tagrisso
astrazeneca ab - osimertinib mesilate - karzinom, nicht kleinzellige lunge - andere antineoplastische wirkstoffe, die protein-kinase-inhibitoren - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.
tagrisso 40 mg filmtabletten
astrazeneca ag - osimertinibum - filmtabletten - osimertinibum 40 mg ut osimertinibi mesilas 47.7 mg, mannitolum 147 mg, cellulosum microcristallinum, hydroxypropylcellulosum substitutum humile, natrii stearylis fumaras corresp. natrium 0.3 mg, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (flavum), e 172 (rubrum), e 172 (nigrum), pro compresso obducto. - nicht-kleinzelliges lungenkarzinom - synthetika
tagrisso 80 mg filmtabletten
astrazeneca ag - osimertinibum - filmtabletten - osimertinibum 80 mg ut osimertinibi mesilas 95.4 mg, mannitolum 295 mg, cellulosum microcristallinum, hydroxypropylcellulosum substitutum humile, natrii stearylis fumaras corresp. natrium 0.6 mg, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (flavum), e 172 (rubrum), e 172 (nigrum), pro compresso obducto. - nicht-kleinzelliges lungenkarzinom - synthetika
carboplatin onkovis 10 mg/ml infusionslösung
onkovis gmbh (8111905) - carboplatin - infusionslösung - teil 1 - infusionslösung; carboplatin (23168) 50 milligramm
zejula
glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - antineoplastische mittel - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.
mekinist
novartis europharm limited - trametinib - melanom - antineoplastische mittel - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 und 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. non-small cell lung cancer (nsclc)in kombination mit trametinib dabrafenib ist angezeigt zur behandlung von erwachsenen patienten mit fortgeschrittenem nicht-kleinzelligem lungenkrebs mit einer braf-v600-mutation.
tafinlar
novartis europharm limited - dabrafenib mesilate - melanom - antineoplastische mittel - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 und 5. adjuvante behandlung von melanomadabrafenib in kombination mit trametinib ist angezeigt für die adjuvante behandlung von erwachsenen patienten mit stadium iii melanom mit einer braf-v600 mutation, die nach vollständiger resektion. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.
mekinist 0.5mg filmtabletten
novartis pharma schweiz ag - trametinibum - filmtabletten - trametinibum 0.5 mg ut trametinibi dimethylis sulfoxidi solvatum, mannitolum, cellulosum microcristallinum, hypromellosum, carmellosum natricum conexum, natrii laurilsulfas, silica colloidalis hydrica, magnesii stearas, Überzug: hypromellosum, macrogolum, e 171, e 172 (flavum), pro compresso obducto corresp. natrium 0.199 mg. - melanom, nicht-kleinzelliges lungenkarzinom - synthetika
mekinist 2mg filmtabletten
novartis pharma schweiz ag - trametinibum - filmtabletten - trametinibum 2 mg ut trametinibi dimethylis sulfoxidi solvatum, mannitolum, cellulosum microcristallinum, hypromellosum, carmellosum natricum conexum, natrii laurilsulfas, silica colloidalis hydrica, magnesii stearas, Überzug: hypromellosum, macrogolum, polysorbatum 80, e 171, e 172 (rubrum), pro compresso obducto corresp. natrium 0.232 mg. - melanom, nicht-kleinzelliges lungenkarzinom - synthetika
cotellic 20mg filmtabletten
roche pharma (schweiz) ag - cobimetinibum - filmtabletten - cobimetinibum 20 mg ut cobimetinibi hemifumaras, cellulosum microcristallinum, lactosum monohydricum 36.48 mg, carmellosum natricum conexum corresp. natrium max. 0.99 mg, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, pro compresso obducto. - onkologikum - synthetika