JIVI damoctocog alfa pegol 2000 IU powder for injection vial with diluent syringe Australia - engelsk - Department of Health (Therapeutic Goods Administration)

jivi damoctocog alfa pegol 2000 iu powder for injection vial with diluent syringe

bayer australia ltd - damoctocog alfa pegol, quantity: 2000 iu - injection, powder for - excipient ingredients: glycine; histidine; sucrose; calcium chloride dihydrate; sodium chloride; polysorbate 80 - jivi, damoctocog alfa pegol, is a long-acting recombinant factor viii concentrate indicated for use in previously treated adults and adolescents (12 years of age and older) with haemophilia a for:,? routine prophylactic treatment to prevent or reduce the frequency of bleeding episodes,? on-demand treatment and control of bleeding episodes,? per-operative management of bleeding (surgical prophylaxis),jivi does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand?s disease.

JIVI damoctocog alfa pegol 1000 IU powder for injection vial with diluent syringe Australia - engelsk - Department of Health (Therapeutic Goods Administration)

jivi damoctocog alfa pegol 1000 iu powder for injection vial with diluent syringe

bayer australia ltd - damoctocog alfa pegol, quantity: 1000 iu - injection, powder for - excipient ingredients: polysorbate 80; calcium chloride dihydrate; glycine; sodium chloride; sucrose; histidine - jivi, damoctocog alfa pegol, is a long-acting recombinant factor viii concentrate indicated for use in previously treated adults and adolescents (12 years of age and older) with haemophilia a for:,? routine prophylactic treatment to prevent or reduce the frequency of bleeding episodes,? on-demand treatment and control of bleeding episodes,? per-operative management of bleeding (surgical prophylaxis),jivi does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand?s disease.

JIVI damoctocog alfa pegol 250 IU powder for injection vial with diluent syringe Australia - engelsk - Department of Health (Therapeutic Goods Administration)

jivi damoctocog alfa pegol 250 iu powder for injection vial with diluent syringe

bayer australia ltd - damoctocog alfa pegol, quantity: 250 iu - injection, powder for - excipient ingredients: polysorbate 80; sucrose; glycine; calcium chloride dihydrate; histidine; sodium chloride - jivi, damoctocog alfa pegol, is a long-acting recombinant factor viii concentrate indicated for use in previously treated adults and adolescents (12 years of age and older) with haemophilia a for:,? routine prophylactic treatment to prevent or reduce the frequency of bleeding episodes,? on-demand treatment and control of bleeding episodes,? per-operative management of bleeding (surgical prophylaxis),jivi does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand?s disease.

JIVI damoctocog alfa pegol 3000 IU powder for injection vial with diluent syringe Australia - engelsk - Department of Health (Therapeutic Goods Administration)

jivi damoctocog alfa pegol 3000 iu powder for injection vial with diluent syringe

bayer australia ltd - damoctocog alfa pegol, quantity: 3000 iu - injection, powder for - excipient ingredients: calcium chloride dihydrate; sucrose; sodium chloride; glycine; histidine; polysorbate 80 - jivi, damoctocog alfa pegol, is a long-acting recombinant factor viii concentrate indicated for use in previously treated adults and adolescents (12 years of age and older) with haemophilia a for:,? routine prophylactic treatment to prevent or reduce the frequency of bleeding episodes,? on-demand treatment and control of bleeding episodes,? per-operative management of bleeding (surgical prophylaxis),jivi does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand?s disease.

JIVI damoctocog alfa pegol 500 IU powder for injection vial with diluent syringe Australia - engelsk - Department of Health (Therapeutic Goods Administration)

jivi damoctocog alfa pegol 500 iu powder for injection vial with diluent syringe

bayer australia ltd - damoctocog alfa pegol, quantity: 500 iu - injection, powder for - excipient ingredients: sucrose; calcium chloride dihydrate; polysorbate 80; glycine; sodium chloride; histidine - jivi, damoctocog alfa pegol, is a long-acting recombinant factor viii concentrate indicated for use in previously treated adults and adolescents (12 years of age and older) with haemophilia a for:,? routine prophylactic treatment to prevent or reduce the frequency of bleeding episodes,? on-demand treatment and control of bleeding episodes,? per-operative management of bleeding (surgical prophylaxis),jivi does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand?s disease.

Jivi Den europeiske union - maltesisk - EMA (European Medicines Agency)

jivi

bayer ag - damoctocog alfa pegol - hemofilja a - sustanzi kontra l-emorraġija - kura u profilassi ta ' fsada f'pazjenti li kienu kkurati qabel ≥ 12-il sena bl-emofilja a (nuqqas konġenitali tal-fattur viii).

Jivi Den europeiske union - tsjekkisk - EMA (European Medicines Agency)

jivi

bayer ag - damoctocog alfa pegol - hemofilie a - antihemoragika - léčba a profylaxe krvácení u dříve léčených pacientů ve věku ≥ 12 let věku s hemofilií a (vrozený nedostatek faktoru viii).

Jivi Den europeiske union - dansk - EMA (European Medicines Agency)

jivi

bayer ag - damoctocog alfa pegol - hemophilia a - antihemorrhagics - behandling og profylakse af blødning hos tidligere behandlede patienter ≥ 12 år med hæmofili a (medfødt faktor viii-mangel).

Jivi Den europeiske union - tysk - EMA (European Medicines Agency)

jivi

bayer ag - damoctocog alfa pegol - hämophilie a - antihämorrhagika - behandlung und prophylaxe von blutungen bei zuvor behandelten patienten ≥ 12 jahren mit hämophilie a (angeborener faktor viii-mangel).

Jivi Den europeiske union - nederlandsk - EMA (European Medicines Agency)

jivi

bayer ag - damoctocog alfa pegol - hemophilia a - antihemorragica - behandeling en profylaxe van bloedingen in de eerder behandelde patiënten ≥ 12 jaar en ouder met hemofilie a (aangeboren factor viii-deficiëntie).