Tacforius Evrópusambandið - íslenska - EMA (European Medicines Agency)

tacforius

teva b.v. - takrólímus einhýdrat - liver transplantation; kidney transplantation - Ónæmisbælandi lyf - fyrirbyggja grætt höfnun í fullorðinn nýra eða lifur ígrædd nýru viðtakendur. meðferð við höfnun á fjölgildingu sem er ónæm fyrir meðferð með öðrum ónæmisbælandi lyfjum hjá fullorðnum sjúklingum.

Jayempi Evrópusambandið - íslenska - EMA (European Medicines Agency)

jayempi

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.

Amifampridine SERB Evrópusambandið - íslenska - EMA (European Medicines Agency)

amifampridine serb

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 - Önnur lyf í taugakerfinu - einkenni meðferðar á lambert-eaton vöðvaspennaheilkenni (lems) hjá fullorðnum.

Pemetrexed Baxter Evrópusambandið - íslenska - EMA (European Medicines Agency)

pemetrexed baxter

baxter holding b.v. - pemetrexed disodium heptahydrate - carcinoma, non-small-cell lung; mesothelioma - Æxlishemjandi lyf - malignant pleural mesotheliomapemetrexed baxter in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed baxter in combination with cisplatin is indicated for the first line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5. pemetrexed baxter is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy (see section 5. pemetrexed baxter is indicated as monotherapy for the second line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5.

Dailiport Hart forðahylki 5 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dailiport hart forðahylki 5 mg

sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 5 mg

Dailiport Hart forðahylki 0,5 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dailiport hart forðahylki 0,5 mg

sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 0,5 mg

Dailiport Hart forðahylki 1 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dailiport hart forðahylki 1 mg

sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 1 mg

Dailiport Hart forðahylki 2 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dailiport hart forðahylki 2 mg

sandoz a/s - tacrolimus; tacrolimus monohydrate - hart forðahylki - 2 mg

Dailiport Hart forðahylki 3 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dailiport hart forðahylki 3 mg

sandoz a/s - tacrolimus monohydrate; tacrolimus - hart forðahylki - 3 mg