Slovenja - Sloven - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kemofarmacija d.d. - alendronska kislina - filmsko obložena tableta - alendronska kislina 70 mg / 1 tableta - alendronska kislina

Slovenja - Sloven - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kemofarmacija d.d. - alendronska kislina - filmsko obložena tableta - alendronska kislina 70 mg / 1 tableta - alendronska kislina

Slovenja - Sloven - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kemofarmacija d.d. - askorbinska kislina (vitamin c); baker; biotin (vitamin h); cianokobalamin (vitamin b12); cink; vseracemni-alfa-tokoferilacetat; folna kislina (vitamin b9); holekalciferol (vitamin d3); kalcij; lecitin; magnezij; mangan; nikotinamid; piridoksinijev klorid; riboflavin (vitamin b2); selen; suhi ekstrakt korenine pravega ginsenga g115, standardizirani; tiaminijev nitrat; železo; retinolpalmitat - kapsula, mehka - askorbinska kislina (vitamin c) 60 mg / 1 kapsula  baker2 mg / 1 kapsula  biotin (vitamin h)0,15 mg / 1 kapsula  cianokobalamin (vitamin b12)0,001 mg / 1 kapsula  cink1 mg / 1 kapsula  vseracemni-alfa-tokoferilacetat14,9 mg / 1 kapsula  folna kislina (vitamin b9)0,1 mg / 1 kapsula  holekalciferol (vitamin d3)200 mg / 1 kapsula  kalcij100 mg / 1 kapsula  lecitin100 mg / 1 kapsula  magnezij10 mg / 1 kapsula  mangan2,5 mg / 1 kapsula  nikotinamid18 mg / 1 kapsula  piridoksinijev klorid2 mg / 1 kapsula  riboflavin (vitamin b2)1,6 mg / 1 kapsula  selen0,05 mg / 1 kapsula  suhi ekstrakt korenine pravega ginsenga g115, standardizirani40 mg / 1 kapsula  tiaminijev nitrat1,4 mg / 1 kapsula  železo10 mg / 1 kapsula  retinolpalmitat0,8009 mg / 1 kapsula; baker 2 mg / 1 kapsula  biotin (vitamin h)0,15 mg / 1 kapsula  cianokobalamin (vitamin b12)0,001 mg / 1 kapsula  cink1 mg / 1 kapsula  vseracemni-alfa-tokoferilacetat14,9 mg / 1 kapsula  folna kislina (vitamin b9)0,1 mg / 1 kapsula  holekalciferol (vitamin d3)200 mg / 1 kapsula  kalcij100 mg / 1 kapsula  lecitin100 mg / 1 kapsula  magnezij10 mg / 1 kapsula  mangan2,5 mg / 1 kapsula  nikotinamid18 mg / 1 kapsula  piridoksinijev klorid2 mg / 1 kapsula  riboflavin (vitamin b2)1,6 mg / 1 kapsula  selen0,05 mg / 1 kapsula  suhi ekstrakt korenine pravega ginsenga g115, standardizirani40 mg / 1 kapsula  tiaminijev nitrat1,4 mg / 1 kapsula  železo10 mg / 1 kapsula  retinolpalmitat0,8009 mg / 1 kapsula; biotin (vitamin h) 0,15 mg / 1 kapsula  cianokobalamin (vitamin b12)0,001 mg / 1 kapsula  cink1 mg / 1 kapsula  vseracemni-alfa-tokoferilacetat14,9 mg / 1 kapsula  folna kislina (vitamin b9)0,1 mg / 1 kapsula  holekalciferol (vitamin d3)200 mg / 1 kapsula  kalcij100 mg / 1 kapsula  lecitin100 mg / 1 kapsula  magnezij - multivitamini in drugi minerali ter kombinacije

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

photonamic gmbh & co. kg - 5-aminolevulinična kislina hidroklorid - glioma - antineoplastična sredstva - gliolan je indiciran pri odraslih bolnikih za vizualizacijo malignih tkiv med operacijo malignih glioma (iii. in iv. svetovna zdravstvena organizacija).

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

ge healthcare b.v. - ioflupan (123l) - tomography, emission-computed, single-photon; lewy body disease; parkinson disease; alzheimer disease - diagnostični radiofarmacevtiki - to zdravilo je samo za diagnostično uporabo. datscan je označen za odkrivanje izguba funkcionalne dopaminergičnih nevronov terminalov v striatum:pri odraslih bolnikih s klinično negotova parkinsonian sindromov, na primer tistih z zgodnji simptomi, da bi razlikuje bistveno, tremor iz parkinsonian sindromov, povezanih z idiopatsko parkinsonovo boleznijo, bolezni, multiple sistemske atrofije in postopno supranuclear palsy. datscan se ne more razlikovati med parkinsonove bolezni, multiple sistemske atrofije in postopno supranuclear palsy. pri odraslih bolnikih, za pomoč pri razlikovanju verjetno, demenco z lewy organe, od alzheimerjeve bolezni. datscan se ne more razlikovati med demenco z lewy organov in parkinsonova bolezen, demenca.

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

merck sharp and dohme b.v - posakonazol - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimikotiki za sistemsko uporabo - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 in 5. 1):- invasive aspergillosisnoxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections  4. 2 in 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. refractoriness je opredeljena kot napredovanje okužbe ali neuspeh za izboljšanje po najmanj 7 dni pred terapevtskih odmerkih učinkovito protiglivično zdravljenje. noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4. 2 in 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 in 5. 1):- invasive aspergillosisnoxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adult and paediatric patients from 2 years of age (see sections 4. 2 in 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. refractoriness je opredeljena kot napredovanje okužbe ali neuspeh za izboljšanje po najmanj 7 dni pred terapevtskih odmerkih učinkovito protiglivično zdravljenje. noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in the following adult and paediatric patients from 2 years of age (see sections 4. 2 in 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease (gvhd) and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age (see sections 4. 2 in 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. refractoriness je opredeljena kot napredovanje okužbe ali neuspeh za izboljšanje po najmanj 7 dni pred terapevtskih odmerkih učinkovito protiglivično zdravljenje. noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2  years of age:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high  risk of developing invasive fungal infections;- haematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high  risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5. 1):- invazivne aspergillosis pri bolnikih z boleznijo, ki je neodzivna, da amphotericin b ali itraconazole ali pri bolnikih, ki ne prenašajo teh zdravil;- fusariosis pri bolnikih z boleznijo, ki je neodzivna, da amphotericin b ali pri bolnikih, ki so nestrpne amphotericin b;- chromoblastomycosis in mycetoma pri bolnikih z boleznijo, ki je neodzivna, da itraconazole ali pri bolnikih, ki so nestrpne itraconazole;- coccidioidomycosis pri bolnikih z boleznijo, ki je neodzivna, da amphotericin b, itraconazole ali fluconazole ali pri bolnikih, ki ne prenašajo teh zdravil;- Žrela kandidoza: kot prvo linijo zdravljenja pri bolnikih, ki imajo hude bolezni ali so immunocompromised, v kateri je odziv na aktualne terapija je pričakovati, da bo slaba. refractoriness je opredeljena kot napredovanje okužbe ali neuspeh za izboljšanje po najmanj 7 dni pred terapevtskih odmerkih učinkovito protiglivično zdravljenje. noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis.

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

menarini international operations luxembourg s.a. (miol) - febuksostat - protin - antigout pripravki - 80 mg alkohola:zdravljenje kronične hyperuricaemia v razmerah, v katerih urate nanašanja je že prišlo do (vključno z zgodovino, ali prisotnost, tophus in/ali uričnega artritisa). adenuric je navedeno v odrasli. 120 mg alkohola:adenuric je indiciran za zdravljenje kronične hyperuricaemia v razmerah, v katerih urate nanašanja je že prišlo do (vključno z zgodovino, ali prisotnost, tophus in/ali uričnega artritisa). adenuric je indicirano za preprečevanje in zdravljenje hyperuricaemia pri odraslih bolnikih kemoterapijo za haematologic malignancies na srednje do visoko tveganje za tumor lysis sindrom (tls). adenuric je navedeno v odrasli.

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimikotiki za sistemsko uporabo - treatment of invasive candidiasis in adult or paediatric patients;treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin b, lipid formulations of amphotericin b and / or itraconazole. refractoriness is defined as progression of infection or failure to improve after a minimum of seven days of prior therapeutic doses of effective antifungal therapy;empirical therapy for presumed fungal infections (such as candida or aspergillus) in febrile, neutropaenic adult or paediatric patients.

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

pfizer limited - insulin human - sladkorna bolezen - zdravila, ki se uporabljajo pri diabetesu - exubera je indiciran za zdravljenje odraslih bolnikov z diabetesom tipa 2, bolezni notadequately nadzira z ustno antidiabetic sredstva in potrebujejo insulin terapija. exubera je prikazano tudi za zdravljenje odraslih bolnikih s tipom 1 sladkorne bolezni, inaddition za dolgo ali vmesne deluje podkožnega insulina, za katere potencialne koristi ofadding pri vdihavanju insulina odtehtajo morebitne pomisleke glede varnosti (glej poglavje 4.

Unjoni Ewropea - Sloven - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - irbesartan, hydrochlorothiazide - hipertenzija - sredstva, ki delujejo na sistem renin-angiotenzin - zdravljenje esencialne hipertenzije. ta fiksni odmerek kombinacija je označena pri odraslih bolnikih, katerih krvni tlak ni ustrezno nadzorovan na irbesartan ali hydrochlorothiazide sami (glej poglavje 5.