Evrópusambandið - íslenska - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ozanimod stutt og long-term - multiple sclerosis, relapsing-remitting; colitis, ulcerative - Ónæmisbælandi lyf - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

astrazeneca ab - dapagliflozin própandiolól einhýdrat - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - lyf notuð við sykursýki - type 2 diabetes mellitusedistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. auk þess önnur lyf fyrir meðferð tegund sykursýki 2. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 og 5. heart failureedistride is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseedistride is indicated in adults for the treatment of chronic kidney disease.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

astrazeneca ab - dapagliflozin própandiolól einhýdrat - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - lyf notuð við sykursýki - type 2 diabetes mellitusforxiga is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. auk þess önnur lyf fyrir meðferð tegund sykursýki 2. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 og 5. heart failureforxiga is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseforxiga is indicated in adults for the treatment of chronic kidney disease.

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 50 mg

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 300 mg

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 200 mg

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 150 mg

Evrópusambandið - íslenska - EMA (European Medicines Agency)

astra zeneca ab - saxagliptin, dapagliflozin propanediol einhýdrat - diabetes mellitus, type 2; diabetes mellitus; nutritional and metabolic diseases; metabolic diseases; glucose metabolism disorders - lyf notuð við sykursýki - qtern, fastur skammt sambland af saxagliptin og dapagliflozin, er ætlað í fullorðnir 18 ára og eldri með tegund sykursýki 2:til að bæta blóðsykursstjórnun þegar sjúklingar og/eða sulphonylurea (su) og einn af monocomponents af qtern veita ekki fullnægjandi blóðsykursstjórnun,þegar þegar í meðferð með frjáls sambland af dapagliflozin og saxagliptin. (sjá kafla 4. 2, 4. 4, 4. 5 og 5. 1 fyrir boði gögn um sturtu rannsakað.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

genzyme europe bv - sevelamer hýdróklóríð - hyperphosphatemia; renal dialysis - Öll önnur lækningavörur - tasermity er ætlað til að stjórna blóðfosfathækkun hjá fullorðnum sjúklingum sem fá blóðskilun eða kviðskilun. sevelamer stutt og long-term ætti að vera notuð í samhengi margar læknlngar, sem gæti verið kalk, 1,25 dihydroxy d3 vítamín eða einn af hliðstæðum til að stjórna þróun skert beinum.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glycogen geymsluskammt tegund ii - Önnur meltingarvegi og efnaskipti vörur, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).