Dextrose 5% DEMO solution for infusion Malta - English - Medicines Authority

dextrose 5% demo solution for infusion

demo s.a. pharmaceutical industry 21st km national road athens - lamia 14568 krioneri, greece - glucose anhydrous - solution for infusion - glucose anhydrous - general nutrients

GLUCOSE 50 % Israel - English - Ministry of Health

glucose 50 %

lapidot medical import and marketing ltd - glucose as monohydrate - concentrate for solution for infusion - glucose as monohydrate 50 % - glucose - glucose - high caloric carbohydrate infusion hypoglycaemia.

GLUCOSE 20 % Israel - English - Ministry of Health

glucose 20 %

lapidot medical import and marketing ltd - glucose as monohydrate - solution for infusion - glucose as monohydrate 20 % - glucose - glucose - high caloric carbohydrate infusion hypoglycaemia.

IONOSOL MB AND DEXTROSE- dextrose monohydrate, sodium lactate, potassium chloride, magnesium chloride, potassium phosphate, mono United States - English - NLM (National Library of Medicine)

ionosol mb and dextrose- dextrose monohydrate, sodium lactate, potassium chloride, magnesium chloride, potassium phosphate, mono

hospira, inc. - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok), sodium lactate (unii: tu7hw0w0qt) (sodium cation - unii:lyr4m0nh37, lactic acid, unspecified form - unii:33x04xa5at), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152, chloride ion - unii:q32zn48698), magnesium chloride (unii: 02f3473h9o) (magnesium cation - unii:t6v3lhy838, chloride ion - unii:q32zn48698), potassium phosphate, monobasic (unii: 4j9fj0hl51) (potassium cation - unii:295o53k152, phosph - dextrose monohydrate 5 g in 100 ml - ionosol mb and 5% dextrose injection is indicated for intravenous administration to infants for treatment of dehydration, acidosis, diarrhea, and burns, but only after administration of an initial priming solution: 15 ml of 5% dextrose and 0.45% sodium chloride injection/kg of body weight. in adults, ionosol mb and 5% dextrose injection is indicated postoperatively for intravenous fluid and electrolyte maintenance therapy, with a small amount of carbohydrate calories for reducing catabolism of endogenous protein reserves. solutions containing potassium are contraindicated in diseases where high potassium levels may be encountered.

DEXTROSE AND ELECTROLYTE NO. 48- sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium c United States - English - NLM (National Library of Medicine)

dextrose and electrolyte no. 48- sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium c

baxter healthcare corporation - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok), sodium lactate (unii: tu7hw0w0qt) (lactic acid - unii:33x04xa5at, sodium cation - unii:lyr4m0nh37), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152, chloride ion - unii:q32zn48698), magnesium chloride (unii: 02f3473h9o) (chloride ion - unii:q32zn48698, magnesium cation - unii:t6v3lhy838), potassium phosphate, monobasic (unii: 4j9fj0hl51) (phosphate ion - unii:nk08v8k8hr, potassium cation - unii:295 - dextrose monohydrate 5 g in 100 ml - 5% dextrose and electrolyte no. 48 injection (multiple electrolytes and dextrose injection, type 1, usp) is indicated as a source of water, electrolytes, and calories or as an alkalinizing agent. 5% dextrose and electrolyte no. 48 injection (multiple electrolytes and dextrose injection, type 1, usp) is contraindicated in patients

DEXTROSE injection, solution United States - English - NLM (National Library of Medicine)

dextrose injection, solution

b. braun medical inc. - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok) - dextrose monohydrate 70 g in 100 ml - this intravenous solution is indicated for use in adults and pediatric patients as a source of calories and water for hydration. solutions containing dextrose may be contraindicated in patients with hypersensitivity to corn products. administration of solutions containing hypertonic dextrose is contraindicated in patients with intracranial or intraspinal hemorrhage, diabetic coma or delirium tremens, especially if such patients are already dehydrated. there is no specific pediatric dose. the dose is dependent on weight, clinical condition, and laboratory results. follow recommendations of appropriate pediatric reference text. (see warnings and precautions .)

DIANEAL PD-2 Peritoneal Dialysis with 1.5% w/v Glucose Solution Freeline Solo Twin Bag Australia - English - Department of Health (Therapeutic Goods Administration)

dianeal pd-2 peritoneal dialysis with 1.5% w/v glucose solution freeline solo twin bag

vantive pty ltd - glucose monohydrate, quantity: 15 g/l; sodium chloride, quantity: 5.38 g/l; sodium lactate, quantity: 4.48 g/l; calcium chloride dihydrate, quantity: 257 mg/l; magnesium chloride hexahydrate, quantity: 50.8 mg/l - solution, irrigation - excipient ingredients: hydrochloric acid; water for injections - dianeal low calcium peritoneal dialysis solution is indicated for use in chronic renal failure patients being maintained on continuous ambulatory peritoneal dialysis or intermittent peritoneal dialysis and/or automated peritoneal dialysis and can also be used for acute renal failure.

DIANEAL PD-2 Peritoneal Dialysis with 4.25% w/v Glucose Solution Freeline Solo Twin Bag Australia - English - Department of Health (Therapeutic Goods Administration)

dianeal pd-2 peritoneal dialysis with 4.25% w/v glucose solution freeline solo twin bag

vantive pty ltd - glucose monohydrate, quantity: 42.5 g/l; sodium chloride, quantity: 5.38 g/l; sodium lactate, quantity: 4.48 g/l; calcium chloride dihydrate, quantity: 257 mg/l; magnesium chloride hexahydrate, quantity: 50.8 mg/l - solution, irrigation - excipient ingredients: hydrochloric acid; water for injections - dianeal low calcium peritoneal dialysis solution is indicated for use in chronic renal failure patients being maintained on continuous ambulatory peritoneal dialysis or intermittent peritoneal dialysis and/or automated peritoneal dialysis and can also be used for acute renal failure.

DIANEAL PD-2 Peritoneal Dialysis with 2.5% w/v Glucose Solution Freeline Solo Twin Bag Australia - English - Department of Health (Therapeutic Goods Administration)

dianeal pd-2 peritoneal dialysis with 2.5% w/v glucose solution freeline solo twin bag

vantive pty ltd - glucose monohydrate, quantity: 25 g/l; sodium chloride, quantity: 5.38 g/l; sodium lactate, quantity: 4.48 g/l; calcium chloride dihydrate, quantity: 257 mg/l; magnesium chloride hexahydrate, quantity: 50.8 mg/l - solution, irrigation - excipient ingredients: hydrochloric acid; water for injections - dianeal low calcium peritoneal dialysis solution is indicated for use in chronic renal failure patients being maintained on continuous ambulatory peritoneal dialysis or intermittent peritoneal dialysis and/or automated peritoneal dialysis and can also be used for acute renal failure.

DIANEAL PD-2 Peritoneal Dialysis with 0.55% w/v Glucose Solution Freeline Solo Twin Bag Australia - English - Department of Health (Therapeutic Goods Administration)

dianeal pd-2 peritoneal dialysis with 0.55% w/v glucose solution freeline solo twin bag

vantive pty ltd - glucose monohydrate, quantity: 5.5 g/l; sodium chloride, quantity: 5.38 g/l; sodium lactate, quantity: 4.48 g/l; calcium chloride dihydrate, quantity: 257 mg/l; magnesium chloride hexahydrate, quantity: 50.8 mg/l - solution, irrigation - excipient ingredients: hydrochloric acid; water for injections - dianeal low calcium peritoneal dialysis solution is indicated for use in chronic renal failure patients being maintained on continuous ambulatory peritoneal dialysis or intermittent peritoneal dialysis and/or automated peritoneal dialysis and can also be used for acute renal failure.