Sutent Evrópusambandið - íslenska - EMA (European Medicines Agency)

sutent

pfizer limited - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - Æxlishemjandi lyf - gastrointestinal stromal tumour (gist)sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. experience with sutent as first-line treatment is limited (see section 5.

Sunitinib Accord Evrópusambandið - íslenska - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - Æxlishemjandi lyf - 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.

SomaKit TOC Evrópusambandið - íslenska - EMA (European Medicines Agency)

somakit toc

advanced accelerator applications - edotreótíð - neuroendocrine tumors; radionuclide imaging - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. eftir radiolabelling með gallín (68ga) i lausn, lausn gallín (68ga) edotreotide fæst er ætlað fyrir sneiðmyndatöku losun höfði (gÆludÝr) hugsanlegur somatostatini viðtaka yfirtjáningu í fullorðinn sjúklinga með staðfest eða grun vel þroskað maga-enteropancreatic taugakirtilsuppruna æxli (gep-hrein) fyrir localizing aðal æxli og þeirra meinvörp.

Sandostatin Stungulyf, lausn 100 míkróg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sandostatin stungulyf, lausn 100 míkróg/ml

novartis healthcare a/s - octreotidum inn - stungulyf, lausn - 100 míkróg/ml

Sandostatin Stungulyf, lausn 50 míkróg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sandostatin stungulyf, lausn 50 míkróg/ml

novartis healthcare a/s - octreotidum inn - stungulyf, lausn - 50 míkróg/ml

Sandostatin LAR Stungulyfsstofn og leysir, dreifa 10 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sandostatin lar stungulyfsstofn og leysir, dreifa 10 mg

novartis healthcare a/s - octreotidum inn - stungulyfsstofn og leysir, dreifa - 10 mg

Sandostatin LAR Stungulyfsstofn og leysir, dreifa 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sandostatin lar stungulyfsstofn og leysir, dreifa 20 mg

novartis healthcare a/s - octreotidum inn - stungulyfsstofn og leysir, dreifa - 20 mg