Europäische Union - Deutsch - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastische mittel - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. relative to nivolumab monotherapy, an increase in progression-free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression (see sections 4. 4 und 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%.

Europäische Union - Deutsch - EMA (European Medicines Agency)

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.

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - lorlatinibum - filmtabletten - lorlatinibum 25 mg, cellulosum microcristallinum, calcii hydrogenophosphas dihydricus, carboxymethylamylum natricum a corresp. natrium 0.315 mg, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 1.575 mg, macrogolum 4000, triacetinum, e 171, e 172 (nigrum), e 172 (rubrum), pro compresso obducto. - nicht kleinzelliges lungenkarzinom (non small cell lung cancer, nsclc) - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - lorlatinibum - filmtabletten - lorlatinibum 100 mg, cellulosum microcristallinum, calcii hydrogenophosphas dihydricus, carboxymethylamylum natricum a corresp. natrium 0.84 mg, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 4.2 mg, macrogolum 4000, triacetinum, e 171, e 172 (nigrum), e 172 (rubrum), pro compresso obducto. - nicht kleinzelliges lungenkarzinom (non small cell lung cancer, nsclc) - synthetika

Europäische Union - Deutsch - EMA (European Medicines Agency)

amgen europe bv - sotorasib - karzinom, nicht kleinzellige lunge - antineoplastische mittel - lumykras as monotherapy is indicated for the treatment of adults with advanced non-small cell lung cancer (nsclc) with kras g12c mutation and who have progressed after at least one prior line of systemic therapy.

Europäische Union - Deutsch - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - karzinom, nicht kleinzellige lunge - antineoplastische mittel - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

alnylam switzerland gmbh - vutrisiranum natricum - injektionslösung in einer fertigspritze - suspension: vutrisiranum natricum 25 mg pro dosi, natrii dihydrogenophosphas dihydricus, dinatrii phosphas dihydricus, natrii chloridum, aqua ad iniectabile, acidum phosphoricum, natrii hydroxidum, pro praeparatione, natrium < 23 mg/ml. - amvuttra wird zur behandlung der hereditären transthyretin-amyloidose (hattr-amyloidose) bei erwachsenen patienten mit polyneuropathie der stadien 1 oder 2 angewendet - transplantat: gentherapieprodukt

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

aqvida gmbh (8135745) - azathioprin - filmtablette - teil 1 - filmtablette; azathioprin (04347) 25 milligramm

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

aqvida gmbh (8135745) - azathioprin - filmtablette - teil 1 - filmtablette; azathioprin (04347) 50 milligramm

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

zentiva pharma gmbh (8075753) - methylphenidathydrochlorid - hartkapsel mit veränderter wirkstofffreisetzung - 60 mg - teil 1 - hartkapsel mit veränderter wirkstofffreisetzung; methylphenidathydrochlorid (06085) 60 milligramm