Ibrance Eiropas Savienība - latviešu - EMA (European Medicines Agency)

ibrance

pfizer europe ma eeig  - palbociklibs - krūts audzējs - antineoplastiski līdzekļi - ibrance ir indicēts, lai ārstētu hormonu receptoru (ap) pozitīvs, cilvēka epidermas augšanas faktora receptora 2 (her2) negatīvs vietas papildu vai metastātisku krūts vēzi:kombinācijā ar aromatāzes inhibitoru;kopā ar fulvestrants sievietes, kas ir saņemti pirms endokrīnās terapijas. pre - vai perimenopausal sievietēm, endokrīnās terapijas būtu jāapvieno ar luteinizējošais hormona atbrīvojošo hormonu (lhrh) agonistu.

Cyltezo Eiropas Savienība - latviešu - EMA (European Medicines Agency)

cyltezo

boehringer ingelheim international gmbh - adalimumab - hidradenitis suppurativa; arthritis, psoriatic; psoriasis; crohn disease; arthritis, juvenile rheumatoid; uveitis; arthritis, rheumatoid; colitis, ulcerative; spondylitis, ankylosing - imūnsupresanti - lūdzu, skatiet 4. sadaļu. produkta raksturojuma kopsavilkums 1 produkta informācijas dokumentā.

Samsca Eiropas Savienība - latviešu - EMA (European Medicines Agency)

samsca

otsuka pharmaceutical netherlands b.v. - tolvaptāns - nepiemērots adh sindroms - diurētiskie līdzekļi, - pieaugušiem pacientiem ar hiponatriēmiju, kas saistīta ar nepiemērotu antidiuretiskās hormona sekrēcijas sindromu (siadh).

Viekirax Eiropas Savienība - latviešu - EMA (European Medicines Agency)

viekirax

abbvie deutschland gmbh co. kg - ombitasvir, paritaprevir, ritonavir - c hepatīts, hronisks - pretvīrusu līdzekļi sistēmiskai lietošanai - viekirax ir minēta kopā ar citām zālēm, ārstēšanai hronisku c hepatītu (chc) pieaugušajiem. hepatīta c vīrusa (hcv) genotipa specifiska aktivitāte.

Ebetrex 20 mg/ml šķīdums injekcijām pilnšļircēs Latvija - latviešu - Zāļu valsts aģentūra

ebetrex 20 mg/ml šķīdums injekcijām pilnšļircēs

sandoz d.d., slovenia - metotreksāts - Šķīdums injekcijām pilnšļircē - 20 mg/ml

Fercelan 202,8 mg/0,8 mg/100 mg cietās kapsulas Latvija - latviešu - Zāļu valsts aģentūra

fercelan 202,8 mg/0,8 mg/100 mg cietās kapsulas

g.l. pharma gmbh, austria - ferrosi fumaras, acid-folicum, skābes ascorbicum - kapsula, cietā - 202,8 mg/0,8 mg/100 mg

Nubeqa Eiropas Savienība - latviešu - EMA (European Medicines Agency)

nubeqa

bayer ag - darolutamide - prostatas audzējiem, kastrācija-izturīgs - endokrīnā terapija - nubeqa is indicated for the treatment of adult men with- non metastatic castration resistant prostate cancer (nmcrpc) who are at high risk of developing metastatic disease (see section 5. - metastatic hormone sensitive prostate cancer (mhspc) in combination with docetaxel and androgen deprivation therapy (see section 5.

Exparel liposomal Eiropas Savienība - latviešu - EMA (European Medicines Agency)

exparel liposomal

pacira ireland limited - bupivakaīns - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

Jayempi Eiropas Savienība - latviešu - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azatioprīns - transplanta noraidīšana - imūnsupresanti - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Tifay 14 mg apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

tifay 14 mg apvalkotās tabletes

stada arzneimittel ag, germany - teriflunomīds - apvalkotā tablete - 14 mg