Clivarin 1432 i.e. anti-Xa/0,25 ml raztopina za injiciranje Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

clivarin 1432 i.e. anti-xa/0,25 ml raztopina za injiciranje

abbott laboratories d.o.o. - natrijev reviparinat - raztopina za injiciranje - natrijev reviparinat 1432 anti-xa i.e. / 0,25 ml - reviparin

Clivarin 3436 i.e. anti-Xa/0,6 ml raztopina za injiciranje Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

clivarin 3436 i.e. anti-xa/0,6 ml raztopina za injiciranje

abbott laboratories d.o.o. - natrijev reviparinat - raztopina za injiciranje - natrijev reviparinat 3436 anti-xa i.e. / 0,6 ml - reviparin

Clivarin 5726 i.e. anti-Xa/ml raztopina za injiciranje Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

clivarin 5726 i.e. anti-xa/ml raztopina za injiciranje

abbott laboratories d.o.o. - natrijev reviparinat - raztopina za injiciranje - natrijev reviparinat 5726 anti-xa i.e. / 1 ml - reviparin

Kresflo 125 mikrogramov/vpih inhalacijska suspenzija pod tlakom Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kresflo 125 mikrogramov/vpih inhalacijska suspenzija pod tlakom

momaja s.r.o. - flutikazonpropionat - inhalacijska suspenzija pod tlakom - flutikazonpropionat 125 µg / 1 vpih - flutikazon

Kresflo 250 mikrogramov/vpih inhalacijska suspenzija pod tlakom Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

kresflo 250 mikrogramov/vpih inhalacijska suspenzija pod tlakom

momaja s.r.o. - flutikazonpropionat - inhalacijska suspenzija pod tlakom - flutikazonpropionat 250 µg / 1 vpih - flutikazon

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

prostamol mehke kapsule

clinres farmacija d.o.o. - ekstrakt plodu palmeta - kapsula, mehka - ekstrakt plodu palmeta 320 mg / 1 kapsula - plod palmeta

Ekstrakt plodu palmeta Clinres Farmacija mehke kapsule Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

ekstrakt plodu palmeta clinres farmacija mehke kapsule

clinres farmacija d.o.o. - ekstrakt plodu palmeta - kapsula, mehka - ekstrakt plodu palmeta 320 mg / 1 kapsula - plod palmeta

Kymriah Evropska unija - slovenščina - EMA (European Medicines Agency)

kymriah

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - drugi antineoplastiki - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Abecma Evropska unija - slovenščina - EMA (European Medicines Agency)

abecma

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastična sredstva - abecma is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Carvykti Evropska unija - slovenščina - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multiple myeloma - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.