Abstral Tungurótartafla 100 míkróg Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 100 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 100 míkróg

Fentanyl Actavis Forðaplástur 100 míkróg/klst. Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

fentanyl actavis forðaplástur 100 míkróg/klst.

actavis group ptc ehf. - fentanylum inn - forðaplástur - 100 míkróg/klst.

Fentanyl Actavis Forðaplástur 25 míkróg/klst. Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

fentanyl actavis forðaplástur 25 míkróg/klst.

actavis group ptc ehf. - fentanylum inn - forðaplástur - 25 míkróg/klst.

Fentanyl Actavis Forðaplástur 50 míkróg/klst. Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

fentanyl actavis forðaplástur 50 míkróg/klst.

actavis group ptc ehf. - fentanylum inn - forðaplástur - 50 míkróg/klst.

Fentanyl Actavis Forðaplástur 75 míkróg/klst. Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

fentanyl actavis forðaplástur 75 míkróg/klst.

actavis group ptc ehf. - fentanylum inn - forðaplástur - 75 míkróg/klst.

Tecentriq Den europeiske union - islandsk - EMA (European Medicines Agency)

tecentriq

roche registration gmbh - atezolizumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - Æxlishemjandi lyf - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq eitt og sér er ætlað fyrir meðferð fullorðinn sjúklinga með staðnum háþróaður eða sjúklingum nsclc eftir áður en lyfjameðferð. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq eitt og sér er ætlað fyrir meðferð fullorðinn sjúklinga með staðnum háþróaður eða sjúklingum nsclc eftir áður en lyfjameðferð. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.