Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ethypharm sa - suxametoniumklorid (dihydrat) - injektions-/infusionsvätska, lösning - 50 mg/ml - suxametoniumklorid (dihydrat) 50 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

laboratoire aguettant - suxametoniumklorid (vattenfri) - injektionsvätska, lösning i förfylld spruta - 10 mg/ml - suxametoniumklorid (vattenfri) 10 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

panpharma sa - suxametoniumklorid (dihydrat) - injektions-/infusionsvätska, lösning - 50 mg/ml - suxametoniumklorid (dihydrat) 55 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

viatris ab - suxametoniumklorid (dihydrat) - injektionsvätska, lösning - 50 mg/ml - suxametoniumklorid (dihydrat) 50 mg aktiv substans - suxameton

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius kabi ab - irinotekanhydrokloridtrihydrat - koncentrat till infusionsvätska, lösning - 20 mg/ml - sorbitol hjälpämne; irinotekanhydrokloridtrihydrat 20 mg aktiv substans - irinotekan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - irinotekanhydrokloridtrihydrat - koncentrat till infusionsvätska, lösning - 20 mg/ml - irinotekanhydrokloridtrihydrat 20 mg aktiv substans; sorbitol hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

abboxia ab - tiopentalnatrium - pulver till injektionsvätska, lösning - tiopentalnatrium 1 g aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - graftförkastning - immunsuppressiva - 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.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

carinopharm gmbh - metoprololtartrat - injektionsvätska, lösning - 1 mg/ml - metoprololtartrat 1 mg aktiv substans - metoprolol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

hexal a/s - paroxetinhydroklorid (vattenfri) - filmdragerad tablett - 10 mg - paroxetinhydroklorid (vattenfri) 11,1 mg aktiv substans; mannitol hjälpämne - paroxetin