ADVATE octocog alfa (rch) 250 IU powder for injection vial with diluent vial Australia - English - Department of Health (Therapeutic Goods Administration)

advate octocog alfa (rch) 250 iu powder for injection vial with diluent vial

takeda pharmaceuticals australia pty ltd - octocog alfa, quantity: 250 iu - diluent, not applicable - excipient ingredients: water for injections - advate is indicated for use in haemophilia a for prevention and control of harmorrhagic episodes. patients with haemophilia a may be treated with advate as perioperative management. advate is not indicated in von willebrand's disease.

ELOCTATE efmoroctocog alfa (rhu) 250 IU powder for injection vial and diluent pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

eloctate efmoroctocog alfa (rhu) 250 iu powder for injection vial and diluent pre-filled syringe

sanofi-aventis australia pty ltd - efmoroctocog alfa, quantity: 250 iu - drug delivery system - excipient ingredients: - eloctate is a long-acting antihaemophilic factor (recombinant) indicated in adults and children with haemophilia a (congenital factor viii deficiency) for: - control and prevention of bleeding episodes - routine prophylaxis to prevent or reduce the frequency of bleeding episodes - perioperative management (surgical prophylaxis). eloctate does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand's disease.

XYNTHA moroctocog alfa (rch) 250IU powder for injection vial and pre-filled diluent syringe Australia - English - Department of Health (Therapeutic Goods Administration)

xyntha moroctocog alfa (rch) 250iu powder for injection vial and pre-filled diluent syringe

pfizer australia pty ltd - moroctocog alfa, quantity: 250 iu - injection, powder for - excipient ingredients: polysorbate 80; sodium chloride; hydrochloric acid; histidine; sucrose; calcium chloride dihydrate - the control and prevention of haemorrhagic episodes in patients with haemophilia a, including control and prevention of bleeding in surgical settings. xyntha does not contain von willebrand factor and should not be used by patients with von willebrand's disease.

XYNTHA moroctocog alfa (rch) 250IU powder for injection and diluent dual-chamber syringe Australia - English - Department of Health (Therapeutic Goods Administration)

xyntha moroctocog alfa (rch) 250iu powder for injection and diluent dual-chamber syringe

pfizer australia pty ltd - moroctocog alfa, quantity: 250 iu - injection, solution - excipient ingredients: water for injections; sodium chloride - the control and prevention of haemorrhagic episodes in patients with haemophilia a, including control and prevention of bleeding in surgical settings. xyntha does not contain von willebrand factor and should not be used by patients with von willebrand's disease.

Recombinate 250 IU inj. sol. (pwdr. + solv.) i.v. vial Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

recombinate 250 iu inj. sol. (pwdr. + solv.) i.v. vial

baxalta innovations gmbh - octocog alfa 250 iu/5 ml - powder and solvent for solution for injection - 250 iu/ 5 ml - octocog alfa 250 iu - coagulation factor viii

Recombinate 250 IU/10 ml inj. sol. (pwdr. + solv.) i.v. vial Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

recombinate 250 iu/10 ml inj. sol. (pwdr. + solv.) i.v. vial

baxalta innovations gmbh - octocog alfa 250 iu/10 ml - powder and solvent for solution for injection - 250 iu/ 10 ml - octocog alfa 250 iu - coagulation factor viii

OBIZUR susoctocog alfa (bhk) 500U antihemophilic factor (recombinant), porcine sequence powder for injection vial with water for injection syringe Australia - English - Department of Health (Therapeutic Goods Administration)

obizur susoctocog alfa (bhk) 500u antihemophilic factor (recombinant), porcine sequence powder for injection vial with water for injection syringe

takeda pharmaceuticals australia pty ltd - susoctocog alfa, quantity: 500 u/ml - injection - excipient ingredients: - for the treatment of bleeding episodes in adults with acquired haemophilia a.,safety and efficacy of obizur have not been established in patients with baseline anti- porcine factor viii inhibitor titre greater than 20 bu.,obizur is not indicated for the treatment of congenital haemophilia a or von willebrand disease.

ELOCTATE efmoroctocog alfa (rhu) 1000 IU powder for injection, vial and diluent pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

eloctate efmoroctocog alfa (rhu) 1000 iu powder for injection, vial and diluent pre-filled syringe

sanofi-aventis australia pty ltd - efmoroctocog alfa, quantity: 1000 iu - drug delivery system - excipient ingredients: - eloctate is a long-acting antihaemophilic factor (recombinant) indicated in adults and children with haemophilia a (congenital factor viii deficiency) for: - control and prevention of bleeding episodes - routine prophylaxis to prevent or reduce the frequency of bleeding episodes - perioperative management (surgical prophylaxis). eloctate does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand's disease.

ELOCTATE efmoroctocog alfa (rhu) 2000 IU powder for injection vial and diluent pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

eloctate efmoroctocog alfa (rhu) 2000 iu powder for injection vial and diluent pre-filled syringe

sanofi-aventis australia pty ltd - efmoroctocog alfa, quantity: 2000 iu - drug delivery system - excipient ingredients: - eloctate is a long-acting antihaemophilic factor (recombinant) indicated in adults and children with haemophilia a (congenital factor viii deficiency) for: - control and prevention of bleeding episodes - routine prophylaxis to prevent or reduce the frequency of bleeding episodes - perioperative management (surgical prophylaxis). eloctate does not contain von willebrand factor, and therefore is not indicated in patients with von willebrand's disease.