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

krka, d.d., novo mesto - omeprazol - prašek za raztopino za injiciranje/infundiranje - omeprazol 40 mg / 1 viala - omeprazol

Evropska unija - slovenščina - EMA (European Medicines Agency)

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. glej poglavja 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Evropska unija - slovenščina - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastična sredstva - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Evropska unija - slovenščina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - antineoplastična sredstva - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

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

pfizer luxembourg sarl - alprostadil - prašek in vehikel za raztopino za injiciranje - alprostadil 23,5 µg / 1 viala - alprostadil

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

pfizer luxembourg sarl - alprostadil - prašek in vehikel za raztopino za injiciranje - alprostadil 11,9 µg / 1 viala - alprostadil

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

pfizer luxembourg sarl - doksiciklin - disperzibilna tableta - doksiciklin 100 mg / 1 tableta - doksiciklin

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

pfizer luxembourg sarl - doksiciklin - disperzibilna tableta - doksiciklin 100 mg / 1 tableta - doksiciklin

Evropska unija - slovenščina - EMA (European Medicines Agency)

gilead sciences international ltd  - emtricitabine, rilpivirine hydrochloride, tenofovir disoproxil fumarate - okužbe z virusom hiv - antivirusi za sistemsko uporabo - eviplera je indicirano za zdravljenje odraslih, okuženih z virusom človeške imunske pomanjkljivosti tipa 1 (hiv-1) brez znane mutacije, povezane z odpornostjo-nukleozidni reverzne transkriptaze (nnrti) inhibitor razred, so ali emtricitabine, in z virusna obremenitev ≤ 100.000 hiv-1 rna kopij/ml. kot pri drugih protiretrovirusnih zdravilih je treba testiranje genotipske odpornosti in / ali zgodovinske podatke o odpornosti voditi pri uporabi zdravila eviplera.

Evropska unija - slovenščina - EMA (European Medicines Agency)

vétoquinol sa - torasemid brezvodni - sulfonamide, golo, visoko-strop diuretiki - psi - za zdravljenje kliničnih znakov, vključno z edemom in izlivom, povezanih s kongestivnim srčnim popuščanjem pri psih.