Unión Europea - español - EMA (European Medicines Agency)

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - el dengue - vacunas - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 y 4. el uso de dengvaxia debe estar en conformidad con las recomendaciones oficiales.

Unión Europea - español - EMA (European Medicines Agency)

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - inmunológicos para suidos - los cerdos (de engorde) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Unión Europea - español - EMA (European Medicines Agency)

zoetis belgium sa - inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2 orf2 protein, inactivated mycoplasma hyopneumoniae, strain p-5722-3 - inactivado virales y bacterianas inactivadas vacunas - cerdos - para la inmunización activa de cerdos desde las 3 semanas de edad contra el circovirus porcino tipo 2 (pcv2) para reducir la carga viral en sangre y tejidos linfoides y la excreción fecal causada por la infección con pcv2. para la inmunización activa de cerdos mayores de 3 semanas contra mycoplasma hyopneumoniae para reducir las lesiones pulmonares causadas por la infección con m. hyopneumoniae.

Unión Europea - español - EMA (European Medicines Agency)

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) - linfoma, célula del manto - agentes antineoplásicos - 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).

Unión Europea - español - EMA (European Medicines Agency)

fresenius kabi deutschland gmbh - tocilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - inmunosupresores - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

arkopharma, s.a. - hypericum perforatum exto seco - cÁpsula dura - 175 mg - hypericum perforatum exto seco 175 mg - otros antidepresivos

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

uriach aquilea otc, s.l. - hypericum perforatum exto seco - excipientes: lactosa,carboximetilalmidon sodico - psicoestimulantes, agentes utilizados para la adhd y nootrÓpicos - otros psicoestimulantes y nootrópicos -

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

natysal, s.a. - hypericum perforatum - excipientes: croscarmelosa sodica,lactosa,jarabe de glucosa deshidratado,almidon de maiz - psicoestimulantes, agentes utilizados para la adhd y nootrÓpicos - otros psicoestimulantes y nootrópicos -

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

pan quimica-farmaceutica, s.a. - hypericum perforatum - excipientes: - antidepresivos - otros antidepresivos -

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

arkopharma, s.a. - hypericum perforatum exto seco - cÁpsula dura - 185 mg - hypericum perforatum exto seco 185 mg - otros psicoestimulantes y nootrópicos