Daxas Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

daxas

astrazeneca ab - roflumilast - enfermedad pulmonar, obstructiva crónica - medicamentos para la enfermedad obstructiva de las vías respiratorias enfermedades, - daxas está indicado para el tratamiento de mantenimiento de severa enfermedad pulmonar obstructiva crónica (epoc) (fev1 post-broncodilatador inferior al 50% predicho) asociada a bronquitis crónica en pacientes adultos con un historial de exacerbaciones frecuentes como complemento a tratamiento broncodilatador.

Faslodex Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

faslodex

astrazeneca ab - fulvestrant - neoplasias de la mama - la terapia endocrina, anti-estrógenos - faslodex is indicated , as monotherapy for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women:, , not previously treated with endocrine therapy, or, with disease relapse on or after adjuvant antiestrogen therapy, or disease progression on antiestrogen therapy. , , , in combination with palbociclib for the treatment of hormone receptor (hr)-positive, human epidermal growth factor receptor 2 (her2)-negative locally advanced or metastatic breast cancer in women who have received prior endocrine therapy. en pre - o cerca de la menopausia de las mujeres, el tratamiento de combinación con palbociclib debe ser combinado con una hormona liberadora de hormona luteinizante (lhrh) agonista.

Tagrisso Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

tagrisso

astrazeneca ab - osimertinib mesilate - carcinoma, pulmón no microcítico - otros agentes antineoplásicos, inhibidores de la proteína quinasa - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Xigduo Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

xigduo

astrazeneca ab - metformina clorhidrato, dapaglifozina propanodiol monohidrato - diabetes mellitus, tipo 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - xigduo está indicado en adultos para el tratamiento de la diabetes mellitus tipo 2 como un complemento a la dieta y el ejercicio:• en pacientes insuficientemente controlados en su dosis máxima tolerada de metformina sola • en combinación con otros medicamentos para el tratamiento de la diabetes en pacientes insuficientemente controlados con metformina y estos productos medicinales• en los pacientes que ya estén siendo tratados con la combinación de dapagliflozin and metformin como independiente tabletas. para que los resultados del estudio con respecto a la combinación de las terapias, los efectos sobre el control glucémico y los eventos cardiovasculares, y las poblaciones estudiadas, ver las secciones 4. 4, 4. 5 y 5.

Ondexxya Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

ondexxya

astrazeneca ab - andexanet alfa - relacionados con drogas efectos secundarios y reacciones adversas - todos los demás productos terapéuticos - para los pacientes adultos tratados con un directo del factor xa (fxa) inhibidor (apixaban o rivaroxaban) cuando la reversión de la anticoagulación es necesaria debido a que amenaza la vida o sangrado incontrolable.

Trixeo Aerosphere Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

trixeo aerosphere

astrazeneca ab - formoterol fumarate dihydrate, glycopyrronium bromide, budesonide - enfermedad pulmonar, obstructiva crónica - medicamentos para la enfermedad obstructiva de las vías respiratorias enfermedades, - trixeo aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long acting beta2 agonist or combination of a long-acting beta2 agonist and a long acting muscarinic antagonist.

Calquence Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

calquence

astrazeneca ab - acalabrutinib - leucemia, linfocítica, crónica, b-cell - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Lumoxiti Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

lumoxiti

astrazeneca ab - moxetumomab pasudotox - leucemia, hairy cell - agentes antineoplásicos - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Evusheld Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

Saphnelo Kesatuan Eropah - Sepanyol - EMA (European Medicines Agency)

saphnelo

astrazeneca ab - anifrolumab - lupus eritematoso, sistémico - inmunosupresores - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.