Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

b. braun melsungen ag - ibuprofen - infusionsvæske, opløsning - 200 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

accord healthcare s.l.u. - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastiske midler - azacitidine accord er indiceret til behandling af voksne patienter, der ikke er berettiget til hæmatopoietisk stamcelle transplantation (hsct) med:- intermediær-2 og højrisiko myelodysplastisk syndrom (mds) i henhold til international prognostic scoring system (ipss),- kronisk myelomonocytisk leukæmi (cmml) med 10-29 % marv blaster uden myeloproliferative lidelse,- akut myeloid leukæmi (aml) med 20-30 % blaster og multi-slægt dysplasi, ifølge world health organisation (who) klassifikation,- aml med >30% marv blaster i henhold til who-klassifikationen.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sandoz a/s - azacitidin - pulver til injektionsvæske, suspension - 25 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - azacitidin - pulver til injektionsvæske, suspension - 25 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

zentiva k.s. - azacitidin - pulver til injektionsvæske, suspension - 25 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

zentiva k.s. - sunitinib - kapsler, hårde - 12,5 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

accord healthcare s.l.u. - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastiske midler - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

krka d.d. novo mesto - sunitinibmalat - kapsler, hårde - 12,5 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - narkotika anvendt i diabetes - type 2 diabetes mellitusdapagliflozin viatris 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 exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. 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 failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

accord healthcare s.l.u. - voriconazol - aspergillosis; candidiasis; mycoses - antimykotika til systemisk brug, triazol-derivater - voriconazol, er et bredt spektrum, triazol-svampemidler agent og er indiceret hos voksne og børn på to år og derover, som følger:behandling af invasiv aspergillosis;behandling af candidaemia i ikke-neutropenic patienter, behandling af fluconazol-resistente alvorlige invasive candida infektioner (herunder c. krusei);behandling af alvorlige svampeinfektioner forårsaget af scedosporium spp.. og fusarium spp.. voriconazol overenskomst bør administreres primært til patienter med progressive, eventuelt livstruende infektioner.