Medication info

Olmiere Injection

Prescription medicationInjections정맥
Ingredient · strength
Ascorbic Acid›100mg / 1 vialRetinol Palmitate›1.815mg / 1 vialErgocalciferol›5μg / 1 vialThiamine Hydrochloride›3.81mg / 1 vialRiboflavin Sodium Phosphate›3.6mg / 1 vialPyridoxine Hydrochloride›4.86mg / 1 vialNicotinamide›40mg / 1 vialDexpanthenol›15mg / 1 vialTocopherol Acetate›10mg / 1 vialD-Biotin›60μg / 1 vialFolic Acid›400μg / 1 vialCyanocobalamin›5μg / 1 vial
Manufacturer / importer
삼성제약(주)
Appearance
A freeze-dried injection in a brown vial containing yellow powder
Packaging
10 vials
Approval status
Active

MFDS item code 201601559 · Notified 2016.03.18

Summary

Main use
Maintaining vitamins in patients receiving intravenous nutrition and preventing trauma (surgery, burns) and severe infections
Who receives it
Adults · Children
Adult administration
Dissolve 5 mL of injection-grade distilled water gently and mix within 5 minutes with 500 to 1,000 mL of intravenous glucose injection solution, saline solution, or similar infusion for intravenous use, administered as a drip once daily.
Child administration
Dissolve 5 mL of injection-grade distilled water gently and mix within 5 minutes with 500 to 1,000 mL of intravenous glucose injection solution, saline solution, or similar infusion for intravenous use, administered once daily.

Ingredients

Manufacturer
삼성제약(주)

Efficacy & effects

Maintaining vitamins in patients receiving intravenous nutrition and preventing trauma (surgery, burns) and severe infections

  • Vitamin deficiency
View approved original text

This medication helps maintain vitamins in patients receiving nutrition through intravenous solutions, particularly for preventing vitamin deficiencies in patients with trauma such as surgical patients, severe burns, fractures, and those with severe infections or in a comatose state.

How it is given

Adult administration

Dissolve 5 mL of injection-grade distilled water gently and mix within 5 minutes with 500 to 1,000 mL of intravenous glucose injection solution, saline solution, or similar infusion for intravenous use, administered as a drip once daily.

Child administration

Dissolve 5 mL of injection-grade distilled water gently and mix within 5 minutes with 500 to 1,000 mL of intravenous glucose injection solution, saline solution, or similar infusion for intravenous use, administered once daily.

Precautions

This medication should be used with caution in women during the first 3 months of pregnancy or those who may become pregnant, as vitamin A should not be administered in doses exceeding 5,000 IU per day due to the risk of congenital malformations. Patients with hypersensitivity to any of the components of this medication or hemophilia should not use it. Caution is advised for patients with hypercalcemia, impaired kidney function, children under 11 years old, patients with a history of allergies, and those with a history of drug hypersensitivity. Overdose may lead to hypersensitivity reactions to vitamins A and D or severe allergic reactions such as anaphylaxis, thus symptoms should be closely monitored. If used for more than a few weeks, it is necessary to check for accumulations of vitamins A and D in the body. This medication may interact with certain drugs, so caution is required when used alongside other medications. Pregnant or breastfeeding women should administer it cautiously to avoid side effects due to vitamin overdose. Safety and efficacy in children under 11 years have not been established, so it is advisable to avoid use. Elderly patients may require dosage adjustments due to potentially decreased bodily functions. This medication may affect urine test results, so it should be considered during testing. Unused portions should not be reused, and careful storage should be maintained to avoid light and freezing.

Side effects and when to seek care immediately

Serious side effects

  • Hypotension
  • altered consciousness
  • difficulty breathing
  • shock
  • symptoms of anaphylaxis

Mild side effects

  • Hypotension, altered consciousness, cyanosis, nausea, chest discomfort, facial flushing, itching, sweating
  • Worsening of hypercalcemia, risk of decreased kidney function, dizziness, fainting
  • Influence on clinical test results (interference with urine glucose detection, false negative reactions, yellow discoloration of urine)

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

Storage

This medication should be stored in a sealed container to avoid contact with air and kept at room temperature between 1 to 30 degrees Celsius. Proper storage helps maintain the medication's effectiveness.

Appearance and packaging

Appearance

A freeze-dried injection in a brown vial containing yellow powder

Package unit

10 vials

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.