Den europeiske union - ungarsk - EMA (European Medicines Agency)

pfizer limited - szunitinibbel - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - daganatellenes szerek - gastrointestinal stromal tumour (gist)sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. experience with sutent as first-line treatment is limited (see section 5.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

biogen netherlands b.v. - dimetil-fumarát - szklerózis multiplex - immunszuppresszánsok - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Den europeiske union - ungarsk - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - lumacaftor, ivacaftor - cisztás fibrózis - egyéb légzőszervi termékek - orkambi tabletta javallott a cisztás fibrózis (cf) a betegek éves 6 éves vagy idősebb, akik homozigóta a f508del mutáció a cftr gén. orkambi granules are indicated for the treatment of cystic fibrosis (cf) in children aged 1 year and older who are homozygous for the f508del mutation in the cftr gene.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

merck sharp & dohme b.v. - elbasvir, grazoprevir - hepatitis c, krónikus - direct acting antivirals, antivirals for systemic use, antivirals for treatment of hcv infections - zepatier is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients 12 years of age and older who weigh at least 30 kg (see sections 4. 2, 4. 4 és 5. a hepatitis c vírus (hcv) genotípus specifikus tevékenység, lásd 4. 4 és 5.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - arthritis, rheumatoid - immunszuppresszánsok - 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). az olumiant monoterápiában vagy metotrexáttal kombinációban alkalmazható. 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.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

mcm vaccine b.v. - diftéria toxoidot tartalmazza, tetanusz toxoid, bordetella pertussis antigének: pertussis toxoid, rákok fonalas hemagglutinin, pertactin, fimbriae típusú, 2, 3, hepatitis b felületi antigén élesztősejtekben, poliovírus (inaktivált): írja be az 1 (mahoney), írja be a 2 (mef-1), 3-as típusú (saukett) előállított vero sejt/ b-típusú haemophilus influenzae poliszacharid (polyribosylribitol foszfát) konjugált meningococcus fehérje. - meningitis, haemophilus; poliomyelitis; tetanus; diphtheria; whooping cough; hepatitis b - a vakcinák - vaxelis (dtap-hb-ipv-hib) javallt elsődleges és emlékeztető oltás a csecsemők és a kisgyermekek, 6 hetes kortól diftéria, tetanusz, pertussis, hepatitis b, poliomyelitis és invazív betegségek okozta haemophilus influenzae b típus (hib). a vaxelis használatának összhangban kell lennie a hivatalos ajánlásokkal.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

zentiva, k.s. - pregabalin - anxiety disorders; epilepsy - antiepileptikumok, - neuropathic pain , pregabalin zentiva is indicated for the treatment of peripheral and central neuropathic pain in adults. , epilepsy , pregabalin zentiva is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. , generalised anxiety disorder , pregabalin zentiva is indicated for the treatment of generalised anxiety disorder (gad) in adults.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

medac gesellschaft fuer klinische spezialpraeparate mbh - asparagináz - prekurzorsejt limfoblasztikus leukémia-limfóma - daganatellenes szerek - spectrila a antineoplastic kombinációs terápia a kezelés az akut limfoblasztos leukémia (all) a gyermekgyógyászati betegek születéstől 18 év és a felnőttek elemeként szerepel.

Den europeiske union - ungarsk - EMA (European Medicines Agency)

ge healthcare as - mangafodipir trinátrium - mágneses rezonancia képalkotás - kontrasztanyag - ez a gyógyszer csak diagnosztikai célra használható. kontrasztanyag diagnosztikai mágneses rezonanciás képalkotás (mri) kimutatására elváltozások gyanúja esetén a máj az oka, hogy áttétes betegség vagy hepatocelluláris karcinóma. kiegészítőjeként, hogy mri, hogy segítse a nyomozást a központi hasnyálmirigy elváltozások.