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Dextrose is a form of glucose (sugar). Dextrose 5% in water is injected into a vein through an IV to replace lost fluids and provide carbohydrates to the body. Dextrose 5% in water is used to treat low blood sugar (hypoglycemia), insulin shock, or dehydration (fluid loss). Dextrose 5% in water is also given for nutritional support to patients.
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Dextrose in Ringer's Description. Each 100 mL of 5% Dextrose in Ringer's Injection contains: Hydrous Dextrose USP 5 g; Sodium Chloride USP 0.86 g; Calcium Chloride Dihydrate USP 0.033 g; Potassium Chloride USP 0.03 g; Water for Injection USP qs. pH: 4.3 (3.5-6.5); Calories per liter: 170. Calculated Osmolarity: 560 mOsmol/liter, hypertonic.
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5% Dextrose Injection, USP can cause fetal harm when administered to a pregnant woman. Lactated Ringer's and 5% Dextrose Injection, USP should be given during pregnancy only if the potential benefit justifies the potential risk to the fetus. Labor and Delivery . Intrapartum maternal intravenous infusion of glucose-containing solutions may produce
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The coefficient of variability of blood glucose in the postprotocol group (n = 53) was decreased compared with the preprotocol group (n = 52), 40.9% versus 49.3%, respectively (P = .048).
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Observe the usual precautions and contraindications associated with dextrose in patients receiving 10% dextran 40 in 5% dextrose injection. Cardiac Patients. Dextran 40 is hazardous to heart failure patients because of the plasma volume expanding effect, especially when administered in sodium chloride. (See Sodium Content under Cautions.)
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Dextrose Injection, USP is a sterile, nonpyrogenic solution for fluid replenishment and caloric supply in single dose containers for intravenous administration. It contains no antimicrobial agents. Composition, osmolarity, pH, and caloric content are shown in Table 1. Table 1 . Size (mL) *Dextrose Hydrous, USP (g/L)
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2.1 Important Administration Instructions. 10% Dextrose Injection is intended for intravenous use. Peripheral administration of 5% dextrose is generally acceptable, however, consider central vein when administering more than 5% dextrose or with an osmolarity of at least 900 mOsm/L or when there is peripheral vein irritation, phlebitis, and/or associated pain [see Warnings and Precautions ()].
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The Dextrose monograph will be incorporated into and become official with the Second Supplement to USP 39-NF 34. The official implementation date for the omission of the Heavy Metals test is January 1, 2018. Should you have any questions about the Dextrose monograph, please contact Tong (Jenny) Liu (240-221-2072 or [email protected] ).
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Call 800-438-1985 *. *Contact Medical Information. 8AM-9PM ET Monday to Friday; excluding holidays. dextran 40 () Description DESCRIPTION LMD (dextran 40) is a sterile, nonpyrogenic preparation of low molecular weight dextran (average mol. wt. 40,000) in 5% Dextrose Injection or 0.9% Sodium Chloride Injection.
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- Maximum dosage 1.5 -3.0 gram dextrose / kg bodyweight / day. CONTRAINDICATION : Patient with hyperhydration, acidosis, diabetes mellitus, and mal-absorption glucose - galactose syndrome. SIDE EFFECTS : - A low pH solution (3,5-5,0) may causes thrombophebitis. - Reactions that may occur because of the solution or the technique of administration
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5% Dextrose and 0.45% Sodium Chloride Injection, USP is supplied in single-dose flexible plastic containers as follows: List No. Product Name Container Size (mL) 7926 5% Dextrose and 500 & 1000 0.45% Sodium Chloride Injection, USP Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat.
Dextrose 40
Caution advised, to avoid air embolism, when infusing medication. Monitor glucose levels and for possible hyperglycemia when treating pediatric patients. Dextrose injection contains aluminum that may be toxic; patients with impaired renal function, and preterm infants, at higher risk;. limit aluminum to <4 mcg/kg/day.
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40% Dextrose Concentrated Solution to the Post-correction Blood Sugar. Pekat Dekstrosa 40% secara Intravena Infus dan Intravena Bolus terhadap Respon Gula Darah Pascakoreksi
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2.1 Important Preparation and Administration Instructions . Dextrose Injection is supplied in the following five strengths: 20%, 30%, 40%, 50% and 70% [see How Supplied/Storage and Handling ()]. Prior to administration, Dextrose Injection must be diluted with other compatible intravenous fluids or used as an admixture with amino acids. It is not for direct intravenous infusion.
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L-glucose is a synthesized enantiomer that is used as a low-calorie sweetener and laxative. The unspecified form of glucose is commonly supplied as an injection for nutritional supplementation or metabolic disorders where glucose levels are improperly regulated. Glucose is listed on the World Health Organization's List of Essential Medicines. Type