tacrolimus stada 1 mg kapsułka o przedłużonym uwalnianiu, twarda
stada arzneimittel ag - tacrolimusum monohydricum - kapsułka o przedłużonym uwalnianiu, twarda - 1 mg
dabigatran eteksylan stada 150 mg kapsułki twarde
stada arzneimittel ag - dabigatranu eteksylan w postaci mezylanu - kapsułki twarde - 150 mg
dabigatran eteksylan stada 110 mg kapsułki twarde
stada arzneimittel ag - dabigatranu eteksylan w postaci mezylanu - kapsułki twarde - 110 mg
dabigatran eteksylan stada 75 mg kapsułki twarde
stada arzneimittel ag - dabigatranu eteksylan w postaci mezylanu - kapsułki twarde - 75 mg
microgynon 21 30 mcg + 150 mcg tabletki powlekane
bayer ag - ethinylestradiolum + levonorgestrelum - tabletki powlekane - 30 mcg + 150 mcg
logest 0,075 mg + 0,02 mg tabletki powlekane
bayer ag - gestodenum + ethinylestradiolum - tabletki powlekane - 0,075 mg + 0,02 mg
climara-50 50 mcg/24 h (3,8 mg) system transdermalny
bayer ag - estradiolum - system transdermalny - 50 mcg/24 h (3,8 mg)
imatinib actavis
actavis group ptc ehf - imatinib - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma - protein kinase inhibitors, antineoplastic agents - imatinib actavis is indicated for the treatment of: , paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment;, paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis;, adult patients with ph+ cml in blast crisis;, adult patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy;, adult patients with relapsed or refractory ph+ all as monotherapy;, adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements;, adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfr rearrangement;, the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. efekt imatinib na wynik przeszczepienia szpiku kostnego nie jest określona. imatinib actavis is indicated for: , in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic dfsp. doświadczenie z imatinibom u pacjentów z mds/jest msy, związanych z pdgfr genów permutacji-bardzo ograniczony. brak kontrolowanych badań wykazują kliniczną korzyść lub zwiększone tempo dla tych chorób.
ultravist 300 623,4 mg/ml roztwór do wstrzykiwań
bayer ag - iopromidum - roztwór do wstrzykiwań - 623,4 mg/ml
ultravist 370 768,86 mg/ml roztwór do wstrzykiwań
bayer ag - iopromidum - roztwór do wstrzykiwań - 768,86 mg/ml