Dupixent Liên Minh Châu Âu - Tiếng Iceland - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - umboðsmenn fyrir húðbólgu, að undanskildu barkstera - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Rasilamlo Liên Minh Châu Âu - Tiếng Iceland - EMA (European Medicines Agency)

rasilamlo

novartis europharm ltd - aliskiren, meðferð - háþrýstingur - lyf sem hafa áhrif á renín-angíótensín kerfið - rasilamlo er ætlað til meðhöndlunar á nauðsynlegum háþrýstingi hjá fullorðnum sjúklingum, þar sem blóðþrýstingur er ekki nægilega stjórnað með aliskireni eða amlodipini sem er notað eitt sér.

Elvanse Adult Hart hylki 30 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 30 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 30 mg

Elvanse Adult Hart hylki 50 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 50 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 50 mg

Elvanse Adult Hart hylki 70 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 70 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 70 mg

Elvanse Adult Hart hylki 20 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 20 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 20 mg

Elvanse Adult Hart hylki 40 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 40 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 40 mg

Elvanse Adult Hart hylki 60 mg Iceland - Tiếng Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

elvanse adult hart hylki 60 mg

takeda pharmaceuticals international ag ireland branch - lisdexamfetaminum dimesylate - hart hylki - 60 mg

Mycapssa Liên Minh Châu Âu - Tiếng Iceland - EMA (European Medicines Agency)

mycapssa

amryt pharmaceuticals dac - octreotide acetate - acromegaly - hinsveiflur og heilahimnubólur og hliðstæður - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

Neptra Liên Minh Châu Âu - Tiếng Iceland - EMA (European Medicines Agency)

neptra

bayer animal health gmbh - florfenicol, terbinafin stutt og long-term, mometasone furoate - otologicals, krefur og antiinfectives í samsetning - hundar - fyrir meðferð bráð hundur bólgu í ytra eða bráð tilvikum endurtekin eyrnabólga af völdum blandað sýkingar næm stofnum bakteríur viðkvæm florfenicol (Þegar pseudintermedius) og sveppi viðkvæm terbinafin (malassezia pachydermatis).