Jakavi Ευρωπαϊκή Ένωση - Πορτογαλικά - EMA (European Medicines Agency)

jakavi

novartis europharm limited - ruxolitinib (como fosfato) - myeloproliferative disorders; polycythemia vera; graft vs host disease - agentes antineoplásicos - myelofibrosis (mf)jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. polycythaemia vera (pv)jakavi é indicado para o tratamento de pacientes adultos com polycythaemia vera que são resistentes ou intolerantes hydroxyurea. graft versus host disease (gvhd)jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.

Opzelura Ευρωπαϊκή Ένωση - Πορτογαλικά - EMA (European Medicines Agency)

opzelura

incyte biosciences distribution b.v. - ruxolitinib phosphate - vitiligo - outras preparações dermatológicas - opzelura is indicated for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age.

Inrebic Ευρωπαϊκή Ένωση - Πορτογαλικά - EMA (European Medicines Agency)

inrebic

bristol myers squibb pharma eeig - fedratinib dihydrochloride monohydrate - myeloproliferative disorders; primary myelofibrosis - agentes antineoplásicos - inrebic is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis who are janus associated kinase (jak) inhibitor naïve or have been treated with ruxolitinib.

DUO-DECADRON Βραζιλία - Πορτογαλικά - ANVISA (Agência Nacional de Vigilância Sanitária)

duo-decadron

aché laboratórios farmacêuticos s.a - acetato de dexametasona, fosfato dissÓdico de dexametasona - glicocorticoides sistemicos

SPORANOX Βραζιλία - Πορτογαλικά - ANVISA (Agência Nacional de Vigilância Sanitária)

sporanox

janssen-cilag farmacÊutica ltda - itraconazol - antimicoticos sistemicos

Yescarta Ευρωπαϊκή Ένωση - Πορτογαλικά - EMA (European Medicines Agency)

yescarta

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - agentes antineoplásicos - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.