Multivitamin Injection

Adult administration

Dissolve 5 mL of this medication in injectable distilled water, mix gently, and administer intravenously in 500–1,000 mL of dextrose injection, normal saline injection, or a similar intravenous fluid once daily via drip infusion.

Child administration

For children over 11 years old, dissolve 5 mL of this medication in injectable distilled water, mix gently, and then administer intravenously in 500–1,000 mL of dextrose injection, normal saline injection, or a similar intravenous fluid within 5 minutes.

Caution should be taken when administering more than 5,000 IU of vitamin A daily to women in the first three months of pregnancy or those who may become pregnant, as it may pose a risk of congenital malformations in the fetus. This medication should not be used in individuals with hypersensitivity to any of its components or in patients with hemophilia. Patients with hypercalcemia may experience worsened symptoms due to the vitamin D included in this medication, so testing of blood and urine should be conducted to confirm their condition before administering. Patients with impaired renal function should be cautious as excessive doses of vitamin D may elevate calcium levels, further deteriorating kidney function. It is not recommended for children under 11 years of age as safety and efficacy have not been established. Patients with a history of bronchial asthma or skin allergies, as well as individuals with a history of drug hypersensitivity, should be administered this medication with caution. In case of overdose, allergic reactions to vitamins A and D may occur, and in severe cases, symptoms of shock or anaphylaxis may develop, so symptoms should be closely monitored. If adverse reactions occur, administration should be immediately discontinued, and appropriate treatment should be sought. When taken for weeks or more, tests should be conducted to check for accumulation of vitamins A and D in the body. When taken with other medications, interactions may occur, so special caution should be taken with combinations particularly with Acetazolamide, Chlorothiazide Sodium, Tetracycline Hydrochloride, calcium salts, Vitamin K, Levodopa, etc. Pregnant or lactating women should consult with a healthcare professional before taking this medication to avoid the risk of side effects due to vitamin overdose. Elderly patients may have decreased physical function, so dosages should be adjusted or used with caution. This medication may affect clinical test results by interfering with glucose detection in urine and showing false-negative results, and may change the color of urine to yellow. Use immediately after opening, do not reuse remaining medication, and store protected from light. Injecting the undiluted concentrate directly may cause dizziness or fainting, so it must be diluted before use, and the injection solution should be used within 8 hours after mixing. Store out of reach of children, avoid freezing, and keep refrigerated in the original container.

Serious side effects

• Shock
• anaphylactic symptoms
• respiratory distress

Mild side effects

• Itching
• sweating
• hypotension
• altered consciousness
• nausea
• chest discomfort
• facial flushing
• dizziness
• fainting

This medication should be stored in a sealed container, at room temperature between 1 and 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the drug.

Appearance

Lyophilized injection in a brown vial containing yellow powder.

Package unit

5 vials/box, 10 vials/box, 100 vials/box