Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abbvie a/s - sevofluranum inn - innöndunargufa, gegndreyptur stabbi - 100 %

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

baxter medical ab* - sevofluranum inn - innöndunargufa, gegndreyptur stabbi - 100 %

Evrópusambandið - íslenska - EMA (European Medicines Agency)

orion corporation - dexmedetomidine hydrochloride - meðvitandi sedation - psycholeptics - til róandi fullorðinsþjálfunaraðila sem krefjast róandi stigs ekki dýpra en vökva sem svar við munnlegri örvun (samsvarandi richmond agitation-sedation scale (rass) 0 til -3).

Evrópusambandið - íslenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - dexmedetomidine - lyfjaforgjöf - psycholeptics - fyrir róandi fullorðinna gjÖrgÆslu (gjörgæsludeild) sjúklingar sem krefjast róandi stigi ekki dýpra en örvun til að bregðast við munnleg örvun (svarar til richmond Æsingur-róandi mælikvarða (rass) 0 að -3). fyrir róandi ekki með leiðslur fullorðinn sjúklinga áður og/eða á greiningu eða skurðaðgerðir þurfa róandi, ég. málsmeðferð/vakandi róandi.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - graft rejection - Ónæmisbælandi lyf - 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.

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

piramal critical care b.v. - sevofluranum inn - innöndunargufa, gegndreyptur stabbi - 100 %

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fresenius kabi ab - propofolum inn - stungulyf/innrennslislyf, fleyti - 10 mg/ml

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

krka sverige ab - sertralinum hýdróklóríð - filmuhúðuð tafla - 100 mg

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

baxter medical ab* - desfluranum inn - innöndunargufa, gegndreyptur stabbi

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

bluefish pharmaceuticals ab - sertralinum hýdróklóríð - filmuhúðuð tafla - 50 mg