vyvgart
argenx - efgartigimod alfa - myasthenia gravis - imunossupressores - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.
ultomiris
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.
bezafibrato
ems s/a - bezafibrato - antilipemicos
bezafibrato
fundaÇÃo para o remÉdio popular - furp - bezafibrato - antilipemicos
finadyne transdermal 50 mg/ml solução para unção contínua para bovinos
msd animal health, lda. - flunixina 50.0 mg - solução para unção contínua - flunixina - bovinos
soliris
alexion europe sas - eculizumab - hemoglobinúria, paroxística - imunossupressores - soliris é indicado em adultos e crianças para o tratamento de:hemoglobinúria paroxística noturna (hpn). evidência de benefício clínico é demonstrado em pacientes com hemólise com sintoma clínico(s) indicativo de alta atividade de doença, independentemente de transfusão de história (consulte a secção 5. atípico hemolítica síndrome urêmico (ahus). soliris é indicado em adultos para o tratamento de:refractários generalizada miastenia gravis (gmg), em pacientes que são anti-receptor de acetilcolina (achr, em inglês) anticorpo positivo (consulte a secção 5. neuromielite óptica transtorno do espectro (nmosd) em pacientes que são anti-aquaporina-4 (aqp4) anticorpo positivo com um reincidente curso da doença.
mg-bac - vacina contra mycoplasma gallisepticum
zoetis indÚstria de produtos veterinÁrios ltda - vac. micoplasmose; - vacinas, corantes e diluentes (biolÓgicos)
merional hg
ucb biopharma ltda. - menotropina - hormonio gonadotrofico
keppra
ucb biopharma ltda. - levetiracetam - anticonvulsivantes
candesartan + hidroclorotiazida ritisca 16 mg + 12.5 mg comprimido
generis farmacêutica, s.a. - candesartan + hidroclorotiazida - comprimido - 16 mg + 12.5 mg - hidroclorotiazida 12.5 mg ; candesartan cilexetil 16 mg - candesartan and diuretics - genérico - duração do tratamento: longa duração