Valaciklovir Arrow 500 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

valaciklovir arrow 500 mg filmsko obložene tablete

arrow generics limited - valaciklovir - filmsko obložena tableta - valaciklovir 500 mg / 1 tableta - valaciklovir

Valsartan Arrow 80 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

valsartan arrow 80 mg filmsko obložene tablete

arrow generics limited - valsartan - filmsko obložena tableta - valsartan 80 mg / 1 tableta - valsartan

Pemazyre Evropska unija - slovenščina - EMA (European Medicines Agency)

pemazyre

incyte biosciences distribution b.v. - pemigatinib - cholangiocarcinoma - antineoplastična sredstva - pemazyre monotherapy is indicated for the treatment of adults with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed  after at least one prior line of systemic therapy.

Lumykras Evropska unija - slovenščina - EMA (European Medicines Agency)

lumykras

amgen europe bv - sotorasib - karcinom, pljučni pljuč - antineoplastična sredstva - lumykras as monotherapy is indicated for the treatment of adults with advanced non-small cell lung cancer (nsclc) with kras g12c mutation and who have progressed after at least one prior line of systemic therapy.

Lytgobi Evropska unija - slovenščina - EMA (European Medicines Agency)

lytgobi

taiho pharma netherlands b.v. - futibatinib - cholangiocarcinoma - zdravila z delovanjem na novotvorbe agenti - lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.

Orserdu Evropska unija - slovenščina - EMA (European Medicines Agency)

orserdu

stemline therapeutics b.v. - elacestrant - neoplazme dojke - endokrini terapija - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

Descovy Evropska unija - slovenščina - EMA (European Medicines Agency)

descovy

gilead sciences ireland uc - emtricitabine, tenofovir alafenamide - okužbe z virusom hiv - antivirusi za sistemsko uporabo - descovy is indicated in combination with other antiretroviral agents for the treatment of adults and adolescents (aged 12 years and older with body weight at least 35 kg) infected with human immunodeficiency virus type 1 (hiv-1).

Vemlidy Evropska unija - slovenščina - EMA (European Medicines Agency)

vemlidy

gilead sciences ireland uc - tenofovir alafenamid fumarat - hepatitis b - antivirusi za sistemsko uporabo - vemlidy is indicated for the treatment of chronic hepatitis b (chb) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.

Kaftrio Evropska unija - slovenščina - EMA (European Medicines Agency)

kaftrio

vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - cistična fibroza - drugi proizvodi dihal - kaftrio is indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (cf) in patients aged 6 years and older who have at least one f508del mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene.

Calquence Evropska unija - slovenščina - EMA (European Medicines Agency)

calquence

astrazeneca ab - acalabrutinib - levkemija, limfocitna, kronična, b-celica - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.