Sehcat 370 kBq Kapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sehcat 370 kbq kapsel, hård

ge healthcare buchler gmbh & co. kg - tauroselcholsyra (se-75) - kapsel, hård - 370 kbq - tauroselcholsyra (se-75) 370 kbq aktiv substans - selenium(se-75)tauroselcholsyra

Jayempi Europeiska unionen - svenska - EMA (European Medicines Agency)

jayempi

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.

Otezla Europeiska unionen - svenska - EMA (European Medicines Agency)

otezla

amgen europe bv - apremilast - arthritis, psoriatic; psoriasis - immunsuppressiva - psoriasisartrit arthritisotezla, ensamt eller i kombination med sjukdomsmodifierande antireumatiska läkemedel (dmard), är indicerat för behandling av aktiv psoriasisartrit (psa) hos vuxna patienter som har haft ett otillräckligt svar eller som har varit intoleranta mot en tidigare dmard behandling. psoriasisotezla är indicerat för behandling av måttlig till svår kronisk plackpsoriasis hos vuxna patienter som inte svarat på eller som har en kontraindikation mot, eller som är intoleranta mot annan systemisk behandling, inklusive ciklosporin, metotrexat eller psoralen och uv-ljus (puva).

Ciprofloxacin MDS 250 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciprofloxacin mds 250 mg filmdragerad tablett

medical drug supplies ltd - ciprofloxacinhydroklorid (monohydrat) - filmdragerad tablett - 250 mg - ciprofloxacinhydroklorid (monohydrat) 291,1 mg aktiv substans; laktosmonohydrat hjälpämne - ciprofloxacin

Ciprofloxacin MDS 500 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciprofloxacin mds 500 mg filmdragerad tablett

medical drug supplies ltd - ciprofloxacinhydroklorid (monohydrat) - filmdragerad tablett - 500 mg - ciprofloxacinhydroklorid (monohydrat) 582,2 mg aktiv substans; laktosmonohydrat hjälpämne - ciprofloxacin

Ciprofloxacin MDS 750 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciprofloxacin mds 750 mg filmdragerad tablett

medical drug supplies ltd - ciprofloxacinhydroklorid (monohydrat) - filmdragerad tablett - 750 mg - ciprofloxacinhydroklorid (monohydrat) 873,3 mg aktiv substans; laktosmonohydrat hjälpämne - ciprofloxacin

Ciprofloxacin Accord 500 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciprofloxacin accord 500 mg filmdragerad tablett

ebb medical ab - ciprofloxacinhydroklorid (monohydrat) - filmdragerad tablett - 500 mg - laktosmonohydrat hjälpämne; ciprofloxacinhydroklorid (monohydrat) 582,2 mg aktiv substans

Ciprofloxacin Accord 250 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciprofloxacin accord 250 mg filmdragerad tablett

ebb medical ab - ciprofloxacinhydroklorid (monohydrat) - filmdragerad tablett - 250 mg - ciprofloxacinhydroklorid (monohydrat) 291,1 mg aktiv substans; laktosmonohydrat hjälpämne

Sandimmun Neoral 10 mg Kapsel, mjuk Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandimmun neoral 10 mg kapsel, mjuk

novartis sverige ab - ciklosporin - kapsel, mjuk - 10 mg - ciklosporin 10 mg aktiv substans; propylenglykol hjälpämne; glycerol 85% hjälpämne; makrogolglycerolhydroxistearat hjälpämne; etanol, vattenfri hjälpämne - ciklosporin

Ciqorin 10 mg Kapsel, mjuk Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ciqorin 10 mg kapsel, mjuk

teva sweden ab - ciklosporin - kapsel, mjuk - 10 mg - etanol, vattenfri hjälpämne; ciklosporin 10 mg aktiv substans; makrogolglycerolhydroxistearat hjälpämne; glycerol 85% hjälpämne; sorbitol hjälpämne - ciklosporin