Europeiska unionen - svenska - EMA (European Medicines Agency)

mabxience research sl - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiska medel - alymsys in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. alymsys in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. alymsys in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with alymsys in combination with capecitabine. alymsys, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. alymsys, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations. alymsys in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. alymsys, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer. alymsys, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents. alymsys, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents. alymsys, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix.

Europeiska unionen - svenska - EMA (European Medicines Agency)

eli lilly nederland b.v. - drotrecogin alfa (aktiverad) - sepsis; multiple organ failure - antitrombotiska medel - xigris är indicerat för behandling av vuxna patienter med svår sepsis med multipel organsvikt när tillägg till bästa standardbehandling. användning av xigris övervägas främst i situationer när behandling kan påbörjas inom 24 timmar efter debuten av organsvikt (för ytterligare information se avsnitt 5.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

g.l. pharma gmbh - febuxostathemihydrat - filmdragerad tablett - 120 mg - mannitol hjälpämne; natriumlaurilsulfat hjälpämne; febuxostathemihydrat 123,42 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

elpen pharmaceutical co. inc - flutikasonpropionat - inhalationspulver, avdelad dos - 250 mikrogram/dos - flutikasonpropionat 250 mikrog aktiv substans; laktosmonohydrat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

elpen pharmaceutical co. inc - flutikasonpropionat - inhalationspulver, avdelad dos - 500 mikrogram/dos - flutikasonpropionat 500 mikrog aktiv substans; laktosmonohydrat hjälpämne

Europeiska unionen - svenska - EMA (European Medicines Agency)

novartis europharm limited - basiliximab - graft rejection; kidney transplantation - immunsuppressiva - simulect är indicerat för profylax av akut organavstötning vid de-novo allogen renaltransplantation hos vuxna och barn (1-17 år). det används tillsammans med ciklosporin för microemulsion - och kortikosteroid-baserade immunosuppression, i patienter med panel reaktiv antikroppar mindre än 80%, eller i en trippel underhåll immunosuppressiva regim som innehåller ciklosporin för microemulsion, kortikosteroider och antingen azatioprin eller mykofenolatmofetil.

Europeiska unionen - svenska - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunsuppressiva - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

bluefish pharmaceuticals ab - sorafenibtosilat - filmdragerad tablett - 200 mg - sorafenibtosilat 274 mg aktiv substans; natriumlaurilsulfat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orion corporation - kaspofunginacetat - pulver till koncentrat till infusionsvätska, lösning - 70 mg - sackaros hjälpämne; mannitol hjälpämne; kaspofunginacetat 77,69 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orion corporation - kaspofunginacetat - pulver till koncentrat till infusionsvätska, lösning - 50 mg - mannitol hjälpämne; sackaros hjälpämne; kaspofunginacetat 55,52 mg aktiv substans