Descovy

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

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Active ingredient:

эмтрицитабин, Тенофовир alafenamide

Available from:

Gilead Sciences Ireland UC

ATC code:

J05AR17

INN (International Name):

emtricitabine, tenofovir alafenamide

Therapeutic group:

Antivirusni lijekovi za sustavnu uporabu

Therapeutic area:

HIV infekcije

Therapeutic indications:

Descovy is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (HIV-1).

Product summary:

Revision: 20

Authorization status:

odobren

Authorization date:

2016-04-21

Patient Information leaflet

                                64
B. UPUTA O LIJEKU
65
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
DESCOVY 200 MG/10 MG FILMOM OBLOŽENE TABLETE
emtricitabin/tenofoviralafenamid
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 Descovy i za što se koristi
2.
Što morate znati prije nego počnete uzimati lijek Descovy
3.
Kako uzimati lijek Descovy
4.
Moguće nuspojave
5.
Kako čuvati lijek Descovy
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE DESCOVY I ZA ŠTO SE KORISTI
Descovy sadrži dvije djelatne tvari:
•
EMTRICITABIN
, antiretrovirusni lijek poznat kao nukleozidni inhibitor reverzne
transkriptaze
(NRTI)
•
TENOFOVIRALAFENAMID
, antiretrovirusni lijek poznat kao nukleotidni inhibitor reverzne
transkriptaze (NtRTI).
Descovy koči djelovanje enzima reverzne transkriptaze koji je nužan
za umnažanje virusa. Zato
Descovy smanjuje količinu HIV-a u Vašem tijelu.
Descovy se u kombinaciji s drugim lijekovima primjenjuje za
LIJEČENJE INFEKCIJE VIRUSOM HUMANE
IMUNODEFICIJENCIJE 1 (HIV-1)
u odraslih i adolescenata u dobi od 12 godina i starijih, koji imaju
tjelesnu težinu od najmanje 35 kg.
2.
ŠTO MORATE ZNATI PRIJE NEGO POČNETE UZIMATI LIJEK DESCOVY
NEMOJTE UZIMATI LIJEK DESCOVY
•
AKO STE ALERGIČNI NA EMTRICITABIN, TENOFOVIRALAFENAMID
ili neki drugi sastojak ovog lijeka
(naveden u dijelu 6. ove upute).
UPOZORENJA I MJERE OPREZA
Za vrijeme uzimanja lijeka Descovy morate ostati pod nadzorom svog
liječnika.
Ovaj lijek ne može izliječiti HIV-infekciju. Dok uzimate lijek
Descovy i dalje mo
                                
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Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Descovy 200 mg/10 mg filmom obložene tablete
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Jedna tableta sadrži 200 mg emtricitabina i
tenofoviralafenamidfumarat što odgovara 10 mg
tenofoviralafenamida.
3.
FARMACEUTSKI OBLIK
Filmom obložena tableta.
Siva filmom obložena tableta pravokutnog oblika veličine 12,5 mm x
6,4 mm, s utisnutom oznakom
„GSI“ na jednoj strani i „210“ na drugoj strani tablete.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Lijek Descovy je indiciran u kombinaciji s drugim antiretrovirusnim
lijekovima za liječenje odraslih
osoba i adolescenata (u dobi od 12 godina i starijih, s tjelesnom
težinom od najmanje 35 kg) zaraženih
virusom humane imunodeficijencije tipa 1 (HIV-1) (vidjeti dijelove 4.2
i 5.1).
4.2
DOZIRANJE I NAČIN PRIMJENE
Terapiju mora započeti liječnik s iskustvom u liječenju infekcije
HIV-om.
Doziranje
_ _
Descovy se primjenjuje kako je prikazano u tablici 1.
TABLICA 1: DOZA LIJEKA DESCOVY OVISNO O TREĆEM LIJEKU U REŽIMU
LIJEČENJA HIV-A
DOZA LIJEKA DESCOVY
TREĆI LIJEK U REŽIMU LIJEČENJA HIV-A
(vidjeti dio 4.5)
Descovy 200/10 mg
jedanput na dan
atazanavir s ritonavirom ili kobicistatom
darunavir s ritonavirom ili kobicistatom
1
lopinavir s ritonavirom
Descovy 200/25 mg
jedanput na dan
dolutegravir, efavirenz, maravirok, nevirapin,
rilpivirin, raltegravir
1
U ispitanika koji prethodno nisu bili liječeni ispitivan je lijek
Descovy 200/10 mg primjenjen s fiksnom kombinacijom
800 mg darunavira i 150 mg kobicistata u jednoj tableti (vidjeti dio
5.1).
_Propuštene doze _
Ako je bolesnik propustio uzeti dozu lijeka Descovy, a sjetio se
unutar 18 sati od propuštene doze,
bolesnik mora što prije uzeti lijek Descovy i potom ga nastaviti
uzimati prema uobičajenom rasporedu.
Ako je od propuštene doze prošlo više od 18 sati, bolesnik ne treba
uzeti propuštenu dozu nego
jednostavno nastaviti uzimati doze prema uobičajenom rasporedu.
Ako bolesnik povraća unutar 1 sata od uzimanja lijeka Descovy, mora
uzeti 
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 17-02-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 17-02-2023
Public Assessment Report Public Assessment Report Bulgarian 01-06-2016
Patient Information leaflet Patient Information leaflet Spanish 17-02-2023
Public Assessment Report Public Assessment Report Spanish 01-06-2016
Patient Information leaflet Patient Information leaflet Czech 17-02-2023
Public Assessment Report Public Assessment Report Czech 01-06-2016
Patient Information leaflet Patient Information leaflet Danish 17-02-2023
Public Assessment Report Public Assessment Report Danish 01-06-2016
Patient Information leaflet Patient Information leaflet German 17-02-2023
Public Assessment Report Public Assessment Report German 01-06-2016
Patient Information leaflet Patient Information leaflet Estonian 17-02-2023
Public Assessment Report Public Assessment Report Estonian 01-06-2016
Patient Information leaflet Patient Information leaflet Greek 17-02-2023
Public Assessment Report Public Assessment Report Greek 01-06-2016
Patient Information leaflet Patient Information leaflet English 17-02-2023
Public Assessment Report Public Assessment Report English 01-06-2016
Patient Information leaflet Patient Information leaflet French 17-02-2023
Public Assessment Report Public Assessment Report French 01-06-2016
Patient Information leaflet Patient Information leaflet Italian 17-02-2023
Public Assessment Report Public Assessment Report Italian 01-06-2016
Patient Information leaflet Patient Information leaflet Latvian 17-02-2023
Public Assessment Report Public Assessment Report Latvian 01-06-2016
Patient Information leaflet Patient Information leaflet Lithuanian 17-02-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 17-02-2023
Public Assessment Report Public Assessment Report Lithuanian 01-06-2016
Patient Information leaflet Patient Information leaflet Hungarian 17-02-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 17-02-2023
Public Assessment Report Public Assessment Report Hungarian 01-06-2016
Patient Information leaflet Patient Information leaflet Maltese 17-02-2023
Public Assessment Report Public Assessment Report Maltese 01-06-2016
Patient Information leaflet Patient Information leaflet Dutch 17-02-2023
Public Assessment Report Public Assessment Report Dutch 01-06-2016
Patient Information leaflet Patient Information leaflet Polish 17-02-2023
Public Assessment Report Public Assessment Report Polish 01-06-2016
Patient Information leaflet Patient Information leaflet Portuguese 17-02-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 17-02-2023
Public Assessment Report Public Assessment Report Portuguese 01-06-2016
Patient Information leaflet Patient Information leaflet Romanian 17-02-2023
Public Assessment Report Public Assessment Report Romanian 01-06-2016
Patient Information leaflet Patient Information leaflet Slovak 17-02-2023
Public Assessment Report Public Assessment Report Slovak 01-06-2016
Patient Information leaflet Patient Information leaflet Slovenian 17-02-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 17-02-2023
Public Assessment Report Public Assessment Report Slovenian 01-06-2016
Patient Information leaflet Patient Information leaflet Finnish 17-02-2023
Public Assessment Report Public Assessment Report Finnish 01-06-2016
Patient Information leaflet Patient Information leaflet Swedish 17-02-2023
Public Assessment Report Public Assessment Report Swedish 01-06-2016
Patient Information leaflet Patient Information leaflet Norwegian 17-02-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 17-02-2023
Patient Information leaflet Patient Information leaflet Icelandic 17-02-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 17-02-2023

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