Brineura Evrópusambandið - íslenska - EMA (European Medicines Agency)

brineura

biomarin international limited - cerliponase alfa - neuronal ceroid-lipofuscinoses - Önnur meltingarvegi og efnaskipti vörur, - brineura er ætlað fyrir meðferð af taugafrumum ceroid lipofuscinosis tegund 2 (cln2) sjúkdómur, einnig þekktur sem tripeptidyl peptidase 1 (tpp1) skort,.

Fontex Dreifitafla 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fontex dreifitafla 20 mg

eli lilly danmark a/s - fluoxetinum hýdróklóríð - dreifitafla - 20 mg

Sabrilex Filmuhúðuð tafla 500 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sabrilex filmuhúðuð tafla 500 mg

sanofi-aventis norge as - vigabatrinum inn - filmuhúðuð tafla - 500 mg

Ionsys Evrópusambandið - íslenska - EMA (European Medicines Agency)

ionsys

incline therapeutics europe ltd - fentanýlhýdróklóríð - verkir, eftir aðgerð - verkjalyf - ionsys er ætlað til meðferðar við bráðum, miðlungsmiklum eða alvarlegum verkjum eftir fullorðna hjá fullorðnum sjúklingum.

Nordimet Evrópusambandið - íslenska - EMA (European Medicines Agency)

nordimet

nordic group b.v. - stendur - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - Æxlishemjandi lyf - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.

Triumeq Evrópusambandið - íslenska - EMA (European Medicines Agency)

triumeq

viiv healthcare b.v. - dolutegravir sodium, lamivudine, abacavir (as sulfate) - hiv sýkingar - veirueyðandi lyf til almennrar notkunar - triumeq is indicated for the treatment of human immunodeficiency virus (hiv) infected adults,  adolescents and children  weighing at least 25 kg who are antiretroviral treatment-naïve or are infected with hiv without documented or clinically suspected resistance to any of the three antiretroviral agents in triumeq.

Vidaza Evrópusambandið - íslenska - EMA (European Medicines Agency)

vidaza

bristol-myers squibb pharma eeig - azasitidín - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - Æxlishemjandi lyf - vidaza is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with: intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification. vidaza is indicated for the treatment of adult patients aged 65 years or older who are not eligible for hsct with aml with >30% marrow blasts according to the who classification.

Fotivda Evrópusambandið - íslenska - EMA (European Medicines Agency)

fotivda

recordati netherlands b.v. - tivozanib - krabbamein, nýrnafrumur - Æxlishemjandi lyf - fotivda er ætlað fyrir fyrstu línuna meðferð fullorðinn sjúklinga með langt skert klefi krabbamein (rcc) og fyrir fullorðna sjúklinga sem eru vegfr og hana ferli hemil-barnalegt eftir sjúkdóms eftir einn meðferð áður með frumuboða meðferð fyrir háþróaður rcc. meðferð háþróaður skert klefi krabbamein.

Imcivree Evrópusambandið - íslenska - EMA (European Medicines Agency)

imcivree

rhythm pharmaceuticals netherlands b.v. - setmelanotide - offita - Ónæmiskerfi, þó ekki mataræði - imcivree is indicated for the treatment of obesity and the control of hunger associated with genetically confirmed bardet biedl syndrome (bbs), loss-of-function biallelic pro-opiomelanocortin (pomc), including pcsk1, deficiency or biallelic leptin receptor (lepr) deficiency in adults and children 6 years of age and above.

Yselty Evrópusambandið - íslenska - EMA (European Medicines Agency)

yselty

theramex ireland limited - linzagolix choline - leiomyoma - hinsveiflur og heilahimnubólur og hliðstæður - yselty is indicated for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.