Jemperli Europska Unija - hrvatski - EMA (European Medicines Agency)

jemperli

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.

PANCILLIN 200000 i.j./1 boca+ 600000 i.j./1 boca prašak za suspenziju za injekciju Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

pancillin 200000 i.j./1 boca+ 600000 i.j./1 boca prašak za suspenziju za injekciju

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - benzilpenicilinnatrijum, benzilpenicilinprokain - prašak za suspenziju za injekciju - 200000 i.j./1 boca+ 600000 i.j./1 boca - 1 bočica sa praškom za suspenziju za injekciju sadrži: 800 000 i.j. benzilpenicilina, što predstavlja smjesu od 200 000 i.j. benzilpenicilinnatrijuma + 600 000 i.j. benzilpenicilin, prokaina

Lutetium (177Lu) chloride Billev (previously Illuzyce) Europska Unija - hrvatski - EMA (European Medicines Agency)

lutetium (177lu) chloride billev (previously illuzyce)

billev pharma aps - lutetium (177lu) chloride - radionuklidno slikanje - terapeutski radiofarmaceutski pripravci - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.

Locametz Europska Unija - hrvatski - EMA (European Medicines Agency)

locametz

novartis europharm limited  - gozetotide - radionuklidno slikanje - dijagnostički radiofarmaceutici - ovaj je lijek samo za dijagnostičku uporabu. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.