etoposid fresenius kabi 20 mg/ml infuusiokonsentraatti, liuosta varten
fresenius kabi ab - etoposide - infuusiokonsentraatti, liuosta varten - 20 mg/ml - etoposidi
etoposid hospira 20 mg/ml infuusiokonsentraatti, liuosta varten
hospira - etoposidum - infuusiokonsentraatti, liuosta varten - 20 mg/ml - etoposidi
etoposide accord 20 mg/ml infuusiokonsentraatti, liuosta varten
accord healthcare b.v. - etoposide - infuusiokonsentraatti, liuosta varten - 20 mg/ml - etoposidi
etoposide pfizer 20 mg/ml infuusiokonsentraatti, liuosta varten
pfizer oy - etoposide - infuusiokonsentraatti, liuosta varten - 20 mg/ml - etoposidi
vepesid 50 mg kapseli, pehmeä
cheplapharm arzneimittel gmbh - etoposide - kapseli, pehmeä - 50 mg - etoposidi
malarone 250 mg / 100 mg tabletti, kalvopäällysteinen
glaxosmithkline oy - atovaquone, proguanil hydrochloride - tabletti, kalvopäällysteinen - 250 mg / 100 mg - proguaniili ja atovakvoni
rumbabor 62.5 mg / 25 mg tabletti, kalvopäällysteinen
sandoz a/s sandoz a/s - atovaquonum,proguanili hydrochloridum - tabletti, kalvopäällysteinen - 62.5 mg / 25 mg - proguaniili, yhdistelmävalmisteet
rumbabor 250 mg / 100 mg tabletti, kalvopäällysteinen
sandoz a/s sandoz a/s - atovaquonum,proguanili hydrochloridum - tabletti, kalvopäällysteinen - 250 mg / 100 mg - proguaniili, yhdistelmävalmisteet
atovaquone/proguanil glenmark 250 mg / 100 mg tabletti, kalvopäällysteinen
glenmark arzneimittel gmbh - proguanili hydrochloridum,atovaquonum - tabletti, kalvopäällysteinen - 250 mg / 100 mg - proguaniili, yhdistelmävalmisteet
tecentriq
roche registration gmbh - atezolizumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - antineoplastiset aineet - 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 monoterapiana on tarkoitettu aikuisille potilaille, joilla on paikallisesti pitkälle edennyt tai metastaattinen ei-pienisoluinen keuhkosyöpä aikaisemman kemoterapian jälkeen. 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 monoterapiana on tarkoitettu aikuisille potilaille, joilla on paikallisesti pitkälle edennyt tai metastaattinen ei-pienisoluinen keuhkosyöpä aikaisemman kemoterapian jälkeen. 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.