Evrópusambandið - litháíska - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - nintedanibas - karcinoma, nesmulkiųjų ląstelių skausmas - antinavikiniai vaistai - vargatef skiriamas kartu su docetakseliu suaugusiems pacientams, sergantiems lokaliai išplitusiu, metastazavusiu ar vietiškai nesmulkiųjų ląstelių plaučių vėžiu (nslpv) gydymo, naviko adenokarcinoma po pirmos eilės chemoterapijos.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - olanzapino pamoato - Šizofrenija - psicholeptikai - suaugusių pacientų, sergančių šizofrenija, priežiūros gydymas yra pakankamai stabilus, kai gydomas geriamasis olanzapinas.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - artritas, reumatas - imunosupresantai - 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). olumianetą galima vartoti kaip monoterapiją arba kartu su metotreksatu. 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.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - abemaciclib - krūties navikai - antinavikiniai vaistai - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - galcanezumab - migrenos sutrikimai - analgesics, galcanezumab - emgality yra nurodyta profilaktika migrena, suaugusiems žmonėms, kurie turi ne mažiau kaip 4 migrena dienas per mėnesį.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - insulinas lispro - cukrinis diabetas - narkotikai, vartojami diabetu - suaugusiems, paaugliams ir vaikams nuo 1 metų ir vyresniems cukrinio diabeto gydymas. suaugusiųjų cukrinio diabeto gydymas.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antinavikiniai vaistai - 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.

Evrópusambandið - litháíska - EMA (European Medicines Agency)

eli lilly nederland b.v. - lasmiditan succinate - migrenos sutrikimai - analgetikai - rayvow is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

Litháen - litháíska - SMCA (Valstybinė vaistų kontrolės tarnyba)

inteli generics nord, uab - ibuprofenas - geriamoji suspensija - 100 mg/5 ml - ibuprofen

Litháen - litháíska - SMCA (Valstybinė vaistų kontrolės tarnyba)

inteli generics nord, uab - imatinibas - plėvele dengtos tabletės - 400 mg; 100 mg - imatinib