Medication info

Daehan 5% Glucose in Physiological Saline

Prescription medication정맥
Ingredient · strength
Glucose›50g / 1000mLSodium Chloride›9g / 1000mL
Manufacturer / importer
대한약품공업(주)
Appearance
A colorless and transparent liquid with a slight salty and sweet taste, filled in a colorless and transparent glass or polypropylene, multilayer film plastic container.
Packaging
500mL/bottle, 500mL/bag, 1000mL/bottle, 1000mL/bag
Approval status
Active

MFDS item code 196800019 · Notified 1968.12.04 · Insurance code 645100242,645100252

Summary

Main use
Improvement of condition through fluid and electrolyte replenishment and energy supply for dehydration and pre- and post-operative management
Who receives it
Adults · Children
Adult administration
Typically, adults receive an intravenous infusion of 500–1,000mL per day, divided into 2–3 doses. The administration rate is 250–500mL per hour (60–120 drops per minute), and in elderly patients, it should be 250mL per hour (60 drops per minute).
Child administration
For infants and young children, the administration rate should be 15–60mL per hour (4–15 drops per minute).

Ingredients

Manufacturer
대한약품공업(주)

Efficacy & effects

Improvement of condition through fluid and electrolyte replenishment and energy supply for dehydration and pre- and post-operative management

  • Dehydration
View approved original text

This medication is used to replenish fluids and electrolytes that have been depleted due to dehydration or before and after surgery. It also supplies the necessary energy to patients, assisting in their recovery. Therefore, it is effective in maintaining the balance of fluids and electrolytes and improving energy supply in the body.

How it is given

Adult administration

Typically, adults receive an intravenous infusion of 500–1,000mL per day, divided into 2–3 doses. The administration rate is 250–500mL per hour (60–120 drops per minute), and in elderly patients, it should be 250mL per hour (60 drops per minute).

Child administration

For infants and young children, the administration rate should be 15–60mL per hour (4–15 drops per minute).

Precautions

This medication is an intravenous solution containing glucose, which may increase the consumption of vitamin B1 upon administration, potentially leading to fatal vitamin B1 deficiency. This medication should not be used in patients with excessive fluid retention, hypertonic dehydration, or low potassium or high sodium levels in the blood. It should be administered with caution in patients with impaired kidney function, weak heart function, hypertonic dehydration, low urine output due to urinary obstruction, diabetes patients, patients with high blood chloride levels, and those with very low blood sodium levels. If this medication is administered in excessive amounts or too rapidly, it can cause edema in the brain or lungs, peripheral edema, acidosis, water intoxication, etc. Particularly, in newborns or premature infants, rapid administration can lead to water intoxication; thus, caution is required. There is also a risk of thrombosis at the intravenous injection site, so monitoring is necessary. During administration, blood glucose, electrolyte levels in the blood, and fluid balance should be checked regularly. During pregnancy, the risks to the fetus and treatment effectiveness must be carefully considered, and during labor, there is a risk of hyperglycemia and hypoglycemia for both the mother and newborn, requiring monitoring. Newborns, particularly premature or low-birth-weight infants, require meticulous management due to difficulties in blood sugar control, as hypoglycemia can cause severe brain damage. In infants and the elderly, caution should be exercised to avoid rapid or prolonged administration; in the elderly, especially those with weak heart and kidney function, care should be taken to avoid circulatory overload. In case of overdose, diuretics should be used to expel excessive fluid. Before administration, skin or equipment should be thoroughly disinfected to prevent infection, and it should be warmed to body temperature if stored cold before use. Once opened, it should be used immediately, and any leftover medication should not be used; during infusion, it should be administered slowly via intravenous injection. To prevent air embolism, care should be taken not to inject air from the container, and using multiple containers in series should be avoided.

Side effects and when to seek care immediately

Serious side effects

Peripheral edema, pulmonary edema

Mild side effects

  • Cerebral edema
  • pulmonary edema
  • peripheral edema
  • acidosis
  • water intoxication
  • thrombosis

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a sealed container at room temperature between 1 and 30 degrees Celsius. Storing it this way helps maintain the medication's effectiveness and safety.

Appearance and packaging

Appearance

A colorless and transparent liquid with a slight salty and sweet taste, filled in a colorless and transparent glass or polypropylene, multilayer film plastic container.

Package unit

500mL/bottle, 500mL/bag, 1000mL/bottle, 1000mL/bag

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.