ULTOMIRIS 300mg/30ml Koncentrat za rastvor za infuziju Montenegro - kroatia - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

ultomiris 300mg/30ml koncentrat za rastvor za infuziju

druŠtvo za trgovinu na veliko farmaceutskim proizvodima "glosarij" d.o.o.-podgorica - ravulizumab - koncentrat za rastvor za infuziju - 300mg/30ml

Ultomiris Euroopan unioni - kroatia - EMA (European Medicines Agency)

ultomiris

alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektivni imunosupresivi - 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.

Qtrilmet Euroopan unioni - kroatia - EMA (European Medicines Agency)

qtrilmet

astrazeneca ab - метформина hidroklorid, Саксаглиптин, dapagliflozin - dijabetes mellitus, tip 2 - lijekovi koji se koriste u dijabetesu - qtrilmet prikazan u odraslih osoba u dobi od 18 godina i stariji sa dijabetesom tipa 2 za poboljšanje glikemijski kontrole pri metforminom ili bez sulfonilureje (su) i саксаглиптин ili dapagliflozin ne pruža adekvatne kontrole glikemijski . kad već liječenih metforminom i саксаглиптин i dapagliflozin.

HIBIBOS T 0,5 g/100 mL otopina  za kožu Bosnia ja Hertsegovina - kroatia - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

hibibos t 0,5 g/100 ml otopina za kožu

bosnalijek d.d. - hlorheksidin - otopina za kožu - 0,5 g/100 ml - 100 ml otopine za kožu sadrži: 0,5 g klorheksidin diglukonata (u obliku 20 % otopine klorheksidin diglukonata)

ULTOMIRIS 1100mg/11 ml Koncentrat za rastvor za infuziju Montenegro - kroatia - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

ultomiris 1100mg/11 ml koncentrat za rastvor za infuziju

druŠtvo za trgovinu na veliko farmaceutskim proizvodima "glosarij" d.o.o.-podgorica - ravulizumab - koncentrat za rastvor za infuziju - 1100mg/11 ml

ULTOMIRIS 300mg/3ml Koncentrat za rastvor za infuziju Montenegro - kroatia - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

ultomiris 300mg/3ml koncentrat za rastvor za infuziju

druŠtvo za trgovinu na veliko farmaceutskim proizvodima "glosarij" d.o.o.-podgorica - ravulizumab - koncentrat za rastvor za infuziju - 300mg/3ml