Elonva Unia Europejska - polski - EMA (European Medicines Agency)

elonva

n.v. organon - corifollitropin alfa - reproductive techniques, assisted; ovulation induction; investigative techniques - hormony płciowe i modulatory układu rozrodczego, - controlled ovarian stimulation (cos) in combination with a gnrh antagonist for the development of multiple follicles in women participating in an assisted reproductive technology (art) program. elonva is indicated for the treatment of adolescent males (14 to less than 18 years and older) with hypogonadotropic hypogonadism, in combination with human chorionic gonadotropin (hcg).

Insulatard Unia Europejska - polski - EMA (European Medicines Agency)

insulatard

novo nordisk a/s - insulin human - cukrzyca - leki stosowane w cukrzycy - leczenie cukrzycy.

Kogenate Bayer Unia Europejska - polski - EMA (European Medicines Agency)

kogenate bayer

bayer ag  - octocog alfa - hemofilia - antykrościeryczne - leczenie i profilaktyka krwawień u pacjentów z hemofilią a (wrodzony niedobór czynnika viii). ten lek nie zawiera czynnika von willebranda i dlatego nie zaznaczono w willebranda .

Mixtard Unia Europejska - polski - EMA (European Medicines Agency)

mixtard

novo nordisk a/s - insulin human - cukrzyca - leki stosowane w cukrzycy - leczenie cukrzycy.

Protaphane Unia Europejska - polski - EMA (European Medicines Agency)

protaphane

novo nordisk a/s - insulin human - cukrzyca - leki stosowane w cukrzycy - leczenie cukrzycy.

Insuman Unia Europejska - polski - EMA (European Medicines Agency)

insuman

sanofi-aventis deutschland gmbh - insulin human - cukrzyca - leki stosowane w cukrzycy - cukrzyca wymaga leczenia insuliną. preparat insuman rapid nadaje się również do leczenia śpiączki hiperglikemicznej i kwasicy ketonowej, a także do stabilizacji przed-, wewnątrz- i pooperacyjnej u pacjentów z cukrzycą.

Inpremzia Unia Europejska - polski - EMA (European Medicines Agency)

inpremzia

baxter holding b.v. - insulin human (rdna) - cukrzyca - leki stosowane w cukrzycy - inpremzia is indicated for the treatment of diabetes mellitus.

Bimervax Unia Europejska - polski - EMA (European Medicines Agency)

bimervax

hipra human health s.l. - sars-cov-2 virus recombinant spike (s) protein receptor binding domain (rbd) fusion heterodimer – b.1.351-b.1.1.7 strains - covid-19 virus infection - szczepionki - bimervax is indicated as a booster for active immunisation to prevent covid-19 in individuals 16 years of age and older who have previously received a mrna covid-19 vaccine.

Flebogamma DIF (previously Flebogammadif) Unia Europejska - polski - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - immunoglobuliny ludzkiej normalnej - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - odporne surowicy i immunoglobuliny, - 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.

Kymriah Unia Europejska - polski - EMA (European Medicines Agency)

kymriah

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - inne środki przeciwnowotworowe - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.