Medication info

Deferol Injection (Cholecalciferol)

Prescription medicationInjections근육Approval withdrawn
Ingredient · strength
Cholecalciferol›5mg / 1mL
Manufacturer / importer
(주)경보제약
Appearance
A colorless and transparent injection in a vial, containing a colorless, transparent liquid without odor, of pale yellow color.
Packaging
10 vials
Approval status
Approval withdrawn

MFDS item code 201604985 · Notified 2016.08.17

This product's status changed to Approval withdrawn on 2024.07.08. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Prevention and treatment of vitamin D deficiency
Who receives it
Adults · Children
Adult administration
Administer 200,000 IU of cholecalciferol via intramuscular injection. For the elderly, administer 100,000 IU of cholecalciferol via intramuscular injection. Ensure that the annual dosage does not exceed 600,000 IU of cholecalciferol.
Child administration
Administer 200,000 IU of cholecalciferol via intramuscular injection.

Ingredients

Manufacturer
(주)경보제약

Efficacy & effects

Prevention and treatment of vitamin D deficiency

  • Vitamin D deficiency
View approved original text

This medicine is used to prevent and treat vitamin D deficiency in elderly individuals, adolescents, and adults who are lacking vitamin D. Vitamin D is essential for maintaining bone health and immune function, and thus helps improve issues that may arise due to deficiency. It is effectively used to prevent and treat various health problems that can occur due to vitamin D deficiency.

How it is given

Adult administration

Administer 200,000 IU of cholecalciferol via intramuscular injection. For the elderly, administer 100,000 IU of cholecalciferol via intramuscular injection. Ensure that the annual dosage does not exceed 600,000 IU of cholecalciferol.

Child administration

Administer 200,000 IU of cholecalciferol via intramuscular injection.

Precautions

This medication is a supplement for vitamin D, and when used alongside foods fortified with vitamin D or other treatments, the total amount of vitamin D should be verified. Blood calcium levels should be monitored periodically, and if they exceed normal ranges, the medication should be discontinued. It is important to regularly observe blood and urine calcium levels for individuals with high calcium intake. This medication should not be used by those with specific diseases or by pregnant or breastfeeding individuals. Various side effects, such as headaches, fatigue, myalgia, dyspepsia, dehydration, and hypertension, may occur, so any unusual symptoms should be immediately discussed with a healthcare professional. Particular caution is necessary for individuals with impaired kidney function or limited mobility. During treatment, the levels of vitamin D in the blood and parathyroid hormone should be regularly monitored to maintain the appropriate dosage. Kidney function indicated by creatinine levels should also be monitored regularly, especially in elderly patients or those taking specific medications, requiring more careful observation. There may be interactions with other medications, so consultation with a specialist is necessary when taking antiepileptics, diuretics, antacids, etc. In case of overdose, the medication should be immediately discontinued, calcium intake should be reduced, and fluid intake should be increased. It is safe to use the medication quickly after opening, and any remaining medication should be disposed of properly. When storing the medication, it should be kept in a sealed container to avoid exposure to air and light, and it is best to store it in a cool place between 1 to 25 degrees Celsius, avoiding direct sunlight.

Side effects and when to seek care immediately

Serious side effects

Hypercalcemia, hypercalciuria, calcium stones, kidney dysfunction, ectopic calcification, tissue calcification in kidneys and blood vessels, urticaria.

Mild side effects

  • Headache
  • weakness
  • fatigue
  • myalgia
  • loss of appetite
  • weight loss
  • growth retardation
  • nausea
  • vomiting
  • constipation
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  • diarrhea
  • polyuria
  • dehydration
  • hypertension
  • arrhythmias
  • mental symptoms
  • self-awareness disorders
  • arthralgia
  • myasthenia
  • drowsiness
  • azotemia
  • hypersensitivity
  • thirst
  • confusion
  • abdominal distension
  • abdominal pain
  • metallic taste
  • dry mouth
  • rash
  • itching
  • hyperphosphatemia
  • hyperphosphaturia
  • injection site granuloma
  • injection site nodules
  • injection site reactions
  • injection site pain.

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

Storage

This medication should be stored in a sealed container to avoid exposure to air and light. It is advisable to keep it in a cool place between 1 and 25 degrees Celsius and avoid direct sunlight.

Appearance and packaging

Appearance

A colorless and transparent injection in a vial, containing a colorless, transparent liquid without odor, of pale yellow color.

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.