Aimovig Европска Унија - Шведски - EMA (European Medicines Agency)

aimovig

novartis europharm limited - erenumab - migrän störningar - smärtstillande medel - aimovig är indicerat för profylax av migrän hos vuxna som har minst 4 migrän dagar per månad vid insättande av behandling med aimovig.

Beovu Европска Унија - Шведски - EMA (European Medicines Agency)

beovu

novartis europharm limited  - brolucizumab - wet macular degeneration - ögonsjukdomar - beovu är indicerat hos vuxna för behandling av neovaskulära (våt) åldersrelaterad makuladegeneration (amd).

Zolgensma Европска Унија - Шведски - EMA (European Medicines Agency)

zolgensma

novartis europharm limited  - onasemnogene abeparvovec - muskelatrofi, ryggrad - andra droger för sjukdomar i muskel-skelettsystemet - zolgensma är indicerat för behandling av: - patienter med 5q spinal muskelatrofi (sma) med en bi-genetisk mutation i smn1-genen och en klinisk diagnos av sma typ 1, orpatients med 5q sma med en bi-genetisk mutation i smn1-genen och upp till 3 kopior av den gen smn2.

Enerzair Breezhaler Европска Унија - Шведски - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - läkemedel mot obstruktiv lungsjukdom, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Bemrist Breezhaler Европска Унија - Шведски - EMA (European Medicines Agency)

bemrist breezhaler

novartis europharm limited  - indacaterol, mometasone furoate - astma - läkemedel mot obstruktiv lungsjukdom, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Zimbus Breezhaler Европска Унија - Шведски - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - läkemedel mot obstruktiv lungsjukdom, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Adakveo Европска Унија - Шведски - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemi, sickle cell - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Leqvio Европска Унија - Шведски - EMA (European Medicines Agency)

leqvio

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - lipidmodifierande medel - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin, oralone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

Kesimpta Европска Унија - Шведски - EMA (European Medicines Agency)

kesimpta

novartis ireland ltd - ofatumumab - multipel skleros, skovvis förlöpande - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Tabrecta Европска Унија - Шведски - EMA (European Medicines Agency)

tabrecta

novartis europharm limited  - capmatinib dihydrochloride monohydrate - carcinom, non-small cell lung - antineoplastiska medel - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.