ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunszuppresszánsok - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

sfl pharmaceuticals deutschland gmbh - nyxthracis - anthrax - immunrendszer sera, immunglobulinok, - obiltoxaximab sfl is indicated in combination with appropriate antibacterial drugs in all age groups for treatment of inhalational anthrax due to bacillus anthracis (see section 5. obiltoxaximab sfl is indicated in all age groups for post-exposure prophylaxis of inhalational anthrax when alternative therapies are not appropriate or are not available (see section 5.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

astrazeneca ab - moxetumomab pasudotox - leukémia, szőrös sejt - daganatellenes szerek - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - gastrointestinal stromal tumorok - daganatellenes szerek - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - daganatellenes szerek - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.

হাঙ্গেরি - হাঙ্গেরীয় - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

fresenius kabi ab, uppsala - alanine; arginine; glycine; histidine; isoleucine; leucine; lysine acetate; methionine; phenylalanine; proline; serine; taurine; threonine; tryptophan; tyrosine; valine; calcium chloride dihydrate; magnesium sulfate heptahydrate; potassium chloride; sodium acetate trihydrate; zinc sulphate heptahydrate; glucose monohydrate; soya-bean oil refined; triglycerides medium chain; sodium glycerophosphate hydrated -

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

oncopeptides ab - melphalan flufenamide hydrochloride - myeloma multiplex - daganatellenes szerek - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - cytomegalovirus fertőzések - vírusellenes szerek szisztémás alkalmazásra - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). figyelembe kell venni hivatalos útmutató a megfelelő használatára a vírusellenes szerek.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

amryt pharmaceuticals dac - octreotide acetate - acromegalia - hipofízis és hypothalamus hormonok és analógok - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

ইউরোপীয় ইউনিয়ন - হাঙ্গেরীয় - EMA (European Medicines Agency)

mirum pharmaceuticals international b.v. - maralixibat chloride - alagille syndrome - other drugs for bile therapy - livmarli is indicated for the treatment of cholestatic pruritus in patients with alagille syndrome (algs) 2 months of age and older.