Arepanrix Unión Europea - español - EMA (European Medicines Agency)

arepanrix

glaxosmithkline biologicals s.a. - división de virus de influenza inactivados, que contienen el antígeno*: a/california/7/2009 (h1n1)v como tensión (x-179 bis)*propagado en huevos. - influenza, human; immunization; disease outbreaks - vacunas contra la gripe - profilaxis de la influenza en una situación de pandemia oficialmente declarada. la vacuna contra la influenza pandémica debe usarse de acuerdo con la guía oficial.

Prepandemic Influenza Vaccine (H5N1) (Split Virion, Inactivated, Adjuvanted) GlaxoSmithKline Biologicals Unión Europea - español - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals

glaxosmithkline biologicals s.a. - virus de la gripe dividido, inactivado, que contiene el antígeno: a / vietnam / 1194/2004 (h5n1) como la cepa utilizada (nibrg-14) - influenza, human; immunization; disease outbreaks - vacunas - inmunización activa contra el subtipo h5n1 del virus influenza a. esta indicación se basa en la inmunogenicidad de datos de sujetos sanos a partir de la edad de 18 años en adelante tras la administración de dos dosis de la vacuna preparada a partir de a/vietnam/1194/2004 nibrg-14 (h5n1) (véase la sección 5. prepandémico influenza vaccine (h5n1) (split virión, inactivado, con adyuvante) de glaxosmithkline biologicals 3. 75 µg debe ser utilizado de acuerdo con las directrices oficiales.

KOATE DVI Argentina - español - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

koate dvi

tuteur s.a.c.i.f.i.a. - factor antihemofilico humano - inyectable - factor antihemofilico humano 1000 ui / frasco ampolla

KOATE DVI Argentina - español - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

koate dvi

tuteur s.a.c.i.f.i.a. - factor antihemofilico humano - inyectable - factor antihemofilico humano 500 ui / frasco ampolla

Doptelet Unión Europea - español - EMA (European Medicines Agency)

doptelet

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocitopenia - antihemorrágicos - doptelet está indicado para el tratamiento de la trombocitopenia severa en pacientes adultos con enfermedad hepática crónica que está programado para someterse a un procedimiento invasivo. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. corticosteroides, inmunoglobulinas).

Abecma Unión Europea - español - 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 - agentes antineoplásicos - 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.

Enjaymo Unión Europea - español - EMA (European Medicines Agency)

enjaymo

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - inmunosupresores - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Tevimbra Unión Europea - español - EMA (European Medicines Agency)

tevimbra

novartis europharm limited - tislelizumab - esophageal squamous cell carcinoma - agentes antineoplásicos - oesophageal squamous cell carcinoma (oscc) tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic oesophageal squamous cell carcinoma after prior platinum-based chemotherapy.

Fluenz Tetra Unión Europea - español - EMA (European Medicines Agency)

fluenz tetra

astrazeneca ab - a/darwin/9/2021 (h3n2) - like strain (a/norway/16606/2021, medi 355293) / a/victoria/2570/2019 (h1n1)pdm09 - like strain (a/victoria/1/2020, medi 340505) / b/austria/1359417/2021 - like strain (b/austria/1359417/2021, medi 355292) / b/phuket/3073/2013 - like strain (b/phuket/3073/2013, medi 306444) - influenza, humano - las vacunas contra la gripe, la gripe, el virus vivos atenuados - prophylaxis of influenza in children and adolescents from 24 months to less than 18 years of age. el uso de fluenz tetra debe basarse en las recomendaciones oficiales.

Zolsketil pegylated liposomal Unión Europea - español - EMA (European Medicines Agency)

zolsketil pegylated liposomal

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.