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

mvabea

janssen-cilag international n.v.    - recombinant modified vaccinia ankara bavarian nordic virus encoding the: ebola virus zaire (zebov) mayinga strain glycoprotein (gp); ebola virus sudan gulu strain gp; ebola virus taï forest strain nucleoprotein and the marburg virus musoke strain gp - la fiebre hemorrágica, el Ébola - vacunas - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

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

imvanex

bavarian nordic a/s - vacuna modificada ankara - virus nórdico bávaro (mva-bn) - smallpox vaccine; monkeypox virus - otras vacunas virales, - active immunisation against smallpox, monkeypox and disease caused by vaccinia virus in adults (see sections 4. 4 y 5. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

VIVOTIF CAPSULAS DURAS GASTRORRESISTENTES España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

vivotif capsulas duras gastrorresistentes

bavarian nordic a/s - salmonella typhi cepa ty-21a,germenes vivos - cÁpsula dura gastrorresistente - n/a (vacuna) - salmonella typhi cepa ty-21a,germenes vivos n/a (vacuna) n/a (vacuna) - tifoidea, viva atenuada, oral

RABIPUR POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE EN JERINGA PRECARGADA España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

rabipur polvo y disolvente para solucion inyectable en jeringa precargada

bavarian nordic a/s - virus rabia inactivado - polvo y disolvente para soluciÓn inyectable en jeringa precargada - n/a (vacuna) - virus rabia inactivado n/a (vacuna) n/a (más de 4 pa) - rabia, virus entero inactivado

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

vaxchora

bavarian nordic a/s - vibrio cholerae, la cepa de cvd 103-hgr, vivir - cólera - vacunas - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. esta vacuna debe ser utilizado de acuerdo con las recomendaciones oficiales.

Heplisav B Unión Europea - español - EMA (European Medicines Agency)

heplisav b

dynavax gmbh - antígeno de superfície para la hepatitis b - hepatitis b - vacunas - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

Nobilis IB 4-91 Unión Europea - español - EMA (European Medicines Agency)

nobilis ib 4-91

intervet international bv - variante del virus de la bronquitis infecciosa aviar atenuada aviar cepa 4-91 - inmunológicos para aves - pollo - inmunización activa de pollos para reducir los signos respiratorios de la bronquitis infecciosa causada por la cepa variante ib 4-91.

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

oyavas

stada arzneimittel ag - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agentes antineoplásicos - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. para obtener más información sobre el estado del receptor 2 del factor de crecimiento epidérmico humano (her2), consulte la sección 5. oyavas in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with oyavas in combination with capecitabine. para más información sobre el estado de her2, consulte la sección 5. oyavas, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. oyavas, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. oyavas, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.