Volulyte 6% Solution for Infusion Malta - engelsk - Medicines Authority

volulyte 6% solution for infusion

fresenius kabi limited - poly(o-2-hydroxyethyl)starch; potassium chloride; magnesium chloride hexahydrate; sodium acetate trihydrate; sodium chloride - solution for infusion - poly(o-2-hydroxyethyl)starch 60 g; potassium chloride 0.3 g; magnesium chloride hexahydrate 0.3 g; sodium acetate trihydrate 4.63 g; sodium chloride 6.02 g - blood substitutes and perfusion solutions

LINEZOLID PANPHARMA INJECTION linezolid 200 mg in 100 mL solution for injection infusion bag Australia - engelsk - Department of Health (Therapeutic Goods Administration)

linezolid panpharma injection linezolid 200 mg in 100 ml solution for injection infusion bag

panpharma australia pty ltd - linezolid, quantity: 200 mg - injection, solution - excipient ingredients: glucose monohydrate; sodium citrate dihydrate; citric acid; hydrochloric acid; sodium hydroxide; water for injections - linezolid is indicated for the treatment of suspected or proven infections due to gram positive organisms resistant to multiple classes of antibiotics, including methicillin resistant staphylococcus species and vancomycin resistant enterococcus species. linezolid is active against gram-positive bacteria only. linezolid has no clinical activity against gram-negative pathogens. specific gram-negative therapy is required if a concomitant gram-negative pathogen is documented or suspected.

HEXTEND- hetastarch injection, solution USA - engelsk - NLM (National Library of Medicine)

hextend- hetastarch injection, solution

hospira, inc. - hetastarch (unii: 875y4127ea) (hetastarch - unii:875y4127ea) - hetastarch 6 g in 100 ml - hextend (6% hetastarch in lactated electrolyte injection) is indicated in the treatment of hypovolemia when plasma volume expansion is desired in settings where adequate alternative treatment is unavailable. it is not a substitute for blood or plasma. do not use hes products, including hextend, unless adequate alternative treatment is unavailable.

特慕血舒 10% 靜脈輸注液 Taiwan - kinesisk - 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

特慕血舒 10% 靜脈輸注液

台灣柏朗股份有限公司 台北市松山區健康路152號9樓 (23525106) - poly(o-2- hydroxyethyl)starch (hes)(molar subs 0.42; average molecular weight 130000 da);;sodium chloride;;potassium chloride;;calcium chloride dihydrate;;magnesium chloride hexahydrate (eq to magnesium chloride 6h2o);;sodium acetate trihydrate (eq to sodium acetate 3h2o );;malic acid - 注射液劑 - sodium acetate trihydrate (eq to sodium acetate 3h2o ) (4008000670) mg; calcium chloride dihydrate (4012000350) mg; magnesium chloride hexahydrate (eq to magnesium chloride 6h2o) (4012001550) mg; potassium chloride (4012001800) mg; sodium chloride (4012002100) mg; poly(o-2- hydroxyethyl)starch (hes)(molar subs 0.42; average molecular weight 130000 da) (9600009069) mg; malic acid (9600017800) mg - blood substitutes and plasma protein fractions - 單獨使用晶質輸注液無法治療之急性出血導致之低血容積病人,本品無法取代紅血球及血漿中的凝血因子。