CSL PANAMA HUMAN COAGULATION FACTOR VIII FOR INJECTION 500IU Австралия - английский - Department of Health (Therapeutic Goods Administration)

csl panama human coagulation factor viii for injection 500iu

csl behring australia pty ltd - factor viii, quantity: 500 iu - injection, solution - excipient ingredients: water for injections - human coagulation factor viii is indicated for the treatment and prophylaxis of bleeding associated with factor viii deficiency due to haemophilia a.

CSL COLOMBIA HUMAN COAGULATION FACTOR VIII FOR INJECTION 500IU Австралия - английский - Department of Health (Therapeutic Goods Administration)

csl colombia human coagulation factor viii for injection 500iu

csl behring australia pty ltd - factor viii, quantity: 500 iu - injection, solution - excipient ingredients: water for injections - human coagulation factor viii is indicated for the treatment and prophylaxis of bleeding associated with factor viii deficiency due to haemophilia a.

CSL New Zealand MonoFIX-VF Human Coagulation Factor IX  1000 IU powder for injection (100 IU/mL) Австралия - английский - Department of Health (Therapeutic Goods Administration)

csl new zealand monofix-vf human coagulation factor ix 1000 iu powder for injection (100 iu/ml)

csl behring australia pty ltd - factor ix, quantity: 1000 iu - injection, diluent for - excipient ingredients: water for injections - monofix-vf is indicated for the treatment of haemorrhages, for use in surgery, and as prophylaxis in patients with haemophilia b. monofix-vf is not indicated for the treatment of factor ii, vii or x deficiencies because it does not contain therapeutic levels of these coagulation factors. monofix-vf is not indicated for the treatment of haemophilia a patients with factor viii inhibitors.

CSL New Zealand MonoFIX-VF Human Coagulation Factor IX  500 IU powder for injection (100 IU/mL) Австралия - английский - Department of Health (Therapeutic Goods Administration)

csl new zealand monofix-vf human coagulation factor ix 500 iu powder for injection (100 iu/ml)

csl behring australia pty ltd - factor ix, quantity: 500 iu - injection, diluent for - excipient ingredients: water for injections - monofix-vf is indicated for the treatment of haemorrhages, for use in surgery, and as prophylaxis in patients with haemophilia b. monofix-vf is not indicated for the treatment of factor ii, vii or x deficiencies because it does not contain therapeutic levels of these coagulation factors. monofix-vf is not indicated for the treatment of haemophilia a patients with factor viii inhibitors.

CSL Hong Kong Aleviate Human Coagulation Factor VIII 250IU/von Willebrand factor 500IU complex, Powder for injection (50 IU/mL FVIII) Австралия - английский - Department of Health (Therapeutic Goods Administration)

csl hong kong aleviate human coagulation factor viii 250iu/von willebrand factor 500iu complex, powder for injection (50 iu/ml fviii)

csl behring australia pty ltd - factor viii, quantity: 250 iu; von willebrand factor, quantity: 500 iu - injection, solution - excipient ingredients: water for injections - aleviate is indicated for: ? the treatment of bleeding episodes including surgical bleeding in patients with von willebrand disease when desmopressin (ddavp) treatment is ineffective or contraindicated. ? the treatment and prophylaxis of bleeding associated with factor fviii deficiency due to haemophilia a.

HAEMOCTIN SDH 250 IU Израиль - английский - Ministry of Health

haemoctin sdh 250 iu

kamada ltd, israel - human plasma coagulation factor viii - powder for solution for injection - human plasma coagulation factor viii 50 iu/ml - coagulation factor viii - coagulation factor viii - treatment and prophylaxis of bleeding: in patients with haemophilia a (congenital factor viii deficiency) in patient with acquired factor viii deficiency. haemoctin is not effective in controlling the bleeding of patients with von willebrond`s disease.

HAEMOCTIN SDH 500 IU Израиль - английский - Ministry of Health

haemoctin sdh 500 iu

kamada ltd, israel - human plasma coagulation factor viii - powder and solvent for solution for injection - human plasma coagulation factor viii 50 iu/ml - coagulation factor viii - coagulation factor viii - treatment and prophylaxis of bleeding: in patients with haemophilia a (congenital factor viii deficiency) in patient with acquired factor viii deficiency.haemoctin is not effective in controlling the bleeding of patients with von willebrond`s disease.

HAEMOCTIN SDH 1000 IU Израиль - английский - Ministry of Health

haemoctin sdh 1000 iu

kamada ltd, israel - human plasma coagulation factor viii - powder and solvent for solution for injection - human plasma coagulation factor viii 100 iu/ml - coagulation factor viii - coagulation factor viii - treatment and prophylaxis of bleeding: in patients with haemophilia a (congenital factor viii deficiency) in patient with acquired factor viii deficiency.haemoctin is not effective in controlling the bleeding of patients with von willebrond`s disease.

ALPHANATE (antihemophilic factor/von willebrand factor complex- human kit Соединенные Штаты - английский - NLM (National Library of Medicine)

alphanate (antihemophilic factor/von willebrand factor complex- human kit

grifols usa, llc - human coagulation factor viii/von willebrand factor complex (unii: 5t6b772r4q) (human coagulation factor viii/von willebrand factor complex - unii:5t6b772r4q) - human coagulation factor viii/von willebrand factor complex 250 [iu] in 5 ml - alphanate, (antihemophilic factor/von willebrand factor complex [human]), is indicated for: - control and prevention of bleeding episodes and perioperative management in adult and pediatric patients with factor viii (fviii) deficiency due to hemophilia a. - surgical and/or invasive procedures in adult and pediatric patients with von willebrand disease (vwd) in whom desmopressin (ddavp) is either ineffective or contraindicated.  it is not indicated for patients with severe vwd (type 3) undergoing major surgery. alphanate is contraindicated in patients who have manifested life-threatening immediate hypersensitivity reactions, including anaphylaxis, to the product or its components [see adverse reactions (6) ]. pregnancy category c.  animal reproduction studies have not been conducted with alphanate.  it is also not known whether alphanate can cause fetal harm when administered to a pregnant woman or affect reproductive capacity.  alphanate should be given to a pregnant woman only if clearly needed.   no human o