Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

venipharm, francúzsko - enoxaparín - 16 - anticoagulantia (fibrinolytica, antifibrinol.)

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

venipharm, francúzsko - enoxaparín - 16 - anticoagulantia (fibrinolytica, antifibrinol.)

Európska únia - slovenčina - EMA (European Medicines Agency)

biosimilar collaborations ireland limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastické činidlá - abevmy in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. abevmy in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. Ďalšie informácie o stave receptora ľudského epidermálneho rastového faktora 2 (her2) nájdete v časti 5. abevmy 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 anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with abevmy in combination with capecitabine. Ďalšie informácie o stave her2 nájdete v časti 5. abevmy, 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. abevmy, 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. abevmy in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. abevmy, 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. abevmy, 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. abevmy in combination with paclitaxel, 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. abevmy, 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.

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

zentiva a.s., slovensko - sildenafil - 83 - vasodilatantia

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

zentiva a.s., slovensko - sildenafil - 83 - vasodilatantia

Európska únia - slovenčina - EMA (European Medicines Agency)

clinuvel europe limited - afamelanotide - protoporphyria, erythropoietic - zmäkčovadlá a ochranné prostriedky - prevencia fototoxicita u dospelých pacientov s erytropoetická protoporphyria (eĽs).

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

adamed czech republic s.r.o., Česká republika - klaritromycín - 15 - antibiotica (proti mikrob. a vÍrusovÝm infekciam)

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

as olainfarm, lotyšsko - nitrofurantoín - 42 - chemotherapeutica (vratane tuberkulostatik)

Európska únia - slovenčina - EMA (European Medicines Agency)

piramal critical care b.v. - miglustat - gaucherova choroba - iné alimentárny trakt a metabolizmus výrobky, - yargesa je indikovaný na ústnej liečbe dospelých pacientov s mierne až stredne typ 1 gaucher ochorenia. yargesa môže byť použitý iba v liečbe pacientov, pre ktorých je enzým substitučná terapia je nevhodné. yargesa je indikovaný na liečbu progresívne neurologické prejavy u dospelých pacientov a pediatrických pacientov s niemann-pick typ c ochorenia.

Európska únia - slovenčina - EMA (European Medicines Agency)

gen.orph - miglustat - gaucherova choroba - iné alimentárny trakt a metabolizmus výrobky, - miglustat gen. orph je indikovaný na perorálnu liečbu dospelých pacientov s miernym až stredne ťažkým gaucherovým ochorením typu 1. miglustat gen. orph môže byť použitý iba v liečbe pacientov, pre ktorých je enzým substitučná terapia je nevhodné. miglustat gen. orph je indikovaný na liečbu progresívne neurologické prejavy u dospelých pacientov a pediatrických pacientov s niemann-pick typ c ochorenia.