União Europeia - português - EMA (European Medicines Agency)

meda ab - zaleplon - transtornos de iniciação e manutenção do sono - psicolepticos - a sonata está indicada para o tratamento de pacientes com insônia que têm dificuldade em adormecer. É indicado apenas quando o transtorno é grave, desativando ou sujeitando o indivíduo a uma angústia extrema.

União Europeia - português - EMA (European Medicines Agency)

meda ab - zaleplon - transtornos de iniciação e manutenção do sono - psicolepticos - zerene é indicado para o tratamento de pacientes com insônia que têm dificuldade em adormecer. É indicado apenas quando o transtorno é grave, desativando ou sujeitando o indivíduo a uma angústia extrema.

União Europeia - português - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - pegcetacoplan - hemoglobinúria, paroxística - imunossupressores - aspaveli is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh) who are anaemic after treatment with a c5 inhibitor for at least 3 months.

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

united medical ltda - fumarato de tenofovir desoproxila - antiretroviral

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

united medical ltda - azacitidina - antimetabolicos analogos da pirimidina

União Europeia - português - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - difelikefalin - pruritus - todos os outros produtos terapêuticos - kapruvia is indicated for the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adult patients on haemodialysis (see section 5.

União Europeia - português - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - efmoroctocog alfa - hemofilia a - anti-hemorrágicos - tratamento e profilaxia do sangramento em pacientes com hemofilia a (deficiência congênita de fator viii). elocta pode ser usado para todos os grupos de idade.

União Europeia - português - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinúria, paroxística - imunossupressores seletivos - 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.

União Europeia - português - EMA (European Medicines Agency)

roche registration gmbh - metoxi polietileno glicol-epoetina beta - anemia; kidney failure, chronic - preparações antianêmicas - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.

União Europeia - português - EMA (European Medicines Agency)

novartis europharm limited - vildagliptin, metformin hydrochloride - diabetes mellitus, tipo 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.