Cabometyx 20 mg Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

cabometyx 20 mg filmtabletten

ipsen pharma schweiz gmbh - cabozantinibum - filmtabletten - cabozantinibum 20 mg ut cabozantinibi l-malas 25.34 mg, cellulosum microcristallinum, lactosum 15.54 mg, hydroxypropylcellulosum, carmellosum natricum conexum corresp. natrium 0.9 mg, silica colloidalis anhydrica, magnesii stearas, Überzug: hypromellosum, triacetinum, e 171, e 172 (flavum), pro compresso obducto. - nierenzellkarzinom, leberzellkarzinom, schilddrüsenkarzinom - synthetika

Cabometyx 40 mg Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

cabometyx 40 mg filmtabletten

ipsen pharma schweiz gmbh - cabozantinibum - filmtabletten - cabozantinibum 40 mg ut cabozantinibi l-malas 50.69 mg, cellulosum microcristallinum, lactosum 31.07 mg, hydroxypropylcellulosum, carmellosum natricum conexum corresp. natrium 1.8 mg, silica colloidalis anhydrica, magnesii stearas, Überzug: hypromellosum, triacetinum, e 171, e 172 (flavum), pro compresso obducto. - nierenzellkarzinom, leberzellkarzinom, schilddrüsenkarzinom - synthetika

Cabometyx 60 mg Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

cabometyx 60 mg filmtabletten

ipsen pharma schweiz gmbh - cabozantinibum, natrium - filmtabletten - cabozantinibum 60 mg ut cabozantinibi l-malas 76.03 mg, cellulosum microcristallinum, lactosum 46.61 mg, hydroxypropylcellulosum, carmellosum natricum conexum corresp. natrium 2.7 mg, silica colloidalis anhydrica, magnesii stearas, Überzug: hypromellosum, triacetinum, e 171, e 172 (flavum), pro compresso obducto. - nierenzellkarzinom, leberzellkarzinom, schilddrüsenkarzinom - synthetika

Cabometyx Europäische Union - Deutsch - 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.

Cometriq Europäische Union - Deutsch - EMA (European Medicines Agency)

cometriq

ipsen pharma - cabozantinib - schilddrüsenneoplasmen - antineoplastische mittel - behandlung von erwachsenen patienten mit progressivem, nicht resezierbarem lokal fortgeschrittenem oder metastasiertem medullärem schilddrüsenkarzinom.

Tabrecta 150 mg Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

tabrecta 150 mg filmtabletten

novartis pharma schweiz ag - capmatinibum - filmtabletten - capmatinibum 150 mg ut capmatinibi hydrochloridum monohydricum, cellulosum microcristallinum, mannitolum, crospovidonum, povidonum k 30, magnesii stearas, silica colloidalis anhydrica, natrii laurilsulfas corresp. natrium 0.12 mg, Überzug: hypromellosum, e 171, macrogolum 4000, talcum, e 172 (flavum), e 172 (rubrum), e 172 (nigrum), pro compresso obducto. - nicht-kleinzelliges lungenkarzinom - synthetika

Tabrecta 200 mg Filmtabletten Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

tabrecta 200 mg filmtabletten

novartis pharma schweiz ag - capmatinibum - filmtabletten - capmatinibum 200 mg ut capmatinibi hydrochloridum monohydricum, cellulosum microcristallinum, mannitolum, crospovidonum, povidonum k 30, magnesii stearas, silica colloidalis anhydrica, natrii laurilsulfas corresp. natrium 0.16 mg, Überzug: hypromellosum, e 171, macrogolum 4000, talcum, e 172 (flavum), pro compresso obducto. - nicht-kleinzelliges lungenkarzinom - synthetika

Opdivo Europäische Union - Deutsch - EMA (European Medicines Agency)

opdivo

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - antineoplastische mittel - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. 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. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab 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. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab 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. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab 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%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy 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%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.

Itraconazol AbZ 100 mg Hartkapseln Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

itraconazol abz 100 mg hartkapseln

abz-pharma gmbh - geschäftsanschrift - (4238075) - itraconazol - hartkapsel - teil 1 - hartkapsel; itraconazol (23401) 100 milligramm

Itraconazol-ratiopharm 100 mg Hartkapseln Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

itraconazol-ratiopharm 100 mg hartkapseln

ratiopharm gmbh (3087881) - itraconazol - hartkapsel - teil 1 - hartkapsel; itraconazol (23401) 100 milligramm