KOVALTRY 2000 IU Izraelis - anglų - Ministry of Health

kovaltry 2000 iu

bayer israel ltd - recombinant human coagulation factor viii - powder and solvent for solution for injection - recombinant human coagulation factor viii 2000 iu - coagulation factor viii - treatment and prophylaxis of bleeding in patients with haemophilia a (congenital factor viii deficiency). kovaltry can be used for all age groups.

KOVALTRY 250 IU Izraelis - anglų - Ministry of Health

kovaltry 250 iu

bayer israel ltd - recombinant human coagulation factor viii - powder and solvent for solution for injection - recombinant human coagulation factor viii 250 iu - coagulation factor viii - treatment and prophylaxis of bleeding in patients with haemophilia a (congenital factor viii deficiency). kovaltry can be used for all age groups.

Immunate 250 IU FVIII/190 IU VWF powder and solvent for solution for injection Malta - anglų - Medicines Authority

immunate 250 iu fviii/190 iu vwf powder and solvent for solution for injection

takeda manufacturing austria ag industriestrasse 67, a-1221, vienna, austria - factor viii, human, von willebrand - powder and solvent for solution for injection - factor viii, human 250 iu von willebrand factor, human 190 iu - antihemorrhagics

Immunate 500 IU FVIII/375 IU VWF powder and solvent for solution for injection Malta - anglų - Medicines Authority

immunate 500 iu fviii/375 iu vwf powder and solvent for solution for injection

takeda manufacturing austria ag industriestrasse 67, a-1221, vienna, austria - factor viii, human, von willebrand - powder and solvent for solution for injection - factor viii, human 500 iu von willebrand factor, human 375 iu - antihemorrhagics

Immunate 1000 IU FVIII/750 IU VWF powder and solvent for solution for injection Malta - anglų - Medicines Authority

immunate 1000 iu fviii/750 iu vwf powder and solvent for solution for injection

takeda manufacturing austria ag industriestrasse 67, a-1221, vienna, austria - factor viii, human, von willebrand - powder and solvent for solution for injection - factor viii, human 1000 iu von willebrand factor, human 750 iu - antihemorrhagics

BENEFIX  - (500IU) KIT Kanada - anglų - Health Canada

benefix - (500iu) kit

wyeth canada - coagulation factor ix (recombinant); water - kit - 500unit; 5ml - coagulation factor ix (recombinant) 500unit; water 5ml - hemostatics

MONONINE- coagulation factor ix human kit Jungtinės Valstijos - anglų - NLM (National Library of Medicine)

mononine- coagulation factor ix human kit

csl behring llc - coagulation factor ix human (unii: 6u90y1795t) (coagulation factor ix human - unii:6u90y1795t) - coagulation factor ix human 500 [iu] in 5 ml - mononine is indicated for the prevention and control of bleeding in factor ix deficiency, also known as hemophilia b or christmas disease. mononine is not indicated in the treatment or prophylaxis of hemophilia a patients with inhibitors to factor viii. mononine contains non-detectable levels of factors ii, vii and x (<0.0025 iu per factor ix unit using standard coagulation assays) and is, therefore, not indicated for replacement therapy of these clotting factors. mononine is also not indicated in the treatment or reversal of coumarin-induced anticoagulation or in a hemorrhagic state caused by hepatitis-induced lack of production of liver dependent coagulation factors. known hypersensitivity to mouse protein is a contraindication to mononine.

RECOMBINATE- antihemophilic factor recombinant Jungtinės Valstijos - anglų - NLM (National Library of Medicine)

recombinate- antihemophilic factor recombinant

baxter healthcare corporation - antihemophilic factor, human recombinant (unii: p89dr4ny54) (antihemophilic factor, human recombinant - unii:p89dr4ny54) - antihemophilic factor, human recombinant 25 [iu] in 1 ml - the use of recombinate [antihemophilic factor (recombinant)] is indicated in hemophilia a (classical hemophilia) for the prevention and control of hemorrhagic episodes.2 recombinate is also indicated in the perioperative management of patients with hemophilia a (classical hemophilia). recombinate can be of therapeutic value in patients with acquired factor viii inhibitors not exceeding 10 bethesda units per ml.3   in clinical studies with recombinate, patients with inhibitors who were entered into the previously treated patient trial and those previously untreated children who have developed inhibitor activity on study, showed clinical hemostatic response when the titer of inhibitor was less than 10 bethesda units per ml. however, in such uses, the dosage of recombinate should be controlled by frequent laboratory determinations of circulating factor viii levels as well as the clinical status of the patient. recombinate is not indicated in von willebrand’s disease. recombinate is contraindicated in patients w

Octanate 50IU/ml powder and solvent for solution for injection  (5ml vial) Malta - anglų - Medicines Authority

octanate 50iu/ml powder and solvent for solution for injection (5ml vial)

octapharma (ip) sprl alle de la recherche 65, 1070 (anderlecht), belgium - factor viii, human - powder and solvent for solution for injection - factor viii, human 50 iu/ml - antihemorrhagics

Octanate 50IU/ml powder and solvent for solution for injection  (10ml vial) Malta - anglų - Medicines Authority

octanate 50iu/ml powder and solvent for solution for injection (10ml vial)

octapharma (ip) sprl alle de la recherche 65, 1070 (anderlecht), belgium - factor viii, human - powder and solvent for solution for injection - factor viii, human 50 iu - antihemorrhagics