Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

pliva d.o.o.sarajevo - bortezomib - prašak za otopinu za injekciju - 3,5 mg/1 bočica - 1 bočica praška za otopinu za injekciju sadrži: 3,5 mg bortezomiba ( u obliku estera boronatne kiseline i manitola)

Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - bortezomib - rastvor za injekciju - 2,5 mg/1 ml - 1 ml rastvora za injekciju sadrži: 2,5 mg bortezomiba

Europska Unija - hrvatski - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - multipli mijelom - 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.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

ever valinject gmbh, oberburgau 3, unterach am attersee, austrija - бортезомиб - otopina za injekciju - urbroj: 1 ml otopine za injekciju sadrži 2,5 mg bortezomiba (u obliku estera boronatne kiseline i manitola) jedna bočica s 1 ml otopine za injekciju sadrži 2,5 mg bortezomiba (u obliku estera boronatne kiseline i manitola) jedna bočica s 1,4 ml otopine za injekciju sadrži 3,5 mg bortezomiba (u obliku estera boronatne kiseline i manitola)

Europska Unija - hrvatski - EMA (European Medicines Agency)

lipomed gmbh - Талидомид - multipli mijelom - imunosupresivi - thalidomide lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ≥ 65 years or ineligible for high dose chemotherapy. thalidomide lipomed is prescribed and dispensed in accordance with the thalidomide lipomed pregnancy prevention programme (see section 4.

Europska Unija - hrvatski - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - multipli mijelom - antineoplastična sredstva - tecvayli is indicated as monotherapy 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.

Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

galenika d.o.o. - bortezomib - prašak za rastvor za injekciju - 3,5 mg/1 bočica - 1 bočica praška za rastvor za injekciju sadrži: bortezomiba 3,5 mg

Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

pharmas d.o.o. sarajevo - bortezomib - prašak za otopinu za injekciju - 3,5 mg/1 bočica - 1 bočica sadrži: 3,5 mg bortezomiba (u obliku estra boronatne kiseline i manitola).

Europska Unija - hrvatski - EMA (European Medicines Agency)

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - Иммуностимуляторы, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

onkogen kft., becsi ut 77-79, budimpešta, mađarska - pleriksafor - otopina za injekciju - urbroj: 1 ml otopine sadrži 20 mg pleriksafora jedna bočica sadrži 24 mg pleriksafora u 1,2 ml otopine