Latvija - latviešu - Zāļu valsts aģentūra

actavis nordic a/s, denmark - indometacinum, troxerutinum - gels - 30/20 mg/g

Latvija - latviešu - Zāļu valsts aģentūra

sopharma ad, bulgaria - indometacīns - ziede - 100 mg/g

Latvija - latviešu - Zāļu valsts aģentūra

viatris healthcare limited, ireland - indometacīns - ilgstošās darbības tablete - 75 mg

Latvija - latviešu - Zāļu valsts aģentūra

uab "stada baltics", lithuania - indometacīns - uz ādas lietojams aerosols, šķīdums - 8 mg/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

mylan pharmaceuticals limited - febuxostat - hyperuricemia; arthritis, gouty; gout - antigut preparāti - febuxostat mylan indicēts profilaksi un ārstēšanu pieaugušiem pacientiem veikta ķīmijterapija haematologic malignancies starpproduktu ar augsta riska audzēju līzes sindroms (tls) hyperuricaemia. febuxostat mylan ir indicēts, lai ārstētu hronisku hyperuricaemia apstākļos, kad urate uzklāšanas jau ir noticis (tai skaitā vēsturē, vai klātbūtne, tophus un/vai podagras artrīta). febuxostat mylan ir norādīts pieaugušie.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

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.

Latvija - latviešu - Zāļu valsts aģentūra

b.braun melsungen ag, germany - amikacīns - Šķīdums infūzijām - 5 mg/ml

Latvija - latviešu - Zāļu valsts aģentūra

b.braun melsungen ag, germany - amikacīns - Šķīdums infūzijām - 10 mg/ml

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

eli lilly nederland b.v. - glucagon - cukura diabēts - aizkuņģa dziedzera hormoni, hormoni glycogenolytic - baqsimi ir indicēts, lai ārstētu smagas hipoglikēmijas pieaugušajiem, pusaudžiem un bērniem vecumā no 4 gadiem un vairāk, ar cukura diabēts.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

tetris pharma b.v - glucagon - cukura diabēts - aizkuņģa dziedzera hormoni, hormoni glycogenolytic - ogluo is indicated for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 2 years and over with diabetes mellitus.