Neofordex Europäische Union - Tschechisch - EMA (European Medicines Agency)

neofordex

theravia - dexamethason - mnohočetný myelom - kortikosteroidy pro systémové použití - léčba mnohočetného myelomu.

Shingrix Europäische Union - Tschechisch - EMA (European Medicines Agency)

shingrix

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - herpes zoster - vakcíny - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz. použití shingrix by měla být v souladu s oficiálními doporučeními.

Jayempi Europäische Union - Tschechisch - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - odmítnutí štěpu - imunosupresiva - 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.

Vectormune FP ILT Europäische Union - Tschechisch - EMA (European Medicines Agency)

vectormune fp ilt

ceva-phylaxia co. ltd. - recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus, live - kuře - for active immunisation of chickens from 8 weeks of age in order to reduce the skin lesions due to fowlpox and to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis.

Tecovirimat SIGA Europäische Union - Tschechisch - EMA (European Medicines Agency)

tecovirimat siga

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - antivirotika pro systémové použití - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 a 5. tecovirimat siga should be used in accordance with official recommendations.

AMINOPLASMAL B.BRAUN 10% Infuzní roztok Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

aminoplasmal b.braun 10% infuzní roztok

b. braun melsungen ag, melsungen array - 790 isoleucin; 829 leucin; 4566 lysin-acetÁt; 13214 monohydrÁt lysinu; 2445 methionin; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 27 alanin; 55 glycin; 103 kyselina asparagovÁ; 665 kyselina glutamovÁ; 4147 prolin; 4717 serin; 1507 tyrosin - infuzní roztok - aminokyseliny

AMINOPLASMAL B.BRAUN 5% E Infuzní roztok Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

aminoplasmal b.braun 5% e infuzní roztok

b. braun melsungen ag, melsungen array - 790 isoleucin; 829 leucin; 851 lysin-hydrochlorid; 2445 methionin; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 27 alanin; 55 glycin; 103 kyselina asparagovÁ; 665 kyselina glutamovÁ; 4147 prolin; 4717 serin; 1507 tyrosin; 1306 trihydrÁt natrium-acetÁtu; 2458 hydroxid sodnÝ; 1170 kalium-acetÁt; 1322 chlorid sodnÝ; 856 hexahydrÁt chloridu hoŘeČnatÉho; 1341 dodekahydrÁt hydrogenfosforeČnanu sodnÉho - infuzní roztok - roztoky pro parenterÁlnÍ vÝŽivu, kombinace

AMINOPLASMAL HEPA 10% Infuzní roztok Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

aminoplasmal hepa 10% infuzní roztok

b. braun melsungen ag, melsungen array - 790 isoleucin; 829 leucin; 4566 lysin-acetÁt; 2445 methionin; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 55 glycin; 27 alanin; 4147 prolin; 103 kyselina asparagovÁ; 1589 monohydrÁt asparaginu; 1551 acetylcystein; 665 kyselina glutamovÁ; 4734 ornithin-hydrochlorid; 4717 serin; 4564 acetyltyrosin - infuzní roztok - aminokyseliny

AMINOPLASMAL 15% Infuzní roztok Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

aminoplasmal 15% infuzní roztok

b. braun melsungen ag, melsungen array - 790 isoleucin; 829 leucin; 13214 monohydrÁt lysinu; 2445 methionin; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 27 alanin; 55 glycin; 103 kyselina asparagovÁ; 665 kyselina glutamovÁ; 4147 prolin; 4717 serin; 1507 tyrosin; 1551 acetylcystein - infuzní roztok - aminokyseliny

AMINOSTERIL N HEPA 8% Infuzní roztok Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

aminosteril n hepa 8% infuzní roztok

fresenius kabi ab, uppsala array - 790 isoleucin; 829 leucin; 4566 lysin-acetÁt; 2445 methionin; 1551 acetylcystein; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 55 glycin; 27 alanin; 4147 prolin; 4717 serin - infuzní roztok - aminokyseliny