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

nyxoid

mundipharma corporation (ireland) limited - la naloxona clorhidrato dihidratado - trastornos relacionados con los opioides - todos los demás productos terapéuticos - nyxoid está pensado para la administración inmediata como tratamiento de emergencia para la sobredosis de opiáceos o sospechada como se manifiesta por depresión del sistema nervioso central y respiratoria en contextos no médicos y de salud. nyxoid is indicated in adults and adolescents aged 14 years and over. nyxoid is not a substitute for emergency medical care.

Flebogamma DIF (previously Flebogammadif) Unión Europea - español - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - la inmunoglobulina humana normal - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - los sueros inmunes e inmunoglobulinas, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

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

jayempi

nova laboratories ireland limited - azathioprine - rechazo del injerto - inmunosupresores - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

ALIKAL UNIDAD 2 - COMPRIMIDOS Argentina - español - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

alikal unidad 2 - comprimidos

glaxosmithkline argentina s.a. - acido acetil salicilico - comprimidos - acido acetilsalicilico 0.48 g; cafeina anhidra 0.05 g

ALIKAL- SABOR NARANJA - POLVO Argentina - español - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

alikal- sabor naranja - polvo

glaxosmithkline argentina s.a. - acido citrico - polvo efervescente - acido citrico 43.100 g; carbonato de sodio 10 g

ALIKAL- SABOR NARANJA - POLVO Argentina - español - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

alikal- sabor naranja - polvo

glaxosmithkline argentina s.a. - acido citrico - polvo efervescente - acido citrico 43.100 g; carbonato de sodio 10 g