Alecensa 150 mg Hartkapseln Švicarska - njemački - Swissmedic (Swiss Agency for Therapeutic Products)

alecensa 150 mg hartkapseln

roche pharma (schweiz) ag - alectinibum - hartkapseln - alectinibum 150 mg ut alectinibi hydrochloridum, lactosum monohydricum 33.67 mg, hydroxypropylcellulosum, natrii laurilsulfas corresp. natrium 6 mg, carmellosum calcicum, magnesii stearas, kapselhülle: carrageenanum, kalii chloridum, e 171, cera carnauba, maydis amylum, hypromellosum, drucktinte: e 172 (rubrum), e 172 (flavum), e 132, cera carnauba, lacca, polyglyceroli-3 mono-oleas, pro capsula. - nicht-kleinzelliges lungenkarzinom (nsclc) - synthetika

Tagrisso 40 mg Filmtabletten Švicarska - njemački - Swissmedic (Swiss Agency for Therapeutic Products)

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 Švicarska - njemački - Swissmedic (Swiss Agency for Therapeutic Products)

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

Alecensa Europska Unija - njemački - EMA (European Medicines Agency)

alecensa

roche registration gmbh - alectinibhydrochlorid - karzinom, nicht kleinzellige lunge - antineoplastische mittel - alecensa als monotherapie ist indiziert für die erstlinienbehandlung von erwachsenen patienten mit anaplastischem lymphomkinase (alk) -positivem fortgeschrittenem nicht-kleinzelligem lungenkrebs (nsclc). alecensa als monotherapie ist indiziert für die behandlung von erwachsenen patienten mit alk‑positivem fortgeschrittenem nicht-kleinzelligem lungenkrebs behandelt, die zuvor mit crizotinib.

Tagrisso Europska Unija - njemački - EMA (European Medicines Agency)

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.

Lorviqua Europska Unija - njemački - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - karzinom, nicht kleinzellige lunge - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Lumeblue (previously known as Methylthioninium chloride Cosmo) Europska Unija - njemački - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - methylthioniniumchlorid - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Carboplatin onkovis 10 mg/ml Infusionslösung Njemačka - njemački - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

carboplatin onkovis 10 mg/ml infusionslösung

onkovis gmbh (8111905) - carboplatin - infusionslösung - teil 1 - infusionslösung; carboplatin (23168) 50 milligramm

Zejula Europska Unija - njemački - EMA (European Medicines Agency)

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.