Medication info

Vibran 10% Glucose Injection

Prescription medicationInjections정맥Approval withdrawn
Ingredient · strength
Glucose Monohydrate›11g / 100mL
Manufacturer / importer
비브라운코리아(주)
Appearance
A colorless and transparent infusion injection filled in a polyethylene container.
Packaging
Bottle - 500 milliliters/bottle, Bottle - 1000 milliliters/bottle
Approval status
Approval withdrawn

MFDS item code 200210365 · Notified 2002.05.06

This product's status changed to Approval withdrawn on 2024.12.13. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of hyperkalemia and circulatory collapse by providing energy.
Who receives it
Adults
Adult administration
Inject 20 to 500 mL intravenously. The rate of intravenous infusion should not exceed 0.5 g/kg per hour as glucose. Use an appropriate amount for dissolving or diluting the injection. Adjust according to age and symptoms.

Ingredients

Importer
비브라운코리아(주)

Efficacy & effects

Treatment of hyperkalemia and circulatory collapse by providing energy.

  • Hyperkalemia
  • circulatory collapse
  • hypoglycemia
View approved original text

1. This medication supplements the energy needed in hyperkalemia, circulatory collapse, and hypoglycemia. 2. It is also used for hydration and energy supply along with G, I, and K therapy for cardiac diseases. 3. Additionally, it helps in cases of drug or poison intoxication. In summary, this medication is used for hyperkalemia, circulatory collapse, hypoglycemia, treatment of heart diseases, hydration and energy supply, and drug and poison intoxication.

How it is given

Adult administration

Inject 20 to 500 mL intravenously. The rate of intravenous infusion should not exceed 0.5 g/kg per hour as glucose. Use an appropriate amount for dissolving or diluting the injection. Adjust according to age and symptoms.

Precautions

Care should be taken to avoid glass shards entering the injection solution when using this drug in ampoules. Extra caution is required when administering to children or the elderly. Patients receiving intravenous glucose should be aware that vitamin B1 may be rapidly consumed, leading to severe deficiency symptoms. This medication should not be administered to patients with certain conditions such as dehydration, fluid overload, hyperglycemia, acidosis, hypokalemia, hyperosmolar coma, or intolerance to glucose. It must not be used in patients with anuria or hepatic coma, or those allergic to this medication. It should be administered cautiously to patients who have deficiencies of potassium, phosphorus, or magnesium, or conditions such as renal failure, heart failure, nutritional deficiencies, or sepsis. Rapid or large infusions may result in electrolyte imbalances, dehydration, hyperosmolarity, and elevated substance levels in the blood, thus caution is advised. Long-term use of this medication may affect insulin secretion, and insulin should be provided as needed. During pregnancy, it should only be used when absolutely necessary, considering the risk to the fetus, and care should be taken with the glucose level of the mother and newborn during delivery. Newborns or premature infants are at higher risk of hypoglycemia or hyperglycemia, and their blood glucose levels should be closely monitored. Elderly patients, due to diminished physical function, should be used with extra caution. Overdosage may lead to hyperglycemia or diabetes symptoms, possibly requiring insulin treatment. It is advisable not to use this drug for subcutaneous injections, and any leftovers after opening should be discarded immediately. To reduce the risk of infection during injection, pay attention to hygiene; it should be warmed to body temperature when cold. When mixing with other medications, check for potential chemical interactions and side effects, and administer carefully. Also, take care not to introduce air bubbles that might lead to air embolism.

Side effects and when to seek care immediately

Mild side effects

  • Fever
  • phlebitis
  • thrombosis
  • blood leakage
  • injection site pain
  • uremia
  • electrolyte imbalance
  • congestion
  • pulmonary edema
  • hyperglycemia
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  • loss of kidney function
  • polyuria
  • hypokalemia
  • acidosis
  • dehydration
  • hyperosmolarity

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

Storage

This medication should be stored in a sealed container to prevent air and moisture exposure, at room temperature. Proper storage will help maintain the drug's effectiveness over time.

Appearance and packaging

Appearance

A colorless and transparent infusion injection filled in a polyethylene container.

Package unit

Bottle - 500 milliliters/bottle, Bottle - 1000 milliliters/bottle

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.

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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.