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

actavis group ptc ehf. - citalopram - filmsko obložena tableta - citalopram 10 mg / 1 tableta - citalopram

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

actavis group ptc ehf. - citalopram - filmsko obložena tableta - citalopram 40 mg / 1 tableta - citalopram

Evropska unija - slovenščina - EMA (European Medicines Agency)

recordati rare diseases - pasireotid - acromegaly; pituitary acth hypersecretion - hipofize in hipotalamični hormoni in analogi - zdravilo signifor je indicirano za zdravljenje odraslih bolnikov s cushingovo boleznijo, za katere operacija ni možna ali za katero operacija ni uspela. signifor je indiciran za zdravljenje odraslih bolnikov z acromegaly, za katere kirurgija ni opcija ali ni bil zdravljenja in ki so neustrezno nadzorovano na zdravljenje z drugim somatostatin analogni.

Evropska unija - slovenščina - EMA (European Medicines Agency)

diurnal europe b.v. - hidrokortizon - nadledvična insuficienca - kortikosteroidi za sistemsko uporabo - zamenjava terapije nadledvične žleze, cerebrovaskularnih pri dojenčkih, otrocih in mladostnikih (od rojstva do < 18 let).

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

metirapon - kapsula, mehka - metirapon 250 mg / 1 ml - metirapon

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

posakonazol - gastrorezistentna tableta - posakonazol 100 mg / 1 tableta - posakonazol

Evropska unija - slovenščina - EMA (European Medicines Agency)

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - antineoplastična sredstva - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. bolniki, ki imajo nizko ali zelo nizko tveganje za ponovitev, ne bi smel imeti adjuvant treatment. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. razen v novo diagnozo kronične faze cml, ni kontroliranih preskušanjih, dokazujejo kliničnih koristi ali poveča preživetje pri teh bolezni.

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

lek d.d. - oksikodon - tableta s podaljšanim sproščanjem - oksikodon 17,9 mg / 1 tableta - oksikodon

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

lek d.d. - oksikodon - tableta s podaljšanim sproščanjem - oksikodon 4,5 mg / 1 tableta - oksikodon

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

lek d.d. - oksikodon - tableta s podaljšanim sproščanjem - oksikodon 9 mg / 1 tableta - oksikodon