Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - technetium (99m-tc) macrosalb - radiofarmaceutisk præparationssæt

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - betiatide - radiofarmaceutisk præparationssæt

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - technetium (99m-tc) pyrophosphat, tetranatriumpyrofosfatdecahydrat - radiofarmaceutisk præparationssæt

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - thallium (201-tl) chlorid - injektionsvæske, opløsning

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - tin(ii)chlorid (vandfri) - radiofarmaceutisk præparationssæt

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

curium netherlands b.v. - natriumpertechnetat (99m-tc) - radionuklidgenerator

Den Europæiske Union - dansk - EMA (European Medicines Agency)

serb sa - amifampridine phosphate - lambert-eaton myasthenic syndrome; paraneoplastic syndromes, nervous system; nervous system neoplasms; paraneoplastic syndromes; nervous system diseases; autoimmune diseases of the nervous system; neurodegenerative diseases; neuromuscular diseases; neuromuscular junction diseases; immune system diseases; autoimmune diseases; autoimmune diseases of the nervous system; cancer; neoplasms - andre narkotika stoffer - symptomatisk behandling af lambert-eaton myasthenisk syndrom (lems) hos voksne.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

aspen pharma trading limited - adrenalintartrat, lidocainhydrochlorid, vandfrit - injektionsvæske, opløsning - 10 mg/ml+5 mikrog/ml

Den Europæiske Union - dansk - EMA (European Medicines Agency)

accord healthcare s.l.u. - dexmedetomidin - præmedicinering - psykoleptika - til sedering af voksne intensiv afdeling (intensiv afdeling) patienter, der kræver en sedation niveau, der ikke er dybere end ophidselse i respons på verbal stimulation (svarende til richmond agitation-sedation scale (rass) 0 til -3). til sedering af ikke-intuberet voksne patienter før og/eller under diagnostiske og kirurgiske procedurer, som kræver, sedation, jeg. proceduremæssige/vågen sedation.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - graft afvisning - immunosuppressiva - 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.