Medication info

C-Vita Injection (Ascorbic Acid)

Prescription medication정맥Expired
Ingredient · strength
Ascorbic Acid›500mg / 1mL
Manufacturer / importer
(주)텔콘알에프제약
Appearance
A brown vial containing a clear colorless or pale yellow injection solution
Packaging
20mL, 25mL, 30mL, 40mL, 50mL x 10 vials
Approval status
Expired

MFDS item code 201901125 · Notified 2019.02.22

This product's status changed to Expired on 2024.02.22. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Prevention of vitamin C deficiency, treatment of scurvy, and promotion of capillary bleeding and bone healing effects
Who receives it
Adults
Adult administration
As ascorbic acid, it is administered subcutaneously, intramuscularly, or intravenously 1 time per day to several times per day, at a dose of 50-1,000 mg daily. Adjust according to age and symptoms.

Ingredients

Manufacturer
(주)텔콘알에프제약

Efficacy & effects

Prevention of vitamin C deficiency, treatment of scurvy, and promotion of capillary bleeding and bone healing effects

  • Scurvy
  • capillary bleeding
  • epistaxis
  • gingival bleeding
  • hematuria
  • melasma
  • freckles
  • post-inflammatory pigmentation
  • photosensitive dermatitis
View approved original text

This medication is used for the prevention and treatment of acute vitamin C deficiency diseases such as scurvy. It is also effective in situations where the demand for vitamin C increases, such as in pregnant and nursing women or individuals engaged in intense physical labor. It helps with capillary bleeding associated with vitamin C deficiency or metabolic disorders, alleviates side effects from drug administration, and promotes bone formation and healing in case of fractures. It is also used for skin-related symptoms like melasma, freckles, post-inflammatory hyperpigmentation, and photosensitive dermatitis. It is a useful aid in improving vitamin C deficiency issues in a variety of situations.

How it is given

Adult administration

As ascorbic acid, it is administered subcutaneously, intramuscularly, or intravenously 1 time per day to several times per day, at a dose of 50-1,000 mg daily. Adjust according to age and symptoms.

Precautions

This medication may cause adverse reactions due to glass fragments when using ampule injections; therefore, great care should be taken when cutting the container. Extra caution should be exercised when administering to children or the elderly. It contains sodium bisulfite, which may cause allergic reactions, and there is a risk of severe asthma attacks in asthmatic patients. Patients with hypersensitivity to this medication, as well as those with hyperoxaluria, Mediterranean anemia, gout, cystinuria, G6PD deficiency, and those with kidney stones should not use this medication. While taking this medication, symptoms like nausea, vomiting, diarrhea, abdominal pain, fatigue, headache, and insomnia may occur, and high doses may lead to kidney stones or diuretic effects. Excessive dosing can cause the drug to precipitate in the urinary tract, leading to stones, so the prescribed dosage must be adhered to. Although this medication is usually taken orally, it should only be given as an injection if oral administration is not feasible, and it is best to switch to oral administration as soon as possible. It may interact with other medications, so caution is advised when taken with salicylates, aspirin, iron supplements, anticonvulsants, oral contraceptives, and some antibiotics. During pregnancy, the effects on the fetus are not clearly understood, so it should be administered only if absolutely necessary and high doses should be avoided. This medication may affect test results, so caution is required when interpreting results of urine glucose tests or blood urine tests. Overdosing may lead to diarrhea or kidney stones, so treatment should be sought immediately if symptoms occur. When used as an injection, there may be pain at the injection site, and more care should be taken when administering to newborns or children. If pain or blood reflux is felt during injection, the needle should be removed immediately, and intravenous administration should be performed slowly to prevent dizziness or venous pain. This medication should be kept out of reach of children, stored away from direct sunlight, and kept in a dry place. It is also important not to transfer the medication from its original container to another, and to keep it properly closed in the original container.

Side effects and when to seek care immediately

Serious side effects

Severe allergic reactions such as sulfite anaphylaxis, asthma attacks, hemolysis in G6PD deficient patients

Mild side effects

Nausea, vomiting, diarrhea, heartburn, abdominal cramps, fatigue, flushing, headache, insomnia, temporary mild pain at the injection site, dizziness, venous pain

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

Storage

This medication is sensitive to light and should be stored in an opaque container. Additionally, it is important to store it at refrigerator temperatures between 2 degrees and 8 degrees Celsius to maintain its freshness.

Appearance and packaging

Appearance

A brown vial containing a clear colorless or pale yellow injection solution

Package unit

20mL, 25mL, 30mL, 40mL, 50mL x 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.

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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.