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

krka, d.d., novo mesto - mikonazol - oralni gel - mikonazol 20 mg / 1 g - mikonazol

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

accord healthcare - ritonavir - filmsko obložena tableta - ritonavir 100 mg / 1 kapsula - ritonavir

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

accord healthcare - ritonavir - filmsko obložena tableta - ritonavir 100 mg / 1 kapsula - ritonavir

Evropska unija - slovenščina - EMA (European Medicines Agency)

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - antineoplastična sredstva - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.

Evropska unija - slovenščina - EMA (European Medicines Agency)

ipsen pharma - cabozantinib - Širokopasemske neoplazme - antineoplastična sredstva - zdravljenje odraslih bolnikov s progresivnim, neresektabilnim lokalno napredovalim ali metastatskim medularnim karcinomom ščitnice.

Evropska unija - slovenščina - EMA (European Medicines Agency)

gedeon richter ltd  - ulipristal acetat - leiomyoma - spolni hormoni in zdravila genitalni sistem, - ulipristalacetat je indiciran za predoperativno zdravljenje zmernih do hudih simptomov materničnih fibroidov pri odraslih ženskah v reproduktivni dobi. ulipristal acetata je primerna za občasno zdravljenje zmerne do hude simptome maternice fibroids v odrasle ženske v rodni dobi.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - osimertinib mesilate - karcinom, pljučni pljuč - druga zdravila z delovanjem na novotvorbe agenti, protein kinaza inhibitorji - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Evropska unija - slovenščina - EMA (European Medicines Agency)

gedeon richter plc. - ulipristal acetat - leiomyoma - spolni hormoni in zdravila genitalni sistem, - ulipristal acetata, ki je navedena za eno zdravljenje, seveda pre-operative zdravljenje zmerne do hude simptome maternice fibroids v odrasle ženske v rodni dobi. ulipristal acetata je primerna za občasno zdravljenje zmerne do hude simptome maternice fibroids v izobraževanje žensk v rodni dobi, ki niso primerni za operacijo.

Evropska unija - slovenščina - EMA (European Medicines Agency)

eigerbio europe limited - lonafarnib - progeria; laminopathies - drugi zdravljene bolezni prebavil in presnove izdelki, - zokinvy is indicated for the treatment of patients 12 months of age and older with a genetically confirmed diagnosis of hutchinson-gilford progeria syndrome or a processing-deficient progeroid laminopathy associated with either a heterozygous lmna mutation with progerin-like protein accumulation or a homozygous or compound heterozygous zmpste24 mutation.

Evropska unija - slovenščina - EMA (European Medicines Agency)

takeda pharma a/s - alogliptin, pioglitazone - diabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - incresync is indicated as a second- or third-line treatment in adult patients aged 18 years and older with type-2 diabetes mellitus: , as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on pioglitazone alone, and for whom metformin is inappropriate due to contraindications or intolerance;, in combination with metformin (i. trojna kombinacija terapija), kot dodatek k prehrani in vadbi za izboljšanje glycaemic nadzor pri odraslih bolnikih (zlasti prekomerno telesno težo bolnikov) neustrezno nadzorovano na maksimalno dopustne odmerek metforminom in pioglitazone. poleg tega incresync mogoče zamenjati ločenih tablet alogliptin in pioglitazone v tistih odraslih bolnikih, starih 18 let in starejših s tipa 2 sladkorna bolezen že zdravijo s to kombinacijo. po začetku terapije z incresync, bolnike je treba pregledati in po treh do šestih mesecih, da oceni ustreznost odziva na zdravljenje (e. zmanjšanje hba1c). pri bolnikih, ki ne kažejo ustrezen odgovor, incresync, je treba prekiniti,. v luči možnih tveganj z daljšo pioglitazone terapije, predpisovalce morajo potrditi na kasnejše redne preglede, da je korist incresync je ohranjena (glej poglavje 4.