Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - duloxetina cloridrato - incontinenza urinaria, stress - psychoanaleptics, - yentreve è indicato per le donne per il trattamento dell'incontinenza urinaria da moderata a grave (sui).

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - dulaglutide - diabete mellito, tipo 2 - drugs used in diabetes, blood glucose lowering drugs, excl. insulins - trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. per i risultati dello studio rispetto alle combinazioni di effetti sul controllo glicemico e di eventi cardiovascolari, e le popolazioni studiate, vedere sezioni 4. 4, 4. 5 e 5.

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - artrite, reumatoide - immunosoppressori - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant può essere usato in monoterapia o in combinazione con metotrexato. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - raloxifene cloridrato - osteoporosi, postmenopausa - ormoni sessuali e modulatori del sistema genitale, - optruma è indicato per il trattamento e la prevenzione dell'osteoporosi nelle donne in post-menopausa. È stata dimostrata una significativa riduzione dell'incidenza di fratture vertebrali, ma non di quelle dell'anca. nel determinare la scelta di optruma o altre terapie, inclusa quella con estrogeni, per una donna postmenopausale individuo, considerazione dovrebbe essere data sintomi della menopausa, gli effetti sui uterini e mammari tessuti e i rischi cardiovascolari e benefici (vedi sezione 5.

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - agenti antineoplastici - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - tirzepatide - diabete mellito, tipo 2 - farmaci usati nel diabete - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 e 5.

Unione Europea - italiano - EMA (European Medicines Agency)

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Unione Europea - italiano - EMA (European Medicines Agency)

eli lilly nederland b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - omeostasi del calcio - trattamento dell'osteoporosi nelle donne in postmenopausa e negli uomini a maggior rischio di frattura. nelle donne in postmenopausa è stata dimostrata una significativa riduzione dell'incidenza di fratture vertebrali e non vertebrali ma non di fratture dell'anca. trattamento dell'osteoporosi associata sostenuto sistemica terapia con glucocorticoidi nelle donne e negli uomini ad aumentato rischio di frattura.

Italia - italiano - Ministero della Salute

eli lilly and company pharmaceutical delivery systems - siringhe per iniettore

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

eli lilly italia s.p.a. - pergolide - pergolide