Unión Europea - español - EMA (European Medicines Agency)

inceptua ab - ocriplasmina - enfermedades de la retina - oftalmológicos - jetrea está indicado en adultos para el tratamiento de la tracción vitreomacular (vmt), incluso cuando se asocia con un agujero macular de diámetro inferior o igual a 400 micras.

Unión Europea - español - EMA (European Medicines Agency)

inceptua ab - paclitaxel - neoplasmas ováricos - antineoplastic agents, taxanes - apealea en combinación con carboplatino está indicado para el tratamiento de pacientes adultos con primera recaída de platino‑sensible cáncer epitelial de ovario, el cáncer peritoneal primario y el cáncer de las trompas de falopio.

Unión Europea - español - EMA (European Medicines Agency)

oncopeptides ab - melphalan flufenamide hydrochloride - mieloma múltiple - agentes antineoplásicos - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Unión Europea - español - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - palifermin - mucositis - todos los demás productos terapéuticos - kepivance está indicado para disminuir la incidencia, duración y severidad de la mucositis oral en pacientes adultos con neoplasias hematológicas recibir radiochemotherapy mieloablativo asociado a una alta incidencia de mucositis severo y que requieren apoyo autólogo-hematopoyéticas-células madre.

Unión Europea - español - EMA (European Medicines Agency)

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.

Unión Europea - español - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - agentes antineoplásicos - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Unión Europea - español - EMA (European Medicines Agency)

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.

Unión Europea - español - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - inmunosupresores - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Unión Europea - español - EMA (European Medicines Agency)

astrazeneca ab - virus de la gripe reagrupado (vivo atenuado) de la siguiente cepa: cepa a / vietnam / 1203/2004 (h5n1) - influenza, humano - vacunas - profilaxis de la influenza en una situación de pandemia declarada oficialmente en niños y adolescentes de 12 meses a menos de 18 años de edad. vacuna contra la influenza pandémica h5n1 astrazeneca debe ser utilizado de acuerdo con las directrices oficiales.

Guatemala - español - Gobierno de Guatemala, Ministerio de Salud Pública y Asistencia Social (Departamento de Regulación y Control de Productos Farmacéuticos y Afines)

pharmakon, s.a, - solución oral - 120 mg/5ml