Nový Zéland - angličtina - Medsafe (Medicines Safety Authority)

baxter healthcare ltd - glucose monohydrate 25% - solution for infusion - 25 % - active: glucose monohydrate 25% - hypertonic infusion solutions are indicated: - as a source of energy incorporated with parenteral nutrition with minimal dilution effect - for use with an appropriate protein (nitrogen) source in the prevention of nitrogen loss or in the treatment of negative nitrogen balance in patients where: a) the alimentary tract cannot or should not be used b) gastrointestinal absorption of protein is impaired c) metabolic requirements for protein are substantially increased, as with extensive burns.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 10 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 20 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 250 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 1000 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 100 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

b braun australia pty ltd - water for injections, quantity: 500 ml - injection, solvent for - excipient ingredients: - water for injections is used for the reconstitution and preparation of aqueous injections

Spojené státy - angličtina - NLM (National Library of Medicine)

hospira, inc. - dextrose, unspecified form (unii: iy9xdz35w2) (dextrose, unspecified form - unii:iy9xdz35w2), sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698), sodium acetate anhydrous (unii: nvg71zz7p0) (sodium cation - unii:lyr4m0nh37), sodium gluconate (unii: r6q3791s76) (sodium cation - unii:lyr4m0nh37), potassium chloride (unii: 660yq98i10) (potassium cation - unii:295o53k152), magnesium chloride (unii: 02f3473h9o) (magnesium cation - unii:t6v3lhy838) - dextrose 5 g in 100 ml - normosol-r and 5% dextrose injection is indicated for replacement of acute extracellular fluid volume losses in surgery, trauma, burns or shock. normosol-r and 5% dextrose also can be used as an adjunct to restore a decrease in circulatory volume in patients with moderate blood loss. the solution is not intended to supplant transfusion of whole blood or packed red cells in the presence of uncontrolled hemorrhage or severe reductions of red cell volume. none known.

Spojené státy - angličtina - NLM (National Library of Medicine)

hospira, inc. - dextrose monohydrate (unii: lx22yl083g) (anhydrous dextrose - unii:5sl0g7r0ok), sodium chloride (unii: 451w47iq8x) (sodium cation - unii:lyr4m0nh37, chloride ion - unii:q32zn48698), potassium acetate (unii: m911911u02) (potassium cation - unii:295o53k152), magnesium acetate (unii: 0e95jzy48k) (magnesium cation - unii:t6v3lhy838) - dextrose monohydrate 5 g in 100 ml - normosol-m and 5% dextrose injection (multiple electrolytes and 5% dextrose injection type 1, usp) is indicated for parenteral maintenance of routine daily fluid and electrolyte requirements with minimal carbohydrate calories from dextrose. magnesium in the formula may help to prevent iatrogenic magnesium deficiency in patients receiving prolonged parenteral therapy. none known.

Spojené státy - angličtina - NLM (National Library of Medicine)

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.