torisel 30 mg/1 bočica koncentrat i razrjeđivač za otopinu za infuziju
pfizer bh d.o.o. sarajevo - temsirolimus - koncentrat i razrjeđivač za otopinu za infuziju - 30 mg/1 bočica - 1 bočica sa 1,2 ml koncentrata za otopinu za infuziju sadrži: 30 mg temsirolimusa
rapamune
pfizer europe ma eeig - sirolimus - graft rejection; kidney transplantation - imunosupresivi - zdravilo rapamune je indicirano za profilakso zavrnitve organa pri odraslih bolnikih z majhnim do zmernim imunskim tveganjem, ki prejemajo presaditev ledvic. priporočljivo je, da rapamune uporablja sprva v kombinaciji z ciclosporin microemulsion in kortikosteroidi za 2 do 3 mesece. rapamune lahko nadaljeval, kot vzdrževalna terapija s kortikosteroidi le, če ciclosporin microemulsion lahko postopno opuščeni. rapamune je indiciran za zdravljenje bolnikov z občasno lymphangioleiomyomatosis z zmerno boleznijo pljuč ali upada pljučne funkcije.
斥消靈錠 2 毫克
美商惠氏藥廠(亞洲)股份有限公司台灣分公司 台北市信義區松仁路100號42、43樓 (23984410) - sirolimus nanosystems dispersion - 糖衣錠 - 主成分 (active filler coat:) ; sirolimus nanosystems dispersion (9200039620) sirolimus 100% 2mg,poloxamer 188 1 mgmg - sirolimus - 1.與cyclosporine及皮質類固醇合併使用來預防病人腎臟移植後之器官排斥。2.若病人有低度或中度免疫上的危險於移植後2到4個月,可以逐步停止使用cyclosporine而斥消靈 (sirolimus)應增加劑量至到達血中建議濃度。
斥消靈錠1毫克
美商惠氏藥廠(亞洲)股份有限公司台灣分公司 台北市信義區松仁路100號42、43樓 (23984410) - sirolimus nanosystems dispersion;;sirolimus - 糖衣錠 - 主成分 (active filler coat:) ; sirolimus nanosystems dispersion (9200039620) (150mg/g)mg; sirolimus (9200039600) 100%mg - sirolimus - 1、適用於與cyclosporine及皮質類固醇合併使用來預防病人腎臟移植後之器官排斥。2、適用於淋巴血管平滑肌增生症(lymphangioleiomyomatosis,簡稱lam)成人病人的治療。
torisel
pfizer europe ma eeig - temsirolimus - carcinoma, renal cell; lymphoma, mantle-cell - antineoplastic agents - renal-cell carcinomatorisel is indicated for the first-line treatment of adult patients with advanced renal-cell carcinoma (rcc) who have at least three of six prognostic risk factors.mantle-cell lymphomatorisel is indicated for the treatment of adult patients with relapsed and / or refractory mantle-cell lymphoma (mcl).
rapamune
pfizer new zealand limited - sirolimus 1 mg/ml; - oral solution - 1 mg/ml - active: sirolimus 1 mg/ml excipient: phosal 50 pg polysorbate 80 - rapamune is indicated for the prophylaxis of organ rejection in patients at mild to moderate immunological risk receiving renal transplants. therapeutic drug monitoring of sirolimus is required.
hyftor
plusultra pharma gmbh - sirolimus - angiofibroma; tuberous sclerosis - hyftor is indicated for the treatment of facial angiofibroma associated with tuberous sclerosis complex in adults and paediatric patients aged 6 years and older.
temsirolimus accord 30 mg koncentrátum és oldószer oldatos infúzióhoz
accord healthcare polska sp. z o.o. - temszirolimusszal -
rapamune 1 mg/ml soluzione orale
pfizer ag - sirolimusum - soluzione orale - sirolimusum 1 mg, polysorbatum 80, phosphatidylcholinum, sojae olio 20 mg, mono/diglycerida, ethanolum il 96 per cento 20 mg, propylenglycolum 350 mg, e 304, per la soluzione 1 ml, ethanolum 3.17 % v/v. - immunsuppressivum - biotechnologika
rapamune 1 mg compresse rivestite
pfizer ag - sirolimusum - compresse rivestite - sirolimusum 1 mg, poloxamerum 188, lactosum monohydricum 86.4 mg, macrogolum 8000, magnesio stearas, talco, macrogolum 20'000, glyceroli mono-oleas, lacca, calcio sulfas anhydricus, cellulosum microcristallinum, sintetico 213.85 mg, e 171, povidonum k 29-32, int-rac-alfa-tocopherylis acetas, cera carnauba, drucktinte: lacca, e 172 (rosso), propylenglycolum, simeticonum, per compresso haze. - immunsuppressivum - biotechnologika