Evropska unija - slovenščina - EMA (European Medicines Agency)

pfizer europe ma eeig - gemtuzumab ozogamicin - leukemija, myeloid, akutna - antineoplastična sredstva - mylotarg je označen za kombiniranega zdravljenja z daunorubicin (dnr) in cytarabine (arac) za zdravljenje bolnikov v starosti 15 let in več s predhodno nezdravljenih, de novo cd33-pozitivno akutno mieloično levkemijo (aml), razen akutna promyelocytic levkemijo (apl).

Evropska unija - slovenščina - EMA (European Medicines Agency)

bluebird bio (netherlands) b.v. - autologous cd34+ celic, obogaten prebivalstva, ki vsebuje hematopoietic izvornih celic transduced z lentiglobin bb305 lentiviral vektor kodiranje beta-a-t87q-globin gena - beta-talasemija - other hematological agents - zynteglo je indiciran za zdravljenje bolnikov, 12 let in več, s transfuzijo, ki je odvisna β talasemija (tdt), ki nimajo β0/β0 genotip, za katere haematopoietic stem cell (hsc) presaditev, je primerno, ampak človeško leukocyte antigen (hla) ujema povezane hsc donatorjev ni na voljo.

Evropska unija - slovenščina - EMA (European Medicines Agency)

cis bio international - ioflupan (123l) - radionuclide imaging; dementia; movement disorders - diagnostični radiofarmacevtiki - to zdravilo je samo za diagnostično uporabo. striascan je označen za odkrivanje izguba funkcionalne dopaminergičnih nevronov terminalov v striatum:pri odraslih bolnikih s klinično negotova parkinsonian sindromov, na primer tistih z zgodnji simptomi, da bi razlikuje bistveno, tremor iz parkinsonian sindromov, povezanih z idiopatsko parkinsonovo boleznijo, bolezni, multiple sistemske atrofije in postopno supranuclear palsy. striascan, ne more razlikovati med parkinsonove bolezni, multiple sistemske atrofije in postopno supranuclear palsy. pri odraslih bolnikih, za pomoč pri razlikovanju verjetno, demenco z lewy organe, od alzheimerjeve bolezni. striascan, ne more razlikovati med demenco z lewy organov in parkinsonova bolezen, demenca.

Evropska unija - slovenščina - EMA (European Medicines Agency)

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antineoplastična sredstva - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

Evropska unija - slovenščina - EMA (European Medicines Agency)

ultragenyx germany gmbh - evinacumab - hiperholesterolemija - sredstva za spreminjanje lipidov - evkeeza is indicated as an adjunct to diet and other low-density lipoprotein-cholesterol (ldl-c) lowering therapies for the treatment of adult and adolescent patients aged 12 years and older with homozygous familial hypercholesterolaemia (hofh).

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013; ha seva a/darwin/6/2021, ivr-227, podoben sevu a/darwin/9/2021 (h3n2); ha seva b/austria/1359417/2021, bvr-26, podoben sevu b/austria/1359417/2021; ha seva a/victoria/2897/2022, ivr-238, podoben sevu a/victoria/4897/2022 (h1n1)p - suspenzija za injiciranje v napolnjeni injekcijski brizgi - ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013 15 µg / 0,5 ml  ha seva a/darwin/6/2021, ivr-227, podoben sevu a/darwin/9/2021 (h3n2)15 µg / 0,5 ml  ha seva b/austria/1359417/2021, bvr-26, podoben sevu b/austria/1359417/202115 µg / 0,5 ml  ha seva a/victoria/2897/2022, ivr-238, podoben sevu a/victoria/4897/2022 (h1n1)p15 µg / 0,5 ml; ha seva a/darwin/6/2021, ivr-227, podoben sevu a/darwin/9/2021 (h3n2) 15 µg / 0,5 ml  ha seva b/austria/1359417/2021, bvr-26, podoben sevu b/austria/1359417/202115 µg / 0,5 ml  ha seva a/victoria/2897/2022, ivr-238, podoben sevu a/victoria/4897/2022 (h1n1)p15 µg / 0,5 ml; ha seva b/austria/1359417/2021, bvr-26, podoben sevu b/austria/1359417/2021 15 µg / 0,5 ml  ha seva a/victoria/2897/2022, ivr-238, podoben sevu a/victoria/4897/2022 (h1n1)p15 µg / 0,5 ml; ha seva a/victoria/2897/2022, ivr-238, podoben sevu a/victoria/4897/2022 (h1n1)p - cepivo proti gripi, z delci virusov ali s površinskimi antigeni, inaktivirano

Evropska unija - slovenščina - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - spesolimab - psoriaza - imunosupresivi - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

Evropska unija - slovenščina - EMA (European Medicines Agency)

novartis europharm limited - tislelizumab - esophageal squamous cell carcinoma - antineoplastična sredstva - oesophageal squamous cell carcinoma (oscc) tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic oesophageal squamous cell carcinoma after prior platinum-based chemotherapy.