Padcev Európska únia - slovenčina - EMA (European Medicines Agency)

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - antineoplastické činidlá - padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 or programmed death ligand 1 inhibitor.

Adcetris Európska únia - slovenčina - EMA (European Medicines Agency)

adcetris

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - antineoplastické činidlá - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris je indikovaný na liečbu dospelých pacientov s relapsed alebo žiaruvzdorné cd30+ hodgkinovým lymfómom (hl):v nadväznosti na asct, orfollowing aspoň dve predchádzajúce terapie pri asct alebo multi-agent chemoterapia nie je možnosť liečby. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Flutiform K-haler 125 mikrogramov/5 mikrogramov Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

flutiform k-haler 125 mikrogramov/5 mikrogramov

mundipharma gesellschaft m.b.h., rakúsko - formoterol a flutikazón - 14 - bronchodilatantia, antiasthmatica

Flutiform K-haler 50 mikrogramov/5 mikrogramov Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

flutiform k-haler 50 mikrogramov/5 mikrogramov

mundipharma gesellschaft m.b.h., rakúsko - formoterol a flutikazón - 14 - bronchodilatantia, antiasthmatica

Flutiform 50 mikrogramov/5 mikrogramov Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

flutiform 50 mikrogramov/5 mikrogramov

mundipharma gesellschaft m.b.h., rakúsko - formoterol a flutikazón - 14 - bronchodilatantia, antiasthmatica

Flutiform 125 mikrogramov/5 mikrogramov Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

flutiform 125 mikrogramov/5 mikrogramov

mundipharma gesellschaft m.b.h., rakúsko - formoterol a flutikazón - 14 - bronchodilatantia, antiasthmatica

Flutiform 250 mikrogramov/10 mikrogramov Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

flutiform 250 mikrogramov/10 mikrogramov

mundipharma gesellschaft m.b.h., rakúsko - formoterol a flutikazón - 14 - bronchodilatantia, antiasthmatica

Yervoy Európska únia - slovenčina - EMA (European Medicines Agency)

yervoy

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastické činidlá - 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 a 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%.

Targin 5/2,5 mg tablety s predĺženým uvoľňovaním Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

targin 5/2,5 mg tablety s predĺženým uvoľňovaním

mundipharma gesellschaft m.b.h., rakúsko - oxykodón a naloxón - 65 - analgetica - anodyna