Esomeprazol AstraZeneca 40 mg gastrorezistentne tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

esomeprazol astrazeneca 40 mg gastrorezistentne tablete

astrazeneca uk limited - esomeprazol - gastrorezistentna tableta - esomeprazol 40 mg / 1 tableta - esomeprazol

Esomeprazol AstraZeneca 20 mg gastrorezistentne tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

esomeprazol astrazeneca 20 mg gastrorezistentne tablete

astrazeneca uk limited - esomeprazol - gastrorezistentna tableta - esomeprazol 20 mg / 1 tableta - esomeprazol

Nexium 20 mg gastrorezistentne tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

nexium 20 mg gastrorezistentne tablete

astrazeneca uk limited - esomeprazol - gastrorezistentna tableta - esomeprazol 20 mg / 1 tableta - esomeprazol

Anoro Ellipta (previously Anoro) Evropska unija - slovenščina - EMA (European Medicines Agency)

anoro ellipta (previously anoro)

glaxosmithkline (ireland) limited - umeclidinium bromid, vilanterol trifenatate - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - anoro ellipta je označen kot vzdrževanje bronchodilator zdravljenje za lajšanje simptomov pri odraslih bolnikih s kronično obstruktivno pljučno bolezen (kopb).

Benlysta Evropska unija - slovenščina - EMA (European Medicines Agency)

benlysta

glaxosmithkline (ireland) limited - belimumab - lupus erythematosus, sistemski - imunosupresivi - benlysta je indicirano kot dodatek terapije pri bolnikih, starih 5 let in več, z aktivno, autoantibody pozitivno sistemski eritematozni lupus (sle), z visoko stopnjo aktivnosti bolezni (e. pozitivni anti dsdna in nizko dopolnitev) kljub standardne terapije. benlysta is indicated in combination with background immunosuppressive therapies for the treatment of adult patients with active lupus nephritis.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Evropska unija - slovenščina - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

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.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Evropska unija - slovenščina - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - klopidogrel hidroklorid - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - 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), ischaemic 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 segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , 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. , , for further information please refer to section 5. , , ,.

Incruse Ellipta (previously Incruse) Evropska unija - slovenščina - EMA (European Medicines Agency)

incruse ellipta (previously incruse)

glaxosmithkline (ireland) limited - umeclidinium bromid - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - označena kot zdravljenje bronhodilatatorjev za vzdrževanje simptomov pri odraslih bolnikih s kronično obstruktivno pljučno boleznijo (kopb).

Laventair Ellipta (previously Laventair) Evropska unija - slovenščina - EMA (European Medicines Agency)

laventair ellipta (previously laventair)

glaxosmithkline (ireland) limited - umeclidinium bromid, vilanterol - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - laventair ellipta je označen kot vzdrževanje bronchodilator zdravljenje za lajšanje simptomov pri odraslih bolnikih s kronično obstruktivno pljučno bolezen (kopb).

Rolufta Ellipta (previously Rolufta) Evropska unija - slovenščina - EMA (European Medicines Agency)

rolufta ellipta (previously rolufta)

glaxosmithkline trading services limited - umeclidinium bromid - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - zdravilo rolufta je indicirano za zdravljenje bronhodilatatorjev za vzdrževanje simptomov pri odraslih bolnikih s kronično obstruktivno pljučno boleznijo (kopb).