Aduvanz 30 mg นอร์เวย์ - นอร์เวย์ - Statens legemiddelverk

aduvanz 30 mg

takeda pharmaceuticals international ag ireland branch - lisdeksamfetamindimesilat - kapsel, hard - 30 mg

Aduvanz 70 mg นอร์เวย์ - นอร์เวย์ - Statens legemiddelverk

aduvanz 70 mg

takeda pharmaceuticals international ag ireland branch - lisdeksamfetamindimesilat - kapsel, hard - 70 mg

Qinlock สหภาพยุโรป - นอร์เวย์ - EMA (European Medicines Agency)

qinlock

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - gastrointestinal stromal tumors - antineoplastiske midler - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

Aduvanz 20 mg นอร์เวย์ - นอร์เวย์ - Statens legemiddelverk

aduvanz 20 mg

takeda pharmaceuticals international ag ireland branch - lisdeksamfetamindimesilat - kapsel, hard - 20 mg

Aduvanz 40 mg นอร์เวย์ - นอร์เวย์ - Statens legemiddelverk

aduvanz 40 mg

takeda pharmaceuticals international ag ireland branch - lisdeksamfetamindimesilat - kapsel, hard - 40 mg

Aduvanz 60 mg นอร์เวย์ - นอร์เวย์ - Statens legemiddelverk

aduvanz 60 mg

takeda pharmaceuticals international ag ireland branch - lisdeksamfetamindimesilat - kapsel, hard - 60 mg

Clopidogrel ratiopharm สหภาพยุโรป - นอร์เวย์ - EMA (European Medicines Agency)

clopidogrel ratiopharm

teva b.v. - clopidogrel (as hydrogen sulfate) - myocardial infarction; acute coronary syndrome; peripheral vascular diseases; stroke - antithrombotic agents - 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. voksne pasienter som lider av akutt koronar syndrom:ikke-st-segment elevasjon akutt koronar syndrom (ustabil angina eller non-q-bølge myocardial infarction), inkludert pasienter som gjennomgår en stent plassering etter perkutan koronar intervensjon, i kombinasjon med acetylsalisylsyre (asa). st-segment elevasjon akutte myocardial infarction, i kombinasjon med asa i medisinsk behandlede pasienter kvalifisert for trombolytisk behandling. forebygging av atherothrombotic og tromboemboliske hendelser i atrial fibrillationin voksne pasienter med atrieflimmer som har minst en risikofaktor for vaskulære hendelser, er ikke egnet for behandling med vitamin k-antagonister (vka) og som har en lav risiko for blødning, clopidogrel er indisert i kombinasjon med asa for forebygging av atherothrombotic og tromboemboliske hendelser, inkludert hjerneslag.

Raplixa สหภาพยุโรป - นอร์เวย์ - EMA (European Medicines Agency)

raplixa

mallinckrodt pharmaceuticals ireland limited - human fibrinogen, human trombin - hemostase, kirurgisk - antihemoragika - støttende behandling der standard kirurgiske teknikker er utilstrekkelige for forbedring av hemostase. raplixa må brukes i kombinasjon med en godkjent gelatin svamp. raplixa er indisert hos voksne over 18 år.