Felpreva Европейски съюз - български - EMA (European Medicines Agency)

felpreva

vétoquinol sa - emodepside, praziquantel, tigolaner - Антгельминтики, - Котки - for cats with, or at risk from, mixed parasitic infestations. the veterinary medicinal product is exclusively indicated when ectoparasites, cestodes and nematodes are targeted at the same time.

Eurartesim Европейски съюз - български - EMA (European Medicines Agency)

eurartesim

alfasigma s.p.a. - piperaquine tetraphosphate, artenimol - малария - антипротозойни - eurartesim е показан за лечение на неусложнена малария plasmodium falciparum при възрастни, деца и бебета на 6 месеца и повече и с тегло 5 kg или повече. Трябва да се вземат предвид официалните препоръки за правилното използване на малария агенти.

Okedi Европейски съюз - български - EMA (European Medicines Agency)

okedi

laboratorios farmacéuticos rovi, s.a. - Рисперидон - шизофрения - психолептици - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

Vectra Felis Европейски съюз - български - EMA (European Medicines Agency)

vectra felis

ceva santé animale - pyriproxyfen, dinotefuran - Антипаразитни препарати, инсектициди и репеленти, други ectoparasiticides за външно приложение, pyriproxyfen, комбинации - Котки - Лечение и профилактика на инвазия на бълхи (ctenocephalides Фелиз) на котки. Едно приложение предотвратява бълха паразитози в рамките на един месец. Той също така пречи на размножаването на бълхите, предотвратява появата на бълхите в околната среда на котката, на 3 месеца.

Abecma Европейски съюз - български - 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 - Антинеопластични средства - 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 Европейски съюз - български - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - Множествена миелома - 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.

Tecartus Европейски съюз - български - EMA (European Medicines Agency)

tecartus

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - Лимфом, мантел-клетка - Антинеопластични средства - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Ebvallo Европейски съюз - български - EMA (European Medicines Agency)

ebvallo

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.