vixargio 10 mg tabletki powlekane
viatris ltd - rivaroxabanum - tabletki powlekane - 10 mg
vixargio 2,5 mg tabletki powlekane
viatris ltd - rivaroxabanum - tabletki powlekane - 2,5 mg
vixargio 20 mg tabletki powlekane
viatris ltd - rivaroxabanum - tabletki powlekane - 20 mg
sunitinib zentiva 50 mg kapsułki twarde
zentiva, k.s. - sunitinibum - kapsułki twarde - 50 mg
sunitinib zentiva 12,5 mg kapsułki twarde
zentiva, k.s. - sunitinibum - kapsułki twarde - 12,5 mg
sunitinib zentiva 37,5 mg kapsułki twarde
zentiva, k.s. - sunitinibum - kapsułki twarde - 37,5 mg
sunitinib zentiva 25 mg kapsułki twarde
zentiva, k.s. - sunitinibum - kapsułki twarde - 25 mg
ultomiris
alexion europe sas - ravulizumab - hemoglobinuria, paroksysmal - selektywne leki immunosupresyjne - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.
pemetrexed actavis 500 mg proszek do sporządzania koncentratu roztworu do infuzji
actavis group ptc ehf. - pemetrexedum dinatricum hemipentahydricum - proszek do sporządzania koncentratu roztworu do infuzji - 500 mg
pemetrexed actavis 100 mg proszek do sporządzania koncentratu roztworu do infuzji
actavis group ptc ehf. - pemetrexedum dinatricum hemipentahydricum - proszek do sporządzania koncentratu roztworu do infuzji - 100 mg