INTRAGAM P immunoglobulin-normal (human) 30g/500mL for intravenous use injection vial Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

intragam p immunoglobulin-normal (human) 30g/500ml for intravenous use injection vial

csl behring australia pty ltd - normal immunoglobulin, quantity: 60 mg/ml - injection, solution - excipient ingredients: maltose; human immunoglobulin a; water for injections - intragam p is indicated in replacement immunoglobulin g (igg) therapy in: primary immunodeficiency; myeloma and chronic lymphatic leukaemia with severe secondary hypogammaglobulinaemia and recurrent infections; congenital acquired immune deficiency syndrome with recurrent infections. indications as at 21 july 2000: replacement igg therapy in: primary immunodeficiency; myeloma and chronic lymphatic leukaemia with severe secondary hypogammaglobulinaemia and recurrent infections; congenital acquired immune deficiency syndrome with recurrent infections. immunomodulatory therapy in: idiopathic thrombocytopenic purpura (itp), in adults or children at high risk of bleeding or prior to surgery to correct platelet count; allogenic bone marrow transplantation; kawasaki disease. indications as at 25 february 2003: for replacement immunoglobulin g (igg) therapy in: primary immunodeficiency; myeloma and chronic lymphatic leukaemia with severe secondary hypogammaglobulinaemia and recurrent infections, and; congenital acquired immune deficiency syndrome with recurrent infections. for immunomodulatory therapy in: idiopathic thrombocytopenic purpura (itp) in adults or children at high risk of bleeding or prior to surgery to correct platelet count; allogeneic bone marrow transplantation; kawasaki disease, and; guillain-barre syndrome (gbs).

Tetanus Gamma 250 IU/1 ml Solution for injection for intramuscular use Malta - anglès - Medicines Authority

tetanus gamma 250 iu/1 ml solution for injection for intramuscular use

kedrion s.p.a loc. ai conti, 55051 castelvecchio pascoli, barga - lucca, italy - human plasma, protein - solution for injection - human plasma protein 100-180 mg - immune sera and immunoglobulins

Hepatect CP 50 IU/ml; solution for infusion Irlanda - anglès - HPRA (Health Products Regulatory Authority)

hepatect cp 50 iu/ml; solution for infusion

biotest pharma gmbh - human plasma protein; hbs antibodies - solution for infusion - 50 international unit(s)/millilitre - specific immunoglobulins; hepatitis b immunoglobulin

GAMMAGARD S/D 0.5 g/30 m Micromol Pdr+Solv for soln for Inf Irlanda - anglès - HPRA (Health Products Regulatory Authority)

gammagard s/d 0.5 g/30 m micromol pdr+solv for soln for inf

baxter healthcare limited - human plasma protein >90% gamma globulin - pdr+solv for soln for inf - 0.5 g/30 m micromol

ZUTECTRA SOLUTION FOR INJECTION 500 IUML Singapur - anglès - HSA (Health Sciences Authority)

zutectra solution for injection 500 iuml

eshcol pharmaceutical group singapore pte ltd - human hepatitis b immunoglobulin in 150g/l human plasma protein (igg ≥ 96%) - injection - 500 iu/ml - human hepatitis b immunoglobulin in 150g/l human plasma protein (igg ≥ 96%) 500 iu/ml

Tetagam P, prefilled syringeSolution for injection for intramuscular use Irlanda - anglès - HPRA (Health Products Regulatory Authority)

tetagam p, prefilled syringesolution for injection for intramuscular use

csl behring gmbh - human plasma protein - solution for injection - 250 international unit(s)/millilitre - specific immunoglobulins; tetanus immunoglobulin

VARIZIG (varicella zoster immune globulin- human solution Estats Units - anglès - NLM (National Library of Medicine)

varizig (varicella zoster immune globulin- human solution

aptevo biotherapeutics llc - human varicella-zoster immune globulin (unii: 33t61iwl27) (human varicella-zoster immune globulin - unii:33t61iwl27) - human varicella-zoster immune globulin 125 [iu] - varizig® [varicella zoster immune globulin (human)] is indicated for post-exposure prophylaxis of varicella in high risk individuals. high risk groups include: - immunocompromised children and adults, - newborns of mothers with varicella shortly before or after delivery, - premature infants, - neonates and infants less than one year of age, - adults without evidence of immunity, - pregnant women. varizig administration is intended to reduce the severity of varicella. administer varizig as soon as possible following varicella zoster virus (vzv) exposure, ideally within 96 hours for greatest effectiveness. - there is no convincing evidence that varizig reduces the incidence of chickenpox infection after exposure to vzv. - there is no convincing evidence that established infections with vzv can be modified by varizig administration. - there is no indication for the prophylactic use of varizig in immunodeficient children or adults when there is a past history of varicella, unless the patient is undergoing bone m

Octagam 10% Solution for Infusion 100mg/ml (20ml vial) Malta - anglès - Medicines Authority

octagam 10% solution for infusion 100mg/ml (20ml vial)

octapharma (ip) sprl alle de la recherche 65, 1070 (anderlecht), belgium - immunoglobulin g, human - solution for infusion - immunoglobulin g, human 100 mg i/ml - immune sera and immunoglobulins

Tetagam P Solution for Injection for intramuscular use 250IU/ml Malta - anglès - Medicines Authority

tetagam p solution for injection for intramuscular use 250iu/ml

csl behring gmbh emil-von-behring-strasse 76, 35041 marburg, germany - immunoglobulin tetanus, human - solution for injection - immunoglobulin tetanus, human 250 iu - immune sera and immunoglobulins

Tetagam P Solution for Injection for intramuscular use 250IU/ml Malta - anglès - Medicines Authority

tetagam p solution for injection for intramuscular use 250iu/ml

csl behring gmbh emil-von-behring-strasse 76, 35041 marburg, germany - immunoglobulin tetanus, human - solution for injection - immunoglobulin tetanus, human 250 iu - immune sera and immunoglobulins