Possia האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

possia

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitrombotična sredstva - possia, co-upravlja z acetilsalicilna kislina (asa), je indiciran za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih z akutni koronarni sindrom (nestabilna angina pektoris, non-st-infarkta miokarda [nstemi] ali st-nadmorske višine miokardni infarkt [stemi]); vključno z bolniki, ki upravlja z zdravili, in tistih, ki so z perkutano koronarno intervencijo (pci) ali koronarne arterije cepljenje obvod (cabg).

Tagrisso האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

tagrisso

astrazeneca ab - osimertinib mesilate - karcinom, pljučni pljuč - druga zdravila z delovanjem na novotvorbe agenti, protein kinaza inhibitorji - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Lynparza האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

lynparza

astrazeneca ab - olaparib - ovarijske neoplazme - antineoplastična sredstva - ciste na cancerlynparza je označen kot monotherapy za:vzdrževanje zdravljenje odraslih bolnikov z napredovalim (figo fazah iii in iv) brca1/2-mutiral (germline in/ali somatski) high-grade epitelnih jajčnikov, fallopian tube ali primarni trebušno raka, ki so v odziv (popolna ali delna) po koncu prve vrstice platinum, ki temelji kemoterapijo. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5. breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4. 2 in 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. bolniki morajo imeti predhodno že bili zdravljeni z anthracycline in taxane v (neo)adjuvant ali metastatskim nastavitev, če bolniki niso bili primerni za temi postopki (glej točko 5. bolniki z hormon receptorjev (hr)-pozitivnega raka dojk, je treba tudi napredovala na ali po predhodnem endokrine terapije, ali neprimerna za endokrine terapija. adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.

Daliresp האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

daliresp

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - daliresp je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek bronchodilator zdravljenje.

Libertek האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

libertek

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - libertek je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek bronchodilator zdravljenje.

Ovixan 1 mg/g dermalna raztopina סלובניה - סלובנית - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

ovixan 1 mg/g dermalna raztopina

galenica ab - mometazonfuroat - dermalna raztopina - mometazonfuroat 1 mg / 1 g - mometazon

Brilique האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

brilique

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitrombotična sredstva - brilique, co daje z acetilsalicilne kisline (asa), je označen za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih withacute koronarnih sindromov (acs), zdaj zgodovino miokardni infarkt (mi) in visokim tveganjem za razvoj atherothrombotic eventbrilique, co-daje z acetil salicilna kislina (asa), je označen za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih z anamnezo miokardni infarkt (mi je prišlo, najmanj eno leto nazaj) in visokim tveganjem za razvoj atherothrombotic dogodek.

Daxas האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

daxas

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - daxas je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek za bronchodilator zdravljenje.

Ebymect האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

ebymect

astrazeneca ab - dapagliflozin propanediol monohidrat, metformin hidroklorid - diabetes mellitus, tip 2 - zdravila, ki se uporabljajo pri diabetesu - diabetes tipa 2 mellitusfor zdravljenje ni dovolj nadzorovano tipa 2 sladkorna bolezen kot dodatek k dieti in telesni. kot monotherapy ko metformin je neprimerno zaradi nestrpnosti. poleg drugimi zdravili za zdravljenje diabetesa tipa 2. za študijski rezultati glede kombinacija terapij, vplivi na glycaemic nadzor in srčno-žilne dogodke, in populacije, ki je študiral glej poglavji 4. 4, 4. 5 in 5. sladkorna bolezen tipa 1 mellitusedistride je navedeno pri odraslih za zdravljenje premalo nadzorovana sladkorna bolezen tipa 1 kot dodatek k insulina pri bolnikih z itm ≥ 27 kg/m2, če insulin sam ne zagotavljajo ustrezne glycaemic nadzor kljub optimalno insulina terapija.

Edistride האיחוד האירופי - סלובנית - EMA (European Medicines Agency)

edistride

astrazeneca ab - dapagliflozin propandiol monohidrat - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - zdravila, ki se uporabljajo pri diabetesu - type 2 diabetes mellitusedistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. poleg drugimi zdravili za zdravljenje diabetesa tipa 2. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 in 5. heart failureedistride is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseedistride is indicated in adults for the treatment of chronic kidney disease.