Tremfya Unión Europea - español - EMA (European Medicines Agency)

tremfya

janssen-cilag international nv - guselkumab - psoriasis - inmunosupresores - plaque psoriasis tremfya is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritis tremfya, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (dmard) therapy (see section 5.

TREMFYA 100mg/mL SOLUCION INYECTABLE Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

tremfya 100mg/ml solucion inyectable

j&j productos medicos & farmaceuticos del peru s.a. - droguerÍa - guselkumab - solucion inyectable - 100mg/ml - por jeringa precargada 1.00 ml - - guselkumab

TREMFYA® Ecuador - español - Agencia Nacional de Regulación, Control y Vigilancia Sanitaria

tremfya®

janssen biotech inc estados unidos - guselkumab 100 mg/ml - solucion inyectable - cada ml contiene: guselkumab 100 mg

Spevigo Unión Europea - español - EMA (European Medicines Agency)

spevigo

boehringer ingelheim international gmbh - spesolimab - psoriasis - inmunosupresores - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

Bavencio Unión Europea - español - EMA (European Medicines Agency)

bavencio

merck europe b.v. - avelumab - tumores neuroendocrinos - otros agentes antineoplásicos, anticuerpos monoclonales - bavencio está indicado como monoterapia para el tratamiento de pacientes adultos con cáncer metastásico carcinoma de células de merkel (mcc). bavencio en combinación con axitinib está indicado para el tratamiento de primera línea de pacientes adultos con carcinoma avanzado de células renales (rcc). bavencio is indicated as monotherapy for the first‑line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc) who are progression-free following platinum‑based chemotherapy.

Dupixent Unión Europea - español - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agentes para la dermatitis, excluidos los corticosteroides - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.