SINTAFLAT Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

sintaflat

laboratÓrio globo sa - adsorventes e antifiseticos intestinais simples

ANDROSTEN Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

androsten

herbarium laboratorio botanico ltda - tribulus terrestris l. - fitoterapico simples; androgenos simples

CLEXANE Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

clexane

sanofi-aventis farmacÊutica ltda - enoxaparina sÓdica - antitrombotico

ETIRA Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

etira

aché laboratórios farmacêuticos s.a - levetiracetam - anticonvulsivantes

ETIRA Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

etira

aché laboratórios farmacêuticos s.a - levetiracetam - anticonvulsivantes

HEPARINOX Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

heparinox

cristÁlia produtos quÍmicos farmacÊuticos ltda. - enoxaparina sÓdica - antitrombotico

KEPPRA Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

keppra

ucb biopharma ltda. - levetiracetam - anticonvulsivantes

levetiracetam Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

levetiracetam

eurofarma laboratÓrios s.a. - levetiracetam - anticonvulsivantes

VOLIBRIS Brasil - portugués - ANVISA (Agência Nacional de Vigilância Sanitária)

volibris

glaxosmithkline brasil ltda - ambrisentana - anti-hipertensivos

Ultomiris Unión Europea - portugués - EMA (European Medicines Agency)

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.