Unione Europea - italiano - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab, relatlimab - melanoma - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.

Unione Europea - italiano - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - deucravacitinib - psoriasi - immunosoppressori - treatment of moderate-to-severe plaque psoriasis in adults.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - sevelamer - renal dialysis; hyperphosphatemia - tutti gli altri prodotti terapeutici - renagel is indicated for the control of hyperphosphataemia in adult patients receiving  haemodialysis or peritoneal dialysis. renagel should be used within the context of a multiple therapeutic approach, which could include calcium supplements, 1,25 - dihydroxy vitamin d3 or one of its analogues to control the development of renal bone disease.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - agalsidasi beta - malattia di fabry - altro apparato digerente e metabolismo prodotti, - fabrazyme è indicato per la terapia enzimatica sostitutiva a lungo termine in pazienti con diagnosi confermata di malattia di fabry (deficit di α-galattosidasi-a).

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - sevelamer carbonato - hyperphosphatemia; renal dialysis - tutti gli altri prodotti terapeutici - renvela è indicato per il controllo dell'iperfosfatemia in pazienti adulti sottoposti a emodialisi o dialisi peritoneale. renvela è anche indicato per il controllo dell'iperfosfatemia in pazienti adulti con malattia renale cronica non in dialisi con fosforo sierico ≥ 1. 78 mmol/l. renvela deve essere usato nel contesto di un più approccio terapeutico che potrebbe includere integratori di calcio, 1,25-diidrossi-vitamina d3 o uno dei suoi analoghi, per controllare lo sviluppo della malattia ossea renale.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - sevelamer carbonato - hyperphosphatemia; renal dialysis - tutti gli altri prodotti terapeutici - sevelamer carbonato di winthrop è indicato per il controllo dell'iperfosfatemia in pazienti adulti sottoposti ad emodialisi o a dialisi peritoneale. sevelamer carbonato di winthrop è anche indicato per il controllo dell'iperfosfatemia in pazienti adulti con malattia renale cronica non in dialisi con fosforo sierico > 1. 78 mmol / l. sevelamer carbonato di winthrop deve essere usato nel contesto di un più approccio terapeutico che potrebbe includere integratori di calcio, 1,25-diidrossi-vitamina d3 o uno dei suoi analoghi, per controllare lo sviluppo della malattia ossea renale.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - tireotropina alfa - neoplasie della tiroide - dell'ipofisi anteriore del lobo ormoni e farmaceutici, l'ipofisi e l'ipotalamo gli ormoni e farmaceutici - thyrogen is indicated for use with serum thyroglobulin (tg) testing with or without radioiodine imaging for the detection of thyroid remnants and well-differentiated thyroid cancer in post thyroidectomy patients maintained on hormone suppression therapy (thst). low risk patients with well-differentiated thyroid carcinoma who have undetectable serum tg levels on thst and no rh (recombinant human) tsh-stimulated increase of tg levels may be followed-up by assaying rh tsh-stimulated tg levels. thyrogen is indicated for pre-therapeutic stimulation in combination with a range of 30 mci (1. 1 gbq) to 100 mci (3. 7 gbq) radioiodine for ablation of thyroid tissue remnants in patients who have undergone a near-total or total thyroidectomy for well-differentiated thyroid cancer and who do not have evidence of distant metastatic thyroid cancer (see section 4.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabete mellito - farmaci usati nel diabete - diabete mellito dove è richiesto il trattamento con insulina. insuman rapid è anche adatto per il trattamento del coma iperglicemico e chetoacidosi, nonché per raggiungere pre-, intra - e stabilizzazione postoperatoria in pazienti con diabete mellito.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agenti per dermatiti, esclusi i corticosteroidi - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glicogen storage disease type ii - altro apparato digerente e metabolismo prodotti, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).