الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

novartis europharm limited - dabrafenib mesilate - melanoma - antineoplastična sredstva - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 in 5. adjuvant zdravljenje melanomadabrafenib v kombinaciji z trametinib je primerna za adjuvant zdravljenje odraslih bolnikov z faza iii melanoma z braf v600 mutacije, po popolna resekcija. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

accord healthcare s.l.u. - dabigatran etexilate mesilate - venous thromboembolism; arthroplasty, replacement - antitrombotična sredstva - prevention of venous thromboembolic events.

سلوفينيا - السلوفانية - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kemofarmacija d.d. - dihidralazinijev mesilat - prašek in vehikel za raztopino za injiciranje - dihidralazinijev mesilat 12,5 mg / 1 ml - dihidralazin

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

eisai gmbh - lenvatinib mesilat - karcinom, ledvična celica - antineoplastična sredstva - kisplyx is indicated for the treatment of adults with advanced renal cell carcinoma (rcc):in combination with pembrolizumab, as first-line treatment (see section 5. in combination with everolimus, following one prior vascular endothelial growth factor (vegf)-targeted therapy.

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

eisai gmbh - lenvatinib mesilat - Širokopasemske neoplazme - antineoplastična sredstva - lenvima je označen kot monotherapy za zdravljenje odraslih bolnikov z napredujočo, lokalno napredno ali metastatskim, diferencirana (papillary/folikularni/hürthle celic) karcinom ščitnice (dtc), ognjevzdržni, da se radioaktivni jod (rai). lenvima je označen kot monotherapy za zdravljenje odraslih bolnikov z napredovalim ali unresectable hepatocellular carcinoma (hcc), ki so prejeli brez predhodnega sistemske terapije.

سلوفينيا - السلوفانية - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

lenis d.o.o. - atrakurijev besilat - raztopina za injiciranje - atrakurijev besilat 50 mg / 5 ml - atrakurium

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

viatris limited - klopidogrel besilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotična sredstva - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. adult patients suffering from acute coronary syndrome. non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). st segmentu višinskih akutni miokardni infarkt, v kombinaciji s asa v medicinsko zdravljenih bolnikih, ki izpolnjujejo pogoje za thrombolytic terapija. in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is) clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2 score ≥4) or minor is (nihss ≤3) within 24 hours of either the tia or is event. prevention of atherothrombotic and thromboembolic events in atrial fibrillation:in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. za nadaljnje informacije, prosimo, preberite razdelek 5.

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

mylan pharmaceuticals limited - amlodipine besilate, valsartan - hipertenzija - sredstva, ki delujejo na sistem renin-angiotenzin - zdravljenje esencialne hipertenzije. amlodipine/valsartan mylan je navedeno pri odraslih, katerih krvni tlak ni ustrezno nadzorovan na amlodipine ali valsartan monotherapy.

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - hipertenzija - sredstva, ki delujejo na sistem renin-angiotenzin - zdravljenje esencialne hipertenzije. copalia je indicirana pri bolnikih, katerih krvni tlak ni ustrezno nadzorovan na amlodipine ali valsartan monotherapy.

الاتحاد الأوروبي - السلوفانية - EMA (European Medicines Agency)

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - hipertenzija - sredstva, ki delujejo na sistem renin-angiotenzin - zdravljenje esencialne hipertenzije. exforge je indicirana pri bolnikih, katerih krvni tlak ni ustrezno nadzorovan na amlodipine ali valsartan monotherapy.