Tegsedi Den europeiske union - islandsk - EMA (European Medicines Agency)

tegsedi

akcea therapeutics ireland limited - inotersen járn - amyloidosis - Önnur lyf í taugakerfinu - meðferð stigi 1 eða stigi 2 polyneuropathy í fullorðinn sjúklinga með arfgenga transthyretin amyloidosis (hattr).

Ganirelix Gedeon Richter Den europeiske union - islandsk - EMA (European Medicines Agency)

ganirelix gedeon richter

chemical works of gedeon richter plc. (gedeon richter plc.) - ganirelix acetate - reproductive techniques, assisted; ovulation induction; infertility, female - hinsveiflur og heilahimnubólur og hliðstæður - prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation (coh) for assisted reproduction techniques (art).

Ovitrelle Den europeiske union - islandsk - EMA (European Medicines Agency)

ovitrelle

merck europe b.v. - choriogonadotropin alfa - anovulation; reproductive techniques, assisted; infertility, female - hormón kynlíf og stillum kynfæri - ovitrelle er ætlað í meðferð:konur gangast undir myndun fjölda eggja samtímis fyrir að aðstoða æxlun aðferðir eins og glasafrjóvgun (tÆknifrjÓvgun): ovitrelle er gefið til að kveikja endanleg tíðahvörf þroska og luteinisation eftir örvun tíðahvörf vöxt;haft egglos eða oligo-egglos konur: ovitrelle er gefið til að kveikja egglos og luteinisation í haft egglos eða oligo-egglos sjúklinga eftir örvun tíðahvörf vöxt.

Dupixent Den europeiske union - islandsk - 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.

Elonva Den europeiske union - islandsk - EMA (European Medicines Agency)

elonva

n.v. organon - corifollitropin alfa - reproductive techniques, assisted; ovulation induction; investigative techniques - hormón kynlíf og stillum kynfæri - controlled ovarian stimulation (cos) in combination with a gnrh antagonist for the development of multiple follicles in women participating in an assisted reproductive technology (art) program. elonva is indicated for the treatment of adolescent males (14 to less than 18 years and older) with hypogonadotropic hypogonadism, in combination with human chorionic gonadotropin (hcg).

Firazyr Den europeiske union - islandsk - EMA (European Medicines Agency)

firazyr

takeda pharmaceuticals international ag - icatibant - ofsabjúgur, arfgengur - hjarta meðferð - firazyr er ætlað til meðferðar við bráðri árás arfgengs ofsabjúgs (hae) hjá fullorðnum (með skort á c1-esterasa-hemlum).

Icatibant Accord Den europeiske union - islandsk - EMA (European Medicines Agency)

icatibant accord

accord healthcare s.l.u. - icatibant acetate - ofsabjúgur, arfgengur - other hematological agents - icatibant accord is indicated for symptomatic treatment of acute attacks of hereditary angioedema (hae) in adults, adolescents and children aged 2 years and older, with c1 esterase inhibitor deficiency.

Amvuttra Den europeiske union - islandsk - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - Önnur lyf í taugakerfinu - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Buvidal Den europeiske union - islandsk - EMA (European Medicines Agency)

buvidal

camurus ab - búprenorfín - Ópíóíð-tengdir sjúkdómar - Önnur lyf í taugakerfinu - meðferð um lifur fíkn innan ramma læknis, félagslegar og sálfræðileg meðferð. meðferð er ætlað til að nota í fullorðnir og unglingar á aldrinum 16 ár eða yfir.

Fulvestrant Mylan Den europeiske union - islandsk - EMA (European Medicines Agency)

fulvestrant mylan

mylan pharmaceuticals limited - fulvestrant - brjóstakrabbamein - innkirtla meðferð - fulvestrant er ætlað fyrir meðferð estrógen viðtaka jákvætt, á staðnum háþróaður eða brjóstakrabbamein í tíðahvörf konur:ekki áður meðhöndluð með annarra meðferð, eðameð sjúkdómur bakslag eða á eftir viðbótar anti-estrógen meðferð, eða sjúkdóms á andestrógeni meðferð.