Human Albumin Baxalta 50 g/l  Solution for Infusion Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin baxalta 50 g/l solution for infusion

baxalta innovations gmbh - plasma protein containing at least 95% human albumin - solution for infusion - 50 gram(s)/litre - blood substitutes and plasma protein fractions; albumin - plasma substitutes and plasma protein fractions - restoration and maintenance of circulating blood volume where volume deficiency has been demonstrated, and use of a colloid is appropriate.

Human Albumin Baxalta 200 g/l Solution for Infusion Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin baxalta 200 g/l solution for infusion

baxalta innovations gmbh - plasma protein containing at least 95% human albumin - solution for infusion - 200 gram(s)/litre - blood substitutes and plasma protein fractions; albumin - plasma substitutes and plasma protein fractions - restoration and maintenance of circulating blood volume where volume deficiency has been demonstrated, and use of a colloid is appropriate

HUMAN ALBUMIN 200 g/l Solution for Infusion Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin 200 g/l solution for infusion

baxter healthcare limited - plasma protein containing at least 95% human albumin - solution for infusion - 200 g/l

HUMAN ALBUMIN 50 g/l Solution for Infusion Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin 50 g/l solution for infusion

baxter healthcare limited - plasma protein containing at least 95% human albumin - solution for infusion - 50 g/l

Uman Albumin Solution for Infusion 200 gl Singapore - English - HSA (Health Sciences Authority)

uman albumin solution for infusion 200 gl

duo medical pte. ltd. - human albumin (human plasma protein containing at least 95% albumin) - infusion, solution - 200 g/l - human albumin (human plasma protein containing at least 95% albumin) 200 g/l

HUMAN ALBUMIN Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin

baxter healthcare limited - plasma protein containing at least 95% human albumin - solution for infusion - 50 g/l

HUMAN ALBUMIN Ireland - English - HPRA (Health Products Regulatory Authority)

human albumin

baxter healthcare limited - plasma protein containing at least 95% human albumin - solution for infusion - 200 g/l

OCTAPLAS- human plasma proteins solution United States - English - NLM (National Library of Medicine)

octaplas- human plasma proteins solution

octapharma usa inc - plasma protein fraction (human) (unii: 6d53g0fd0z) (plasma protein fraction (human) - unii:6d53g0fd0z) - plasma protein fraction (human) 11.5 g in 200 ml - octaplas is a solvent / detergent (s/d) treated, pooled human plasma indicated for: - replacement of multiple coagulation factors in patients with acquired deficiencies - due to liver disease - undergoing cardiac surgery and liver transplantation - plasma exchange in patients with thrombotic thrombocytopenic purpura (ttp) do not use octaplas in patients with: - iga deficiency - severe deficiency of protein s - history of hypersensitivity to fresh frozen plasma (ffp) or to plasma-derived products including any plasma protein - history of hypersensitivity reaction to octaplas risk summary animal reproduction studies have not been conducted with octaplas. it is not known whether octaplas can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. octaplas should be given to a pregnant woman only if clearly needed. the background risk of major birth defects and miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background

OCTAPLAS- human plasma proteins solution United States - English - NLM (National Library of Medicine)

octaplas- human plasma proteins solution

octapharma usa inc - plasma protein fraction (human) (unii: 6d53g0fd0z) (plasma protein fraction (human) - unii:6d53g0fd0z) - plasma protein fraction (human) 11.5 g in 200 ml - octaplas is a solvent / detergent (s/d) treated, pooled human plasma indicated for: - replacement of multiple coagulation factors in patients with acquired deficiencies - due to liver disease - undergoing cardiac surgery and liver transplantation - plasma exchange in patients with thrombotic thrombocytopenic purpura (ttp) do not use octaplas in patients with: - iga deficiency - severe deficiency of protein s - history of hypersensitivity to fresh frozen plasma (ffp) or to plasma-derived products including any plasma protein - history of hypersensitivity reaction to octaplas risk summary animal reproduction studies have not been conducted with octaplas. it is not known whether octaplas can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. octaplas should be given to a pregnant woman only if clearly needed. the background risk of major birth defects and miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background

OCTAPLAS- human plasma proteins solution United States - English - NLM (National Library of Medicine)

octaplas- human plasma proteins solution

octapharma usa inc - plasma protein fraction (human) (unii: 6d53g0fd0z) (plasma protein fraction (human) - unii:6d53g0fd0z) - plasma protein fraction (human) 11.5 g in 200 ml - octaplas is a solvent / detergent (s/d) treated, pooled human plasma indicated for: - replacement of multiple coagulation factors in patients with acquired deficiencies - due to liver disease - undergoing cardiac surgery and liver transplantation - plasma exchange in patients with thrombotic thrombocytopenic purpura (ttp) do not use octaplas in patients with: - iga deficiency - severe deficiency of protein s - history of hypersensitivity to fresh frozen plasma (ffp) or to plasma-derived products including any plasma protein - history of hypersensitivity reaction to octaplas risk summary animal reproduction studies have not been conducted with octaplas. it is not known whether octaplas can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. octaplas should be given to a pregnant woman only if clearly needed. the background risk of major birth defects and miscarriage for the indicated population is unknown. in the u.s. general population, the estimated background