Micardis

Country: European Union

Language: Croatian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Telmisartan

Available from:

Boehringer Ingelheim International GmbH

ATC code:

C09CA07

INN (International Name):

telmisartan

Therapeutic group:

Angiotenzin II antagonisti, obični

Therapeutic area:

Hipertenzija

Therapeutic indications:

HypertensionTreatment эссенциальной hipertenzije u odraslih. Kardiovaskularne preventionReduction kardiovaskularnog morbiditeta kod pacijenata s:manifest атеротромботических kardiovaskularne bolesti (povijest bolesti koronarnih arterija, moždani udar ili periferne vaskularne bolesti) ili dijabetesa tipa 2. tip s задокументированным poraz organa-mete.

Product summary:

Revision: 27

Authorization status:

odobren

Authorization date:

1998-12-16

Patient Information leaflet

                                44
B. UPUTA O LIJEKU
45
UPUTA O LIJEKU: INFORMACIJE ZA KORISNIKA
MICARDIS 20 MG TABLETE
telmisartan
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 Micardis i za što se koristi
2.
Što morate znati prije nego počnete uzimati Micardis
3.
Kako uzimati Micardis
4.
Moguće nuspojave
5.
Kako čuvati Micardis
6.
Sadržaj pakiranja i druge informacije
1.
ŠTO JE MICARDIS I ZA ŠTO SE KORISTI
Micardis pripada skupini lijekova poznatih kao antagonisti receptora
angiotenzina II. Angiotenzin II je
tvar koja se stvara u Vašem tijelu i dovodi do sužavanja krvnih
žila, čime se povisuje krvni tlak.
Micardis blokira učinak angiotenzina II, tako da se krvne žile
šire, a krvni tlak snižava.
MICARDIS SE PRIMJENJUJE u liječenju esencijalne hipertenzije (visoki
krvni tlak) u odraslih osoba.
„Esencijalna“ znači da visoki krvni tlak nije izazvan nekom
drugom bolešću.
Visoki krvni tlak, ako se ne liječi, može oštetiti krvne žile u
različitim organima, što ponekad može
dovesti do srčanog udara, zatajenja srca ili bubrega, moždanog udara
ili sljepoće. Prije pojave
oštećenja obično nema simptoma visokog krvnog tlaka. Stoga je
važno redovito mjeriti krvni tlak i
pratiti je li unutar normalnog raspona.
MICARDIS SE TAKOĐER PRIMJENJUJE za smanjivanje kardiovaskularnih
događaja (tj. srčanog udara ili
moždanog udara) u rizičnih odraslih osoba koji imaju smanjenu ili
prekinutu opskrbu krvlju srca ili
nogu, ili su imali moždani udar, ili imaju šećernu bolest s v
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOG I.
SAŽETAK OPISA SVOJSTAVA LIJEKA
2
1.
NAZIV LIJEKA
Micardis 20 mg tablete
Micardis 40 mg tablete
Micardis 80 mg tablete
2.
KVALITATIVNI I KVANTITATIVNI SASTAV
Micardis 20 mg tablete
Jedna tableta sadrži 20 mg telmisartana.
Micardis 40 mg tablete
Jedna tableta sadrži 40 mg telmisartana.
Micardis 80 mg tablete
Jedna tableta sadrži 80 mg telmisartana.
Pomoćne tvari s poznatim učinkom
Jedna tableta od 20 mg sadrži 84 mg sorbitola (E420).
Jedna tableta od 40 mg sadrži 169 mg sorbitola (E420).
Jedna tableta od 80 mg sadrži 338 mg sorbitola (E420).
Za cjeloviti popis pomoćnih tvari vidjeti dio 6.1.
3.
FARMACEUTSKI OBLIK
Tableta
Micardis 20 mg tablete
Bijele, okrugle tablete od 2,5 mm s utisnutom oznakom „50H“ na
jednoj strani i logom tvrtke na
drugoj strani.
Micardis 40 mg tablete
Bijele, duguljaste tablete od 3,8 mm s utisnutom oznakom „51H“ na
jednoj strani i logom tvrtke na
drugoj strani.
Micardis 80 mg tablete
Bijele, duguljaste tablete od 4,6 mm s utisnutom oznakom „52H“ na
jednoj strani i logom tvrtke na
drugoj strani.
4.
KLINIČKI PODACI
4.1
TERAPIJSKE INDIKACIJE
Hipertenzija
Liječenje esencijalne hipertenzije u odraslih osoba.
Kardiovaskularna prevencija
Smanjenje kardiovaskularnog morbiditeta u odraslih osoba s:

manifestnom aterotrombotskom kardiovaskularnom bolešću (anamneza
koronarne bolesti srca,
3
moždanog udara ili periferne arterijske bolesti) ili

šećernom bolešću tipa 2 s dokazanim oštećenjem ciljnih organa
4.2
DOZIRANJE I NAČIN PRIMJENE
Doziranje
_Liječenje esencijalne hipertenzije_
Uobičajena učinkovita doza je 40 mg jedanput na dan. Pojedini
bolesnici mogu imati pozitivan učinak
već pri dnevnoj dozi od 20 mg. U slučajevima gdje nije postignuta
ciljana vrijednost krvnog tlaka,
doza telmisartana može se povisiti na maksimalno 80 mg jedanput na
dan. Kao alternativa, telmisartan
se može primjenjivati u kombinaciji s tiazidnim diureticima, kao što
je hidroklorotiazid, za koji se
pokazalo da ima dodatan učinak na snižavanje krvnog tlaka s
telmisa
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 03-11-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 03-11-2022
Public Assessment Report Public Assessment Report Bulgarian 06-11-2015
Patient Information leaflet Patient Information leaflet Spanish 03-11-2022
Public Assessment Report Public Assessment Report Spanish 06-11-2015
Patient Information leaflet Patient Information leaflet Czech 03-11-2022
Public Assessment Report Public Assessment Report Czech 06-11-2015
Patient Information leaflet Patient Information leaflet Danish 03-11-2022
Public Assessment Report Public Assessment Report Danish 06-11-2015
Patient Information leaflet Patient Information leaflet German 03-11-2022
Public Assessment Report Public Assessment Report German 06-11-2015
Patient Information leaflet Patient Information leaflet Estonian 03-11-2022
Public Assessment Report Public Assessment Report Estonian 06-11-2015
Patient Information leaflet Patient Information leaflet Greek 03-11-2022
Public Assessment Report Public Assessment Report Greek 06-11-2015
Patient Information leaflet Patient Information leaflet English 03-11-2022
Public Assessment Report Public Assessment Report English 06-11-2015
Patient Information leaflet Patient Information leaflet French 03-11-2022
Public Assessment Report Public Assessment Report French 06-11-2015
Patient Information leaflet Patient Information leaflet Italian 03-11-2022
Public Assessment Report Public Assessment Report Italian 06-11-2015
Patient Information leaflet Patient Information leaflet Latvian 03-11-2022
Public Assessment Report Public Assessment Report Latvian 06-11-2015
Patient Information leaflet Patient Information leaflet Lithuanian 03-11-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 03-11-2022
Public Assessment Report Public Assessment Report Lithuanian 06-11-2015
Patient Information leaflet Patient Information leaflet Hungarian 03-11-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 03-11-2022
Public Assessment Report Public Assessment Report Hungarian 06-11-2015
Patient Information leaflet Patient Information leaflet Maltese 03-11-2022
Public Assessment Report Public Assessment Report Maltese 06-11-2015
Patient Information leaflet Patient Information leaflet Dutch 03-11-2022
Public Assessment Report Public Assessment Report Dutch 06-11-2015
Patient Information leaflet Patient Information leaflet Polish 03-11-2022
Public Assessment Report Public Assessment Report Polish 06-11-2015
Patient Information leaflet Patient Information leaflet Portuguese 03-11-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 03-11-2022
Public Assessment Report Public Assessment Report Portuguese 06-11-2015
Patient Information leaflet Patient Information leaflet Romanian 03-11-2022
Public Assessment Report Public Assessment Report Romanian 06-11-2015
Patient Information leaflet Patient Information leaflet Slovak 03-11-2022
Public Assessment Report Public Assessment Report Slovak 06-11-2015
Patient Information leaflet Patient Information leaflet Slovenian 03-11-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 03-11-2022
Public Assessment Report Public Assessment Report Slovenian 06-11-2015
Patient Information leaflet Patient Information leaflet Finnish 03-11-2022
Public Assessment Report Public Assessment Report Finnish 06-11-2015
Patient Information leaflet Patient Information leaflet Swedish 03-11-2022
Public Assessment Report Public Assessment Report Swedish 06-11-2015
Patient Information leaflet Patient Information leaflet Norwegian 03-11-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 03-11-2022
Patient Information leaflet Patient Information leaflet Icelandic 03-11-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 03-11-2022

Search alerts related to this product

View documents history