Flebogamma DIF (previously Flebogammadif) Evropská unie - čeština - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - normální lidský imunoglobulin - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - imunitní séra a imunoglobuliny, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

Jayempi Evropská unie - čeština - 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.

Blincyto Evropská unie - čeština - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - prekurzorová buněčná lymfoblastická leukémie-lymfom - antineoplastická činidla - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Arti-Cell Forte Evropská unie - čeština - EMA (European Medicines Agency)

arti-cell forte

boehringer ingelheim vetmedica gmbh - chondrogenic vyvolané koní alogenní periferní krve-odvozené mezenchymálních kmenových buněk, - jiné léky na poruchy muskuloskeletálního systému - koně - snížení mírné až středně závažné opakující se kulhání spojené s non-septický zánět kloubů u koní.

ACIFEIN 250MG/200MG/50MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

acifein 250mg/200mg/50mg tableta

herbacos recordati s.r.o., pardubice array - 12 kyselina acetylsalicylovÁ; 1064 paracetamol; 223 kofein - tableta - 250mg/200mg/50mg - paracetamol, kombinace kromĚ psycholeptik

ACYGAL 500MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

acygal 500mg tableta

galmed a.s., ostrava ČeskÁ republika - 12 kyselina acetylsalicylovÁ - tableta - 500mg - kyselina acetylsalicylovÁ

ACYLCOFFIN 450MG/50MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

acylcoffin 450mg/50mg tableta

zentiva a.s., bratislava array - 12 kyselina acetylsalicylovÁ; 223 kofein - tableta - 450mg/50mg - kyselina acetylsalicylovÁ, kombinace kromĚ psycholeptik

ACYLPYRIN 500MG Šumivá tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

acylpyrin 500mg šumivá tableta

herbacos recordati s.r.o., pardubice array - 12 kyselina acetylsalicylovÁ - Šumivá tableta - 500mg - kyselina acetylsalicylovÁ

ACYLPYRIN 500MG Tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

acylpyrin 500mg tableta

herbacos recordati s.r.o., pardubice array - 12 kyselina acetylsalicylovÁ - tableta - 500mg - kyselina acetylsalicylovÁ