Medetox Mega Vita D Injection (Cholecalciferol)

Adult dosage

For adults, administer 200,000 IU of cholecalciferol via intramuscular injection. For elderly individuals, administer 100,000 IU of cholecalciferol via intramuscular injection. Do not exceed an annual dosage of 600,000 IU of cholecalciferol.

Children's dosage

For adolescents, administer 200,000 IU of cholecalciferol via intramuscular injection.

Since this medication contains vitamin D, it is important to carefully monitor the total vitamin D intake when taking it with vitamin D-fortified foods or other vitamin D preparations. Regular testing of blood calcium levels is necessary, and if calcium levels become too high, the use of this medication should be discontinued. For those consuming high amounts of calcium, it is important to consistently monitor calcium levels in the blood and urine. This medication should not be taken by individuals with allergies to it or with specific conditions such as hypercalcemia or kidney stones. Patients with impaired kidney function or limited mobility, pregnant women, and nursing mothers should refrain from using this medication for safety reasons. Various side effects such as headaches, fatigue, nausea, vomiting, diarrhea, dehydration, high blood pressure, and kidney issues may occur during treatment; any abnormal symptoms should be promptly discussed with a doctor. It is necessary to regularly monitor blood vitamin D levels and parathyroid hormone levels to maintain the appropriate dosage. Particularly, elderly patients or those taking heart medications and diuretics should frequently check kidney function and may need dosage adjustments or cessation if abnormalities arise. This medication may interact with other drugs; therefore, inform healthcare professionals when taking it alongside anticonvulsants, steroids, certain diuretics, antacids, warfarin, etc. Excessive intake of vitamin D should be avoided during pregnancy, and this medication is not recommended for pregnant or breastfeeding women. The safety and efficacy for children under 12 years have not yet been established; therefore, use should be avoided. In case of overdose, stop taking immediately, reduce calcium intake, drink plenty of water, and supportive treatment to promote diuresis may be needed. Do not mix this medication with others; use promptly after opening and discard any remaining medicine. Store protected from light and at room temperature between 1 to 30 degrees Celsius for optimal efficacy.

Serious side effects

• Hypercalcemia
• hypercalciuria
• kidney impairment
• arrhythmias
• hypersensitivity reactions
• rash
• hives

Mild side effects

Headache, weakness, fatigue, muscle pain, loss of appetite, weight loss, growth retardation, nausea, vomiting, constipation, diarrhea, polydipsia, polyuria, dehydration, hypertension, calcium stones, calcification of tissues such as kidneys and blood vessels, excessive bone calcification, arrhythmia, mental symptoms, perceptual disturbances, joint pain, myasthenia, drowsiness, nitrogenemia, hypersensitivity reactions, thirst, confusion, gas bloating, abdominal pain, metallic taste, dry mouth, rash, itching, hypercalciuria, hypercalcemia,

This medication is sensitive to light, so it should be stored in a container that prevents light exposure. Additionally, it is recommended to store the medication at room temperature between 1 to 30 degrees Celsius to maintain its efficacy.

Appearance

A clear light yellow liquid in a brown glass ampoule injection.

Package unit

5 ampoules/box [1 mL/ampoule X 5], 5 ampoules/box [0.5 mL/ampoule X 5]