Ngenla Europäische Union - Slowenisch - EMA (European Medicines Agency)

ngenla

pfizer europe ma eeig - somatrogon - growth and development - hipofiza in hypothalamic hormoni in analogi - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Oxbryta Europäische Union - Slowenisch - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Dimethyl fumarate Polpharma Europäische Union - Slowenisch - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetil fumarat - multiplo sklerozo, recidivno-nakazila - imunosupresivi - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Camcevi Europäische Union - Slowenisch - EMA (European Medicines Agency)

camcevi

accord healthcare s.l.u. - leuprorelin mesilate - prostatične neoplazme - endokrini terapija - camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

Sorafenib Accord Europäische Union - Slowenisch - EMA (European Medicines Agency)

sorafenib accord

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastična sredstva - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

Bimervax Europäische Union - Slowenisch - 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 - cepiva - 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.

Remifentanil Kabi 1 mg prašek za koncentrat za raztopino za injiciranje ali infundiranje Slowenien - Slowenisch - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

remifentanil kabi 1 mg prašek za koncentrat za raztopino za injiciranje ali infundiranje

fresenius kabi deutschland gmbh - remifentanil - prašek za koncentrat za raztopino za injiciranje/infundiranje - remifentanil 1 mg / 1 viala - remifentanil

Fluorouracil Accord 50 mg/ml raztopina za injiciranje/infundiranje Slowenien - Slowenisch - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

fluorouracil accord 50 mg/ml raztopina za injiciranje/infundiranje

accord healthcare - fluorouracil - raztopina za injiciranje/infundiranje - fluorouracil 50 mg / 1 ml - fluorouracil

Fluorouracil Accord 50 mg/ml raztopina za injiciranje/infundiranje Slowenien - Slowenisch - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

fluorouracil accord 50 mg/ml raztopina za injiciranje/infundiranje

accord healthcare - fluorouracil - raztopina za injiciranje/infundiranje - fluorouracil 50 mg / 1 ml - fluorouracil

Ceftazidim Hospira 1 g prašek za raztopino za injiciranje/infundiranje Slowenien - Slowenisch - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

ceftazidim hospira 1 g prašek za raztopino za injiciranje/infundiranje

hospira uk ltd - ceftazidim - prašek za raztopino za injiciranje/infundiranje - ceftazidim 1000 mg / 1 viala - ceftazidim