IMMUNOPRIN 75 MG õhukese polümeerikattega tablett أستونيا - الإستونية - Ravimiamet

immunoprin 75 mg õhukese polümeerikattega tablett

sandoz pharmaceuticals d.d. - asatiopriin - õhukese polümeerikattega tablett - 75mg 50tk

IMMUNOPRIN 100 MG õhukese polümeerikattega tablett أستونيا - الإستونية - Ravimiamet

immunoprin 100 mg õhukese polümeerikattega tablett

sandoz pharmaceuticals d.d. - asatiopriin - õhukese polümeerikattega tablett - 100mg 100tk; 100mg 50tk

Jayempi الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - transplantaadi tagasilükkamine - immunosupressandid - 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.

Capecitabine SUN الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

capecitabine sun

sun pharmaceutical industries europe b.v. - kapetsitabiin - stomach neoplasms; breast neoplasms; colonic neoplasms; colorectal neoplasms - kapetsitabiin - kapetsitabiini on näidustatud käärsoolevähi adjuvantravina operatsiooni kasvaja iii staadium (dukes´i etapp-c). capecitabine on näidustatud ravi metastaatilise kolorektaalse vähi. capecitabine on näidustatud esimese rea ravi arenenud mao-vähi koos plaatina baasil raviskeemi. capecitabine koos docetaxel on näidustatud ravi patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise rinnavähi pärast rikke tsütotoksilist keemiaravi. eelnev ravi peaks sisaldama antratsükliini. capecitabine on ka märgitud, et monotherapy raviks patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise rinnavähi pärast rikke taxanes ja anthracycline-sisaldava keemiaravi raviskeemi või kelle jaoks veelgi anthracycline ravi ei ole näidustatud.

Lemtrada الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

lemtrada

sanofi belgium - alemtuzumab - hulgiskleroos - selektiivsed immunosupressandid - lemtrada on näidustatud kliiniliste või pildistamisfunktsioonidega määratletud aktiivse haigusega täiskasvanud patsientidel, kellel on retsidiveeruvat remissiooni hulgiskleroos (rrms).

Thalidomide BMS (previously Thalidomide Celgene) الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

thalidomide bms (previously thalidomide celgene)

bristol-myers squibb pharma eeig - talidomiid - mitu müeloomit - immunosupressandid - thalidomide bms in combination with melphalan and prednisone as first line treatment of patients with untreated multiple myeloma, aged >/= 65 years or ineligible for high dose chemotherapy. thalidomide bms is prescribed and dispensed according to the thalidomide celgene pregnancy prevention programme (see section 4.

Verkazia الاتحاد الأوروبي - الإستونية - EMA (European Medicines Agency)

verkazia

santen oy - tsüklosporiin - conjunctivitis; keratitis - oftalmoloogilised vahendid - ravi raskeid kevadine keratoconjunctivitis (vkc) lastele alates 4 aasta vanusest ja noorukid.

METHOTREXATE ACCORD süstelahus أستونيا - الإستونية - Ravimiamet

methotrexate accord süstelahus

accord healthcare b.v. - metotreksaat - süstelahus - 25mg 1ml 20ml 1tk; 25mg 1ml 40ml 10tk; 25mg 1ml 20ml 10tk; 25mg 1ml 2ml 1tk

VARIVAX süstesuspensiooni pulber ja lahusti süstlis أستونيا - الإستونية - Ravimiamet

varivax süstesuspensiooni pulber ja lahusti süstlis

merck sharp & dohme b.v. - tuulerõugete viirus, elus, nõrgestatud - süstesuspensiooni pulber ja lahusti süstlis - 1annus 0.5ml 0.5ml 1tk; 0.5ml 10tk; 0.5ml 1tk

INZOLFI kõvakapsel أستونيا - الإستونية - Ravimiamet

inzolfi kõvakapsel

sandoz pharmaceuticals d.d. - fingolimood - kõvakapsel - 0,25mg 28tk