Lextemy 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

lextemy

mylan ire healthcare limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastična sredstva - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.

Novtirox 150 mikrogramov tablete 斯洛文尼亚 - 斯洛文尼亚文 - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

novtirox 150 mikrogramov tablete

aspen pharma trading limited - natrijev levotiroksinat - tableta - natrijev levotiroksinat 150 mg / 1 tableta - natrijev levotiroksinat

Afinitor 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

afinitor

novartis europharm limited - everolimus - carcinoma, renal cell; breast neoplasms; pancreatic neoplasms - antineoplastična sredstva - hormon-receptor-pozitivno napredno prsi cancerafinitor je primerna za zdravljenje hormon-receptor-pozitiven, her2/neu-negativne napredno raka na dojki, v kombinaciji z exemestane, v post-menopavzi, brez simptomatsko visceralne bolezni po ponovitev ali napredovanje po nesteroidna zaviralec aromataze. neuroendocrine tumorji trebušne slinavke originafinitor je primerna za zdravljenje unresectable ali metastatskim, dobro ali zmerno diferenciran neuroendocrine tumorji trebušne slinavke izvora pri odraslih z progresivna bolezen,. neuroendocrine tumorji iz prebavil ali pljuč originafinitor je primerna za zdravljenje unresectable ali metastatskim, dobro diferencirana (razred 1 ali razred 2) ne-funkcionalne neuroendocrine tumorji iz prebavil ali pljuč izvora pri odraslih z progresivna bolezen,. ledvične celice carcinomaafinitor je indiciran za zdravljenje bolnikov z napredovalim ledvičnim-cell carcinoma, katerih bolezen je napredovala na ali po zdravljenju z vegf-usmerjena terapija.

Inlyta 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

inlyta

pfizer europe ma eeig  - axitinib - karcinom, ledvična celica - proteinska kinaza inhibitorji - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

Invirase 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

invirase

roche registration gmbh - sakvinavir - okužbe z virusom hiv - antivirusi za sistemsko uporabo - zdravilo invirase je indicirano za zdravljenje odraslih bolnikov s hiv-1. zdravilo invirase se lahko daje le v kombinaciji z ritonavirjem in drugimi protiretrovirusnimi zdravili.

Ketoconazole HRA 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

ketoconazole hra

hra pharma rare diseases - ketokonazol - cushingov sindrom - antimikotiki za sistemsko uporabo - ketokonazol hra je indiciran za zdravljenje endogenega cushingovega sindroma pri odraslih in mladostnikih, starejših od 12 let.

Kisplyx 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

kisplyx

eisai gmbh - lenvatinib mesilat - karcinom, ledvična celica - antineoplastična sredstva - kisplyx is indicated for the treatment of adults with advanced renal cell carcinoma (rcc):in combination with pembrolizumab, as first-line treatment (see section 5. in combination with everolimus, following one prior vascular endothelial growth factor (vegf)-targeted therapy.

Yervoy 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

yervoy

bristol-myers squibb pharma eeig - ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastična sredstva - 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 in 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%.

Voriconazole Accord 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

voriconazole accord

accord healthcare s.l.u. - vorikonazol - aspergillosis; candidiasis; mycoses - antimycotics za sistemsko uporabo, triazol derivati - voriconazole je v širokem spektru, triazol protiglivično sredstvo, ter je označena pri odraslih in otrocih, starih dve leti ali več, kot sledi:zdravljenje invazivne aspergillosis;zdravljenje candidaemia v ne-neutropenic bolnikov;zdravljenje fluconazole-odporne resno invazivne candida okužbe (vključno c. krusei);zdravljenje hude glivične okužbe, ki jih povzročajo scedosporium spp. in oxysporum spp. voriconazole soglasju mora biti urejen, predvsem pri bolnikih z napredujočo, morda celo smrtno nevarne okužbe.

Voriconazole Hikma (previously Voriconazole Hospira) 欧盟 - 斯洛文尼亚文 - EMA (European Medicines Agency)

voriconazole hikma (previously voriconazole hospira)

hikma farmaceutica (portugal) s.a. - vorikonazol - bacterial infections and mycoses; aspergillosis; candidiasis - antimikotiki za sistemsko uporabo - voriconazole je širok spekter, triazol protiglivično sredstvo, ter je označena pri odraslih in otrocih, starih 2 leti in več, kot sledi:zdravljenje invazivne aspergillosis;zdravljenje candidaemia v ne-neutropenic bolnikov;zdravljenje fluconazole-odporne resno invazivne candida okužbe (vključno c. krusei);zdravljenje hude glivične okužbe, ki jih povzročajo scedosporium spp. in oxysporum spp. voriconazole je treba preskusiti, predvsem pri bolnikih z napredujočo, morda celo smrtno nevarne okužbe. profilaksa invazivnih glivičnih okužb v visoko tveganje allogeneic hematopoietic matičnih celic za presajanje (hsct)prejemniki.