Cernevit Stungulyfsstofn, lausn Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cernevit stungulyfsstofn, lausn

baxter medical ab* - vítamín a (palmítat); colecalciferolum inn; vítamín e (tocoferolum nfn); acidum ascorbicum inn; thiaminum cocarboxylase tetrahýdrat; riboflavinum natríumfosfat díhýdrat; pyridoxinum hýdróklóríð; cyanocobalaminum inn; acidum folicum inn; dexpanthenolum inn; biotinum inn; nicotinamidum inn - stungulyfsstofn, lausn

Vitamin AD3E pro injectione Stungulyf, lausn 176,47 / 50 / 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vitamin ad3e pro injectione stungulyf, lausn 176,47 / 50 / 100 mg/ml

bela-pharm gmbh & co. kg - retinol palmitate; colecalciferolum inn; all-rac-alpha-tocopheryl acetate - stungulyf, lausn - 176,47 / 50 / 100 mg/ml

Vitalipid Adult Innrennslisþykkni, fleyti Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vitalipid adult innrennslisþykkni, fleyti

fresenius kabi ab - vítamín a (palmítat); phytomenadionum inn; ergocalciferolum inn; vítamín e (tocoferolum nfn) - innrennslisþykkni, fleyti

Vitalipid Infant Innrennslisþykkni, fleyti Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vitalipid infant innrennslisþykkni, fleyti

fresenius kabi ab - vítamín a (palmítat); vítamín e (tocoferolum nfn); phytomenadionum inn; ergocalciferolum inn - innrennslisþykkni, fleyti

Vedrop Evrópusambandið - íslenska - EMA (European Medicines Agency)

vedrop

recordati rare diseases - tocofersolan - cholestasis; vitamin e deficiency - vítamín - vedrop er ætlað í d-e skort vegna meltingu vanfrásog í börn sjúklingar sem þjáist af meðfæddri langvarandi gallteppu eða arfgenga langvarandi gallteppu, frá fæðingu (í tíma börn) til 16 eða 18 ára aldri, eftir á svæðinu.

Eucreas Evrópusambandið - íslenska - EMA (European Medicines Agency)

eucreas

novartis europharm limited - vildagliptin, kvarta stutt og long-term - sykursýki, tegund 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Evrópusambandið - íslenska - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, kvarta stutt og long-term - sykursýki, tegund 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 og 5. 1 fyrir tiltæk gögn um mismunandi samsetningar).

Vipdomet Evrópusambandið - íslenska - EMA (European Medicines Agency)

vipdomet

takeda pharma a/s - rannsóknir á dýra, kvarta stutt og long-term - sykursýki, tegund 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. þrefaldur samsetning meðferð) sem viðbót til að fæði og æfa til að bæta blóðsykursstjórnun í sjúklinga þegar insúlín í stöðugu skammtur og kvarta einn veita ekki fullnægjandi blóðsykursstjórnun.

Segluromet Evrópusambandið - íslenska - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - sykursýki, tegund 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Venclyxto Evrópusambandið - íslenska - EMA (European Medicines Agency)

venclyxto

abbvie deutschland gmbh co. kg - venetoclax - kyrningahvítblæði, eitilfrumnafæð, langvarandi, b-frumur - Æxlishemjandi lyf - venclyxto in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. venclyxto in combination with rituximab is indicated for the treatment of adult patients with cll who have received at least one prior therapy. venclyxto monotherapy is indicated for the treatment of cll:- in the presence of 17p deletion or tp53 mutation in adult patients who are unsuitable for or have failed a b cell receptor pathway inhibitor, or- in the absence of 17p deletion or tp53 mutation in adult patients who have failed both chemoimmunotherapy and a b-cell receptor pathway inhibitor. venclyxto in combination with a hypomethylating agent is indicated for the treatment of adult patients with newly  diagnosed acute myeloid leukaemia (aml) who are ineligible for intensive chemotherapy.