Zontivity Den europeiske union - norsk - EMA (European Medicines Agency)

zontivity

merck sharp dohme limited - vorapaxar sulfat - hjerteinfarkt - antithrombotic agents - zontivityis indikert for reduksjon av atherothrombotic hendelser hos voksne pasienter med en historie med hjerteinfarkt (mi)co-gis med acetylsalisylsyre (asa) og, der det er hensiktsmessig, klopidogrel, eller - symptomatisk perifere arterial sykdom(pad), co-gis med acetylsalisylsyre (asa) eller, der det er hensiktsmessig, clopidogrel.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Den europeiske union - norsk - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - klopidogrel besilat - peripheral vascular diseases; stroke; myocardial infarction - 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), 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-segment elevasjon akutte myocardial infarction, i kombinasjon med asa i medisinsk behandlede pasienter kvalifisert for trombolytisk behandling. 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 ytterligere informasjon, vennligst referer til seksjon 5.

Abiraterone Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

abiraterone mylan

mylan ireland limited - abirateronacetat - prostata neoplasmer - endocrine therapy, other hormone antagonists and related agents - abiraterone mylan is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt). the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated. the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Atenolol Viatris 50 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 50 mg

viatris limited - atenolol - tablett, filmdrasjert - 50 mg

Atenolol Viatris 25 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 25 mg

viatris limited - atenolol - tablett, filmdrasjert - 25 mg

Atenolol Viatris 100 mg Norge - norsk - Statens legemiddelverk

atenolol viatris 100 mg

viatris limited - atenolol - tablett, filmdrasjert - 100 mg

Sotalol Viatris 40 mg Norge - norsk - Statens legemiddelverk

sotalol viatris 40 mg

viatris limited - sotalolhydroklorid - tablett - 40 mg

Sotalol Viatris 80 mg Norge - norsk - Statens legemiddelverk

sotalol viatris 80 mg

viatris limited - sotalolhydroklorid - tablett - 80 mg

Opgenra Den europeiske union - norsk - EMA (European Medicines Agency)

opgenra

olympus biotech international limited - eptotermin alfa - spondylolisthesis - legemidler til behandling av bein sykdommer - opgenra er indisert for posterolateral lumbal spinal fusion hos voksne pasienter med spondylolistese hvor autograft har mislyktes eller er kontraindisert.

Dapagliflozin Viatris Den europeiske union - norsk - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - legemidler som brukes i diabetes - type 2 diabetes mellitusdapagliflozin viatris 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 exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. 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 og 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.