MabCampath European Union - English - EMA (European Medicines Agency)

mabcampath

genzyme europe b.v. - alemtuzumab - leukemia, lymphocytic, chronic, b-cell - antineoplastic agents - mabcampath is indicated for the treatment of patients with b-cell chronic lymphocytic leukaemia (bcll) for whom fludarabine combination chemotherapy is not appropriate.

Tasermity European Union - English - EMA (European Medicines Agency)

tasermity

genzyme europe bv - sevelamer hydrochloride - hyperphosphatemia; renal dialysis - all other therapeutic products - tasermity is indicated for the control of hyperphosphataemia in adult patients receiving haemodialysis or peritoneal dialysis. sevelamer hydrochloride should be used within the context of a multiple therapeutic approach, which could include calcium supplements, 1,25 dihydroxy vitamin d3 or one of its analogues to control the development of renal bone disease.,

Fludara 50 mg powder for solution for injection or infusion Ireland - English - HPRA (Health Products Regulatory Authority)

fludara 50 mg powder for solution for injection or infusion

genzyme europe b.v. - fludarabine phosphate - powder for solution for injection/infusion - 50 milligram(s) - purine analogues; fludarabine

Fludara  50mg Powder for Solution for Injection or Infusion Malta - English - Medicines Authority

fludara 50mg powder for solution for injection or infusion

genzyme europe bv paasheuvelweg 25, 1105 bp amsterdam , netherlands - fludarabine phosphate - powder for solution for infusion or injection - fludarabine phosphate 25 mg/ml - antineoplastic agents

Fludara oral 10mg film-coated Tablets Malta - English - Medicines Authority

fludara oral 10mg film-coated tablets

genzyme europe bv paasheuvelweg 25, 1105 bp amsterdam , netherlands - fludarabine phosphate - film-coated tablet - fludarabine phosphate 10 mg - antineoplastic agents

Lemtrada 12 mg concentrate for solution for infusion European Union - English - myHealthbox

lemtrada 12 mg concentrate for solution for infusion

genzyme therapeutics ltd - alemtuzumab - concentrate for solution for infusion - 12 mg alemtuzumab in 1.2 ml (10 mg/ml) - multiple sclerosis - selective immunosuppressants - indicated for adult patients with relapsing remitting multiple sclerosis (rrms) with active disease defined by clinical or imaging features