Yervoy Euroopa Liit - saksa - EMA (European Medicines Agency)

yervoy

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%.

LAPTOVET PULVIS N Pulver Saksamaa - saksa - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

laptovet pulvis n pulver

atarost allg.tierarzneimittel-fabrik dr.u.böhmer nachf.gmbh & co. - ethacridinlactat-monohydrat, calciumhydrogenphosphat-dihydrat, eisen(ii)-sulfat-heptahydrat, mangan(ii)-chlorid 4 h<2>o, kupfer(ii)-sulfat-pentahydrat, cobalt(ii)-d-gluconat 2 h<2>o, niccolum carbonicum (pot.-angaben) - pulver - ethacridinlactat-monohydrat 50.mg; calciumhydrogenphosphat-dihydrat 9.g; eisen(ii)-sulfat-heptahydrat 89.785g; mangan(ii)-chlorid 4 h<2>o 5.mg; kupfer(ii)-sulfat-pentahydrat 1.g; cobalt(ii)-d-gluconat 2 h<2>o 5.mg; niccolum carbonicum (pot.-angaben) 5.mg

Molybdän compositum Tablette Saksamaa - saksa - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

molybdän compositum tablette

biologische heilmittel heel gmbh - sulfur (pot.-angaben), phosphorus (pot.-angaben), cuprum sulfuricum (pot.-angaben), cerium oxalicum (pot.-angaben), ferrum fumaricum (pot.-angaben), manganum gluconicum (pot.-angaben), zincum gluconicum (pot.-angaben), magnesium asparticum (pot.-angaben), natrium molybdaenicum (pot.-angaben), cobaltum gluconicum (pot.-angaben), kalium asparaginicum (pot.-angaben), niccolum aceticum (pot.-angaben), rubidium chloratum (pot.-angaben) - tablette - sulfur (pot.-angaben) 3.mg; phosphorus (pot.-angaben) 3.mg; cuprum sulfuricum (pot.-angaben) 3.mg; cerium oxalicum (pot.-angaben) 3.mg; ferrum fumaricum (pot.-angaben) 3.mg; manganum gluconicum (pot.-angaben) 3.mg; zincum gluconicum (pot.-angaben) 3.mg; magnesium asparticum (pot.-angaben) 3.mg; natrium molybdaenicum (pot.-angaben) 15.mg; cobaltum gluconicum (pot.-angaben) 3.mg; kalium asparaginicum (pot.-angaben) 3.mg; niccolum aceticum (pot.-angaben) 3.mg; rubidium chloratum (pot.-angaben) 3.mg

Cabometyx Euroopa Liit - saksa - EMA (European Medicines Agency)

cabometyx

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - antineoplastische mittel - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.

NUXVOMICA-SELOPLEX Saksamaa - saksa - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

nuxvomica-seloplex

marien-apotheke josef duschl (0078597) - kalium iodatum (pot.-angaben); strychnos nux-vomica (pot.-angaben); phosphorus (pot.-angaben); cuprum arsenicosum (pot.-angaben); niccolum metallicum (pot.-angaben) - tropfen - kalium iodatum (pot.-angaben) (1974) 2,5 milliliter; strychnos nux-vomica (pot.-angaben) (1990) 2 milliliter; phosphorus (pot.-angaben) (2015) 1,5 milliliter; cuprum arsenicosum (pot.-angaben) (6146) 1,5 milliliter; niccolum metallicum (pot.-angaben) (14998) 2,5 milliliter

YERVOY 50 mg/10 ml Konzentrat zur Herstellung einer Infusionslösung Šveits - saksa - Swissmedic (Swiss Agency for Therapeutic Products)

yervoy 50 mg/10 ml konzentrat zur herstellung einer infusionslösung

bristol-myers squibb sa - ipilimumabum - konzentrat zur herstellung einer infusionslösung - ipilimumabum 50 mg, trometamoli hydrochloridum, natrii chloridum, mannitolum, acidum penteticum, polysorbatum 80, natrii hydroxidum aut acidum hydrochloridum, aqua ad iniectabile q.s. ad solutionem pro 10 ml corresp. natrium 23 mg. - melanom, nierenzellkarzinom, kolorektales karzinom - biotechnologika

YERVOY 200 mg/40 ml Konzentrat zur Herstellung einer Infusionslösung Šveits - saksa - Swissmedic (Swiss Agency for Therapeutic Products)

yervoy 200 mg/40 ml konzentrat zur herstellung einer infusionslösung

bristol-myers squibb sa - ipilimumabum - konzentrat zur herstellung einer infusionslösung - ipilimumabum 200 mg, trometamoli hydrochloridum, natrii chloridum, mannitolum, acidum penteticum, polysorbatum 80, natrii hydroxidum aut acidum hydrochloridum, aqua ad iniectabile q.s. ad solutionem pro 40 ml corresp. natrium 92 mg. - melanom, nierenzellkarzinom, kolorektales karzinom - biotechnologika