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

vyvgart

argenx - efgartigimod alfa - myasthenia gravis - immunsuppressiva - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.

Teriflunomide Mylan Europeiska unionen - svenska - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - multipel skleros, skovvis förlöpande - immunsuppressiva - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Teriflunomide Newbury 14 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

teriflunomide newbury 14 mg filmdragerad tablett

newbury pharmaceuticals ab - teriflunomid - filmdragerad tablett - 14 mg - laktosmonohydrat hjälpämne; teriflunomid 14 mg aktiv substans

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

spevigo

boehringer ingelheim international gmbh - spesolimab - psoriasis - immunsuppressiva - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

Dimethyl fumarate Newbury 240 mg Enterokapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

dimethyl fumarate newbury 240 mg enterokapsel, hård

newbury pharmaceuticals ab - dimetylfumarat - enterokapsel, hård - 240 mg - dimetylfumarat 240 mg aktiv substans; propylenglykol hjälpämne

Dimethyl fumarate Newbury 120 mg Enterokapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

dimethyl fumarate newbury 120 mg enterokapsel, hård

newbury pharmaceuticals ab - dimetylfumarat - enterokapsel, hård - 120 mg - dimetylfumarat 120 mg aktiv substans; propylenglykol hjälpämne

Lacosamide Adroiq Europeiska unionen - svenska - EMA (European Medicines Agency)

lacosamide adroiq

extrovis eu ltd. - lakosamid - epilepsi - antiepileptika, - lacosamide adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. lacosamide adroiq is indicated as adjunctive therapyin the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Lacosamide Medical Valley 150 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

lacosamide medical valley 150 mg filmdragerad tablett

medical valley invest ab - lakosamid - filmdragerad tablett - 150 mg - lakosamid 150 mg aktiv substans

Lacosamide Medical Valley 200 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

lacosamide medical valley 200 mg filmdragerad tablett

medical valley invest ab - lakosamid - filmdragerad tablett - 200 mg - lakosamid 200 mg aktiv substans

Lacosamide Medical Valley 100 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

lacosamide medical valley 100 mg filmdragerad tablett

medical valley invest ab - lakosamid - filmdragerad tablett - 100 mg - lakosamid 100 mg aktiv substans