Evropska unija - slovenščina - EMA (European Medicines Agency)

les laboratoires servier - pixantrone dimaleate - limfom, non-hodgkin - antineoplastična sredstva - zdravilo pixuvri je indicirano kot monoterapija za zdravljenje odraslih bolnikov z multiplo relapsnimi ali neodzivnimi agresivnimi limfomi brez hodgkinov b celic (nhl). prednost piksantona pri bolnikih, ki se uporabljajo kot pete ali večje kemoterapije pri bolnikih, ki so odporni na zadnjo terapijo.

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

krka, d.d., novo mesto - tietilperazin - raztopina za injiciranje - tietilperazin 6,5 mg / 1 ml - tietilperazin

Evropska unija - slovenščina - EMA (European Medicines Agency)

pharmaand gmbh - rucaparib camsylate - ovarijske neoplazme - antineoplastična sredstva - rubraca is indicated as monotherapy for the maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. rubraca je označen kot monotherapy za vzdrževanje zdravljenje odraslih bolnikov s platino-občutljive relapsed visoko-kakovostni razred epitelnih jajčnikov, fallopian tube, ali primarni trebušno raka, ki so v odziv (popolna ali delna) platinum, ki temelji kemoterapijo.

Evropska unija - slovenščina - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - cepiva - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Evropska unija - slovenščina - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - cepiva - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

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

sandoz d.d. - levprorelin - implantat - levprorelin 5 mg / 1 brizga - levprorelin

Evropska unija - slovenščina - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfin hidroklorid - opioidne motnje - druga zdravila na živčnem sistemu - sixmo je primerna za nadomestno zdravljenje odvisnosti od opioidov v klinično stabilno odraslih bolnikih, ki ne zahtevajo več kot 8 mg/dan sublingual buprenorfin, v okviru medicinske, socialne in psihološke obravnave.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitrombotična sredstva - brilique, co daje z acetilsalicilne kisline (asa), je označen za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih withacute koronarnih sindromov (acs), zdaj zgodovino miokardni infarkt (mi) in visokim tveganjem za razvoj atherothrombotic eventbrilique, co-daje z acetil salicilna kislina (asa), je označen za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih z anamnezo miokardni infarkt (mi je prišlo, najmanj eno leto nazaj) in visokim tveganjem za razvoj atherothrombotic dogodek.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - ticagrelor - peripheral vascular diseases; acute coronary syndrome - antitrombotična sredstva - possia, co-upravlja z acetilsalicilna kislina (asa), je indiciran za preprečevanje atherothrombotic dogodkov pri odraslih bolnikih z akutni koronarni sindrom (nestabilna angina pektoris, non-st-infarkta miokarda [nstemi] ali st-nadmorske višine miokardni infarkt [stemi]); vključno z bolniki, ki upravlja z zdravili, in tistih, ki so z perkutano koronarno intervencijo (pci) ali koronarne arterije cepljenje obvod (cabg).

Evropska unija - slovenščina - EMA (European Medicines Agency)

accord healthcare s.l.u. - apixaban - venous thromboembolism; stroke; arthroplasty - antitrombotična sredstva - prevention of venous thromboembolic events (vte) in adult patients who have undergone elective hip or knee replacement surgery. preprečevanje kapi in sistemska embolija pri odraslih bolnikih z ne-valvular atrijsko fibrilacijo (nvaf), z eno ali več dejavnikov tveganja, kot so pred možgansko kap ali prehodni ischaemic napad (tia); starost ≥ 75 let; hipertenzija; sladkorna bolezen; simptomatsko srčno popuščanje (nyha razred ≥ ii). zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih (glej poglavje 4. 4 za haemodynamically nestabilno pe bolnikov). prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (nvaf), with one or more risk factors, such as prior stroke or transient ischaemic attack (tia); age≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (nyha class ≥ ii). zdravljenje globoke venske tromboze (dvt) in pljučna embolija (pe), in preprečevanje ponavljajočih se dvt in pe pri odraslih (glej poglavje 4. 4 za haemodynamically nestabilno pe bolnikov).