Europäische Union - Deutsch - EMA (European Medicines Agency)

ferring pharmaceuticals a/s - degarelix - prostata-neoplasmen - endokrine therapie - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

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

recordati industria chimica e farmaceutica s.p.a. (3259649) - leuprorelinmonoacetat - pulver und lösungsmittel zur herstellung einer injektionslösung - teil 1 - pulver zur herstellung einer injektionslösung; leuprorelinmonoacetat (34837) 59,2 milligramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

accord healthcare s.l.u. - degarelix acetate - prostata-neoplasmen - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

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

recordati industria chimica e farmaceutica s.p.a. (3259649) - leuprorelinmonoacetat - pulver und lösungsmittel zur herstellung einer injektionslösung - teil 1 - pulver zur herstellung einer injektionssuspension; leuprorelinmonoacetat (34837) 29,2 milligramm

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

hikma farmaceutica (portugal), s.a. (8007071) - docetaxel - konzentrat zur herstellung einer infusionslösung - teil 1 - konzentrat zur herstellung einer infusionslösung; docetaxel (26819) 160 milligramm

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

hikma farmaceutica (portugal), s.a. (8007071) - docetaxel - konzentrat zur herstellung einer infusionslösung - teil 1 - konzentrat zur herstellung einer infusionslösung; docetaxel (26819) 80 milligramm

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

hikma farmaceutica (portugal), s.a. (8007071) - docetaxel - konzentrat zur herstellung einer infusionslösung - teil 1 - konzentrat zur herstellung einer infusionslösung; docetaxel (26819) 20 milligramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

laboratorios hipra, s.a. - eimeria acervulina, dehnungs-003, eimeria maxima, stamm 013, eimeria mitis -, dehnungs-006, eimeria praecox -, dehnungs-007, eimeria tenella -, dehnungs-004 - live parasitäre impfstoffen, immunologischen arzneimitteln für aves - hähnchen - für die aktive immunisierung von küken, 1 tag alt zu verringern intestinale läsionen und oozysten ausgabe im zusammenhang mit kokzidiose verursacht durch eimeria acervulina, eimeria maxima, eimeria mitis, eimeria praecox und eimeria tenella und zur verringerung der klinischen symptome (durchfall) im zusammenhang mit eimeria acervulina, eimeria maxima und eimeria tenella.

Europäische Union - Deutsch - EMA (European Medicines Agency)

samsung bioepis nl b.v. - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastische mittel - aybintio in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. aybintio in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. weitere informationen zum status des humanen epidermalen wachstumsfaktor-rezeptors 2 (her2) finden sie in abschnitt 5. 1 of the smpc. aybintio in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracyclinecontaining regimens in the adjuvant setting within the last 12 months should be excluded from treatment with aybintio in combination with capecitabine. weitere informationen zum her2-status finden sie in abschnitt 5. 1 of the smpc. aybintio, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. aybintio, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. 1 of the smpc). aybintio in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. aybintio, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. 1 of the smpc). aybintio, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents. aybintio, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. 1 of the smpc). aybintio, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5. 1 of the smpc).

Europäische Union - Deutsch - EMA (European Medicines Agency)

centus biotherapeutics europe limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell - antineoplastische mittel - bevacizumab in kombination mit fluoropyrimidin-basierten chemotherapie ist für die behandlung von erwachsenen patienten mit metastasiertem kolon- oder rektumkarzinom indiziert. bevacizumab in kombination mit paclitaxel ist angezeigt für die first-line-behandlung von erwachsenen patienten mit metastasiertem brustkrebs. weitere informationen zum status des humanen epidermalen wachstumsfaktor-rezeptors 2 (her2) finden sie in abschnitt 5. bevacizumab in kombination mit capecitabin angezeigt zur first-line-behandlung von erwachsenen patienten mit metastasiertem brustkrebs, bei denen eine behandlung mit anderen chemotherapie-optionen auf der basis von taxanen oder anthracyclinen, nicht angemessen ist. patients who have received taxane and anthracycline- containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with equidacent in combination with capecitabine. weitere informationen zum her2-status finden sie in abschnitt 5. bevacizumab, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. bevacizumab, in kombination mit erlotinib, ist angezeigt für die first-line-behandlung von erwachsenen patienten mit nicht operierbarem, fortgeschrittenem, metastasiertem oder rezidivierendem nicht-squamösen nicht-kleinzelligem lungenkrebs mit epidermalen wachstumsfaktor-rezeptor (egfr-aktivierenden mutationen. bevacizumab in combination with interferon alfa-2a is indicated for first-line treatment of adult patients with advanced and/or metastatic renal cell cancer. bevacizumab, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iiib, iiic and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. bevacizumab, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor-targeted agents. bevacizumab in kombination mit paclitaxel und cisplatin oder, alternativ, paclitaxel und topotecan bei patienten, die nicht erhalten platinum-therapie, ist indiziert für die behandlung von erwachsenen patienten mit persistierendem, rezidivierendem oder metastasierendem karzinom des gebärmutterhalses.