Suomi - suomi - Fimea (Suomen lääkevirasto)

pch pharmachemie bv - fludarabini phosphas - injektio/infuusiokonsentraatti, liuosta varten - 25 mg/ml - fludarabiini

Euroopan unioni - suomi - EMA (European Medicines Agency)

norgine b.v. - ferri maltolia - anemia, raudanvajaus - antianemiset valmisteet - feraccru on tarkoitettu aikuisten hoitoon raudanpuute.

Euroopan unioni - suomi - EMA (European Medicines Agency)

theravia - hydroksikarbamidi - anemia, sickle cell - antineoplastiset aineet - siklos on tarkoitettu toistuvien kivuliaita verisuonten tukkeutumisen aiheuttamia kriisitilanteita mukaan lukien akuutti rinnassa oireyhtymä lapsilla ja aikuisilla potilailla, jotka kärsivät oireista sirppi-solun oireyhtymä.

Euroopan unioni - suomi - EMA (European Medicines Agency)

nova laboratories ireland limited - hydroksikarbamidi - anemia, sickle cell - antineoplastiset aineet - ehkäisy vaso-okklusiiviseen komplikaatioita sirppisoluanemia potilailla, jotka olivat yli 2-vuotiaille.

Euroopan unioni - suomi - EMA (European Medicines Agency)

roche registration gmbh - metoksipolyetyleeniglykoliepoetiini beeta - anemia; kidney failure, chronic - antianemiset valmisteet - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Euroopan unioni - suomi - EMA (European Medicines Agency)

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - muut anemialääkkeet - reblozyl is indicated for the treatment of adult patients with transfusion-dependent anaemia due to very low, low and intermediate-risk myelodysplastic syndromes (mds) with ring sideroblasts, who had an unsatisfactory response to or are ineligible for erythropoietin-based therapy (see section 5. reblozyl is indicated in adults for the treatment of anaemia associated with transfusion dependent and non transfusion dependent beta thalassaemia (see section 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

oncopeptides ab - melphalan flufenamide hydrochloride - multiple myeloma - antineoplastiset aineet - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Euroopan unioni - suomi - EMA (European Medicines Agency)

substipharm - prasugreeli - acute coronary syndrome; angina, unstable; myocardial infarction - antitromboottiset aineet - efient, yhteistyössä annostella asetyylisalisyylihappo (asa) on tarkoitettu ehkäisy atherothrombotic tapahtumista potilailla sepelvaltimotautikohtaus (i. epästabiili angina pectoris, ei st-segmentin nousua sydäninfarkti [ua / nstemi] tai st-segmentin nousua sydäninfarkti [stemi]) käynnissä ensisijainen tai viivästynyt perkutaaninen sepelvaltimotoimenpide (pci).

Euroopan unioni - suomi - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - multiple myeloma - antineoplastiset aineet - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.