Public Assessment Report Public Assessment Report Lithuanian 22-01-2021
Patient Information leaflet Patient Information leaflet Hungarian 22-01-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 22-01-2021
Public Assessment Report Public Assessment Report Hungarian 22-01-2021
Patient Information leaflet Patient Information leaflet Maltese 22-01-2021
Public Assessment Report Public Assessment Report Maltese 22-01-2021
Patient Information leaflet Patient Information leaflet Dutch 22-01-2021
Public Assessment Report Public Assessment Report Dutch 22-01-2021
Patient Information leaflet Patient Information leaflet Polish 22-01-2021
Public Assessment Report Public Assessment Report Polish 22-01-2021
Patient Information leaflet Patient Information leaflet Portuguese 22-01-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 22-01-2021
Public Assessment Report Public Assessment Report Portuguese 22-01-2021
Patient Information leaflet Patient Information leaflet Romanian 22-01-2021
Public Assessment Report Public Assessment Report Romanian 22-01-2021
Patient Information leaflet Patient Information leaflet Slovak 22-01-2021
Public Assessment Report Public Assessment Report Slovak 22-01-2021
Patient Information leaflet Patient Information leaflet Slovenian 22-01-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 22-01-2021
Public Assessment Report Public Assessment Report Slovenian 22-01-2021
Patient Information leaflet Patient Information leaflet Finnish 22-01-2021
Public Assessment Report Public Assessment Report Finnish 22-01-2021
Patient Information leaflet Patient Information leaflet Swedish 22-01-2021
Public Assessment Report Public Assessment Report Swedish 22-01-2021
Patient Information leaflet Patient Information leaflet Norwegian 22-01-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 22-01-2021
Patient Information leaflet Patient Information leaflet Icelandic 22-01-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 22-01-2021

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