Vionate 35 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

vionate 35 mg filmdragerad tablett

mylan ab - risedronatnatrium-2,5-hydrat - filmdragerad tablett - 35 mg - risedronatnatrium-2,5-hydrat 40,17 mg aktiv substans; laktosmonohydrat hjälpämne - risedronsyra

Vionate 5 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

vionate 5 mg filmdragerad tablett

mylan ab - risedronatnatrium-2,5-hydrat - filmdragerad tablett - 5 mg - laktosmonohydrat hjälpämne; risedronatnatrium-2,5-hydrat 5,74 mg aktiv substans - risedronsyra

Dapagliflozin Viatris Europeiska unionen - svenska - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - läkemedel som används vid 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 och 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.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Europeiska unionen - svenska - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - klopidogrelbesilat - peripheral vascular diseases; stroke; myocardial infarction - antitrombotiska medel - 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-segmentet höjd akut hjärtinfarkt, i kombination med asa i medicinskt behandlade patienter berättigade till trombolysbehandling. 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. för ytterligare information hänvisas till avsnitt 5.

Pirfenidone Viatris Europeiska unionen - svenska - EMA (European Medicines Agency)

pirfenidone viatris

viatris limited - pirfenidon - idiopathic pulmonary fibrosis; lung diseases; respiratory tract diseases - immunsuppressiva - pirfenidone viatris is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Imatinib Viatris 400 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

imatinib viatris 400 mg filmdragerad tablett

viatris limited - imatinibmesilat - filmdragerad tablett - 400 mg - imatinibmesilat 478 mg aktiv substans

Incivo Europeiska unionen - svenska - EMA (European Medicines Agency)

incivo

janssen-cilag international n.v. - telaprevir - hepatit c, kronisk - antivirala medel för systemisk användning - incivo, i kombination med peginterferon alfa och ribavirin, är indicerat för behandling av genotyp-1 kronisk hepatit c hos vuxna patienter med kompenserad leversjukdom (inklusive cirros):vem är behandling naiva, de som tidigare behandlats med interferon alfa (pegylerat eller icke-pegylerat) ensamt eller i kombination med ribavirin, inklusive relapsers, partiella responders null responders.

Apixaban Viatris 5 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

apixaban viatris 5 mg filmdragerad tablett

viatris limited - apixaban - filmdragerad tablett - 5 mg - laktosmonohydrat hjälpämne; natriumlaurilsulfat hjälpämne; apixaban 5 mg aktiv substans; laktos (vattenfri) hjälpämne

Apixaban Viatris 2,5 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

apixaban viatris 2,5 mg filmdragerad tablett

viatris limited - apixaban - filmdragerad tablett - 2,5 mg - natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne; laktos (vattenfri) hjälpämne; apixaban 2,5 mg aktiv substans

Pantoprazol Viatris 40 mg Enterotablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pantoprazol viatris 40 mg enterotablett

viatris limited - pantoprazolnatriumseskvihydrat - enterotablett - 40 mg - pantoprazolnatriumseskvihydrat 45,1 mg aktiv substans; mannitol hjälpämne; natriumlaurilsulfat hjälpämne - pantoprazol