ノルウェー - ノルウェー語 - Statens legemiddelverk

b. braun melsungen ag - glukosemonohydrat / natriumdihydrogenfosfatdihydrat / sinkacetatdihydrat / soyaolje, renset / triglyserider av middels kjedelengde / isoleucin / leucin / lysinhydroklorid / metionin / fenylalanin / treonin / tryptofan / valin / arginin / histidinhydrokloridmonohydrat / alanin / aspartinsyre / glutaminsyre / glysin / prolin / serin / natriumhydroksid / natriumklorid / natriumacetattrihydrat / kaliumacetat / magnesiumacetattetrahydrat / kalsiumkloriddihydrat - infusjonsvæske, emulsjon - 144 mg/ ml / 2.496 mg/ ml / 0.007 mg/ ml / 20 mg/ ml / 20 mg/ ml / 3.284 mg/ ml / 4.384 mg/ ml / 3.186 mg/ ml / 2.736 mg/ ml / 4.916 mg/ ml / 2.54 mg/ ml / 0.8 mg/ ml / 3.604 mg/ ml / 3.78 mg/ ml / 1.753 mg/ ml / 6.792 mg/ ml / 2.1 mg/ ml / 4.908 mg/ ml / 2.312 mg/ ml / 4.76 mg/ ml / 4.2 mg/ ml / 1.171 mg/ ml / 0.378 mg/ ml / 0.25 mg/ ml / 3.689 mg/ ml / 0.91 mg/ ml / 0.623 mg/ ml

ノルウェー - ノルウェー語 - Statens legemiddelverk

b. braun melsungen ag - glukosemonohydrat / natriumfosfatdihydrat / sinkacetatdihydrat / triglyserider av middels kjedelengde / soyaolje, renset / omega-3-syretriglyserider / isoleucin / leucin / lysinhydroklorid / metionin / fenylalanin / treonin / tryptofan / valin / arginin / histidinhydrokloridmonohydrat / alanin / aspartinsyre / glutaminsyre / glysin / prolin / serin / natriumhydroksid / natriumklorid / natriumacetattrihydrat / kaliumacetat / magnesiumacetattetrahydrat / kalsiumkloriddihydrat - infusjonsvæske, emulsjon

欧州連合 - ノルウェー語 - EMA (European Medicines Agency)

astrazeneca ab - andexanet alfa - narkotika-relaterte bivirkninger og uønskede reaksjoner - alle andre terapeutiske produkter - for voksne pasienter behandlet med en direkte faktor xa (anl) inhibitor (apixaban eller rivaroxaban) når reversering av antikoagulasjonsbehandling er nødvendig på grunn av livstruende eller ukontrollert blødning.

ノルウェー - ノルウェー語 - Statens legemiddelverk

pfizer as - diltiazemhydroklorid - depottablett - 180 mg

ノルウェー - ノルウェー語 - Statens legemiddelverk

pfizer as - diltiazemhydroklorid - depottablett - 240 mg

ノルウェー - ノルウェー語 - Statens legemiddelverk

pfizer as - diltiazemhydroklorid - depottablett - 300 mg

ノルウェー - ノルウェー語 - Statens legemiddelverk

b. braun melsungen ag - glukosemonohydrat / soyaolje, renset / aminosyrer, uspesifisert - infusjonsvæske, emulsjon

ノルウェー - ノルウェー語 - Statens legemiddelverk

sintetica gmbh - noradrenalintartrat - konsentrat til infusjonsvæske, oppløsning - 1 mg/ ml

ノルウェー - ノルウェー語 - Statens legemiddelverk

dr. loges + co. gmbh - djevelklorot - tablett, filmdrasjert

欧州連合 - ノルウェー語 - EMA (European Medicines Agency)

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - antineoplastiske midler - imatinib koanaa is indicated for the treatment ofadult 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. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe 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. pasienter som har en lav eller svært lav risiko for tilbakefall bør ikke får adjuvant behandling. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. 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 gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. bortsett fra i nydiagnostisert kronisk fase kml, det er ingen kontrollerte studier som viser en klinisk nytte eller økt overlevelse for disse sykdommer.