Swedia - Swedia - Läkemedelsverket (Medical Products Agency)

baxter medical ab - dl-metionin; alanin; arginin; fenylalanin; fiskolja, rik på omega-3-syror; glukosmonohydrat; glycin; histidin; isoleucin; kalciumkloriddihydrat; kaliumklorid; leucin; lysinhydroklorid; magnesiumsulfatheptahydrat; natriumacetattrihydrat; natriumglycerofosfat, hydratiserat; olivolja, raffinerad; prolin; serin; sojaolja, raffinerad; treonin; triglycerider, medellångkedjiga; tryptofan; tyrosin; valin; zinksulfatheptahydrat - infusionsvätska, emulsion - arginin 11,5 mg aktiv substans; isoleucin 6 mg aktiv substans; histidin 4,8 mg aktiv substans; prolin 6,8 mg aktiv substans; tryptofan 1,8 mg aktiv substans; treonin 4,2 mg aktiv substans; valin 5,8 mg aktiv substans; fenylalanin 5,6 mg aktiv substans; leucin 7,3 mg aktiv substans; dl-metionin 4 mg aktiv substans; serin 5 mg aktiv substans; lysinhydroklorid 7,25 mg aktiv substans; glukosmonohydrat 462 mg aktiv substans; fiskolja, rik på omega-3-syror 40 mg aktiv substans; olivolja, raffinerad 50 mg aktiv substans; sojaolja, raffinerad 60 mg aktiv substans; triglycerider, medellångkedjiga 50 mg aktiv substans; glycerol hjälpämne; natriumglycerofosfat, hydratiserat 5,92 mg aktiv substans; tyrosin 0,4 mg aktiv substans; kaliumklorid 4,48 mg aktiv substans; zinksulfatheptahydrat 0,023 mg aktiv substans; magnesiumsulfatheptahydrat 2,47 mg aktiv substans; kalciumkloriddihydrat 0,74 mg aktiv substans; natriumacetattrihydrat 5,62 mg aktiv substans; glycin 10,3 mg aktiv substans; alanin 20,7 mg aktiv substans

Uni Eropa - Swedia - EMA (European Medicines Agency)

blueprint medicines (netherlands) b.v. - avapritinib - gastrointestinala stromaltumörer - andra antineoplastiska medel, protein kinas-hämmare - ayvakyt is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (gist) harbouring the platelet-derived growth factor receptor alpha (pdgfra) d842v mutation.

Finlandia - Swedia - Ecolab

ecolab deutschland gmbh -

Finlandia - Swedia - Ecolab

ecolab deutschland gmbh -

Uni Eropa - Swedia - EMA (European Medicines Agency)

amicus therapeutics europe limited - miglustat - glykogenlagringssjukdomstyp ii - andra matsmältningsvägar och metabolismprodukter - opfolda (miglustat) is an enzyme stabiliser of cipaglucosidase alfa long-term enzyme replacement therapy in adults with late-onset pompe disease (acid α- glucosidase [gaa] deficiency).

Uni Eropa - Swedia - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a. - velmanase alfa - alpha-mannosidosis - andra matsmältningsorgan och ämnesomsättning produkter, - behandling av icke-neurologiska manifestationer hos patienter med mild till måttlig alpha-mannosidosis.

Uni Eropa - Swedia - EMA (European Medicines Agency)

accord healthcare s.l.u. - imatinib - precursor cell lymphoblastic leukemia-lymphoma; dermatofibrosarcoma; myelodysplastic-myeloproliferative diseases; leukemia, myelogenous, chronic, bcr-abl positive; hypereosinophilic syndrome - imatinib - imatinib accord is indicated for the treatment of- adult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. - adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. - adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. - adult patients with relapsed or refractory ph+ all as monotherapy. - adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. - adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. - adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. - the treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). - the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. patients who have a low or very low risk of recurrence should not receive adjuvant treatmentthe effect of imatinib on the outcome of bone marrow transplantation has not been determined. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic dfsp. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. förutom vid nyligen diagnostiserad kml kronisk fas, det finns inga kontrollerade studier som visar på en klinisk nytta eller ökad överlevnad för dessa sjukdomar. .

Swedia - Swedia - Läkemedelsverket (Medical Products Agency)

abigo medical ab - all-rac-alfa-tokoferylacetat; askorbinsyra; cyanokobalamin; folsyrahydrat; järn(ii)fumarat; kolekalciferol; natriumaskorbat; nikotinamid; pyridoxinhydroklorid; retinolacetat; riboflavin; tiaminnitrat - tablett - järn(ii)fumarat 57,2 mg aktiv substans; retinolacetat 0,9 mg aktiv substans; all-rac-alfa-tokoferylacetat 9 mg aktiv substans; sackaros hjälpämne; mannitol hjälpämne; butylhydroxitoluen hjälpämne; tiaminnitrat 1,2 mg aktiv substans; nikotinamid 16 mg aktiv substans; riboflavin 1,4 mg aktiv substans; cyanokobalamin 3 mikrog aktiv substans; kolekalciferol 5 mikrog aktiv substans; folsyrahydrat 0,4 mg aktiv substans; pyridoxinhydroklorid 2,1 mg aktiv substans; askorbinsyra 19,8 mg aktiv substans; natriumaskorbat 45,2 mg aktiv substans - multivitaminer och järn

Swedia - Swedia - Läkemedelsverket (Medical Products Agency)

baxter medical ab - all-rac-alfa-tokoferol ; askorbinsyra; biotin; cyanokobalamin; dexpantenol; folsyrahydrat; kokarboxylastetrahydrat; kolekalciferol; nikotinamid; pyridoxinhydroklorid; retinolpalmitat; riboflavinnatriumfosfat - pulver till injektions-/infusionsvätska, lösning - sojalecitin hjälpämne; kokarboxylastetrahydrat 5,8 mg aktiv substans; riboflavinnatriumfosfat 5,67 mg aktiv substans; dexpantenol 16,15 mg aktiv substans; cyanokobalamin 6 mikrog aktiv substans; all-rac-alfa-tokoferol 10,2 mg aktiv substans; askorbinsyra 125 mg aktiv substans; nikotinamid 46 mg aktiv substans; retinolpalmitat 3500 ie aktiv substans; kolekalciferol 220 ie aktiv substans; pyridoxinhydroklorid 5,5 mg aktiv substans; folsyrahydrat 414 mikrog aktiv substans; biotin 69 mikrog aktiv substans - vitaminer

Swedia - Swedia - Läkemedelsverket (Medical Products Agency)

pharmaxim ab - all-rac-alfa-tokoferylacetat; natriumselenit, vattenfri - granulat - 30 mg/g+0,6 mg/g - natriumselenit, vattenfri 1,32 mg aktiv substans; butylhydroxitoluen hjälpämne; sackaros hjälpämne; all-rac-alfa-tokoferylacetat 30 mg aktiv substans - kombinationer - får, häst, nöt, svin