Medication info

DHC Dex Solution 0.1%

Prescription medication주사
Ingredient · strength
Sodium Chloride›21.27g / 100mLPotassium Chloride›0.522g / 100mLCalcium Chloride Hydrate›0.772g / 100mLMagnesium Chloride›0.356g / 100mLSodium Acetate Hydrate›2.853g / 100mLGlucose›3.5g / 100mL
Manufacturer / importer
대한약품공업(주)
Appearance
Colorless and transparent liquid filled in a plastic container
Packaging
5.5L, 10L
Approval status
Active

MFDS item code 200100331 · Notified 2001.10.11 · Insurance code 645101230

Summary

Main use
Effectiveness in managing blood sugar levels and improving electrolyte imbalances (hyperkalemia, hypermagnesemia)
Who receives it
Adults
Adult administration
Select an appropriate alkaline solution for dialysis based on the patient’s condition and the type of dialysis machine being used, and dilute with this solution and purified water.

Ingredients

Manufacturer
대한약품공업(주)

Efficacy & effects

Effectiveness in managing blood sugar levels and improving electrolyte imbalances (hyperkalemia, hypermagnesemia)

  • Chronic renal failure
  • difficulty managing blood sugar levels
  • hyperkalemia
  • hypermagnesemia
  • hypercalcemia
View approved original text

This medication is used for patients with chronic renal failure undergoing dialysis who have difficulty managing blood sugar levels, or for those who are not alleviated from hyperkalemia or hypermagnesemia by existing dialysate, or for patients concerned about hypercalcemia. In other words, it helps in managing blood sugar levels and improving electrolyte balance, making dialysis treatment safer and more effective.

How it is given

Adult administration

Select an appropriate alkaline solution for dialysis based on the patient’s condition and the type of dialysis machine being used, and dilute with this solution and purified water.

Precautions

This medication should be used with caution in patients with severe liver impairment or severe diabetes. In these patients, the drug may not be metabolized properly, causing symptoms such as hypotension. Additionally, patients taking digitalis preparations should be careful as low serum potassium levels may lead to symptoms of drug toxicity. Hypoglycemia or hyperglycemia may occur during or after dialysis, so it's important to closely monitor blood sugar changes and take appropriate action if abnormalities are detected. If weight gain or increased blood pressure occurs, management may be needed such as adjusting fluid intake or removing fluid from the body through dialysis. Bone diseases such as osteoporosis or osteomalacia may develop due to calcium metabolism disorders, so Vitamin D3 preparations should be administered if necessary. Moreover, the occurrence of ectopic calcification is possible, making it crucial to maintain serum phosphorus levels within normal ranges. Symptoms of dialysis disequilibrium syndrome, such as headache, nausea, and convulsions, may present, so dialysis intensity should be adjusted if such symptoms are observed. Hypotension or shock symptoms may arise as well, necessitating stopping dialysis or administering fluids and antihypertensive agents if symptoms occur. Pregnant women or women who may become pregnant should use this medication with caution and only when the benefits of treatment outweigh the risks. Safety in children has not been established, necessitating caution in use. Elderly patients may be at risk for bone complications, hence regular monitoring and consideration of Vitamin D3 administration should be made. Safe dialysis dilution water must be used, at the level of purified water, and care should be taken to avoid risks of dialysis membrane rupture or bleeding. During preparation, do not mix with sodium bicarbonate solution, and ensure the dilution concentration is precisely matched; improper concentrations may result in headaches, blood pressure abnormalities, and consciousness disorders. The electrolyte concentration and pH of the dialysis solution must be confirmed before use, and it should be used immediately after dilution. The usage temperature should be maintained around body temperature, and it should not be used for injection or peritoneal perfusion.

Side effects and when to seek care immediately

Serious side effects

  • Clouding of consciousness
  • convulsions
  • consciousness disorders

Mild side effects

  • Hypoglycemia
  • hyperglycemia
  • weight gain
  • tendency to increase blood pressure
  • osteoporosis
  • osteomalacia
  • fibrous osteitis
  • ectopic calcification
  • headache
  • nausea
Show 16 more
  • vomiting
  • convulsions
  • clouding of consciousness
  • malaise
  • fatigue
  • hypotension
  • shock symptoms
  • increased blood pressure
  • headache
  • palpitations
  • consciousness disorders
  • feelings of limb paralysis
  • general fatigue
  • chest discomfort
  • sudden drops in blood pressure
  • consciousness disorders

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

Storage

This medication should be stored in a sealed container to protect it from air exposure, preferably at room temperature. It is safer to avoid extremely hot or cold places and keep it in a cool area out of direct sunlight.

Appearance and packaging

Appearance

Colorless and transparent liquid filled in a plastic container

Package unit

5.5L, 10L

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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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.