D3 Base Injection 100,000 IU (Cholecalciferol)

Adult administration

Administer according to doctor's prescription, adjusting the dose based on the level of 25-hydroxy Vitamin D in the blood. For the elderly, treatment effectiveness and tolerability should be reviewed within three months to determine whether re-administration is necessary. Administer cholecalciferol 100,000 IU intramuscularly.

This medication contains Vitamin D, so when taking other medications or fortified foods that contain Vitamin D, it is essential to check the total intake of Vitamin D. Regularly monitor calcium levels in the blood and urine; if calcium levels become too high, the medication should be discontinued. If there is a high intake of calcium, it is especially important to observe calcium levels in the blood and urine more frequently. This medication is not recommended for certain patients. For instance, those with allergies to this medication, hypercalcemia, kidney stones, renal dysfunction, immobilized patients, and women who are pregnant or breastfeeding should avoid taking it. Various side effects may occur, such as headaches, muscle pain, gastrointestinal disturbances, dehydration, elevated blood pressure, and kidney issues; therefore, if any unusual symptoms arise, immediate consultation with a healthcare professional is necessary. It is particularly safe to administer while regularly checking the levels of vitamin D and parathyroid hormone in the blood. Patients with reduced renal function or the elderly should frequently monitor their renal status through blood tests and adjust the dosage if necessary. This medication may interact with other drugs, so inform healthcare professionals if taken with anticonvulsants, diuretics, steroids, etc. It is safest for pregnant or breastfeeding women to avoid this medication and to consult a doctor before taking if planning to become pregnant. Safety and efficacy in children have not been sufficiently established, so caution is needed when administering to pediatric patients. In case of overdose, immediately discontinue the medication, reduce calcium intake, and ensure adequate hydration and diuresis to help eliminate calcium. This medication should not be mixed with other drugs, and any remaining medication after opening an ampoule should be discarded promptly. Store in a sealed container to prevent exposure to air or light, and keep at a temperature between 1 to 30 degrees Celsius away from direct sunlight to maintain the medication's effectiveness and safety.

Serious side effects

Rash (severe skin reactions), hypersensitivity (severe allergic reactions), renal impairment (severe edema or urinary abnormalities)

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, renal impairment, excessive bone calcification, arrhythmias, mental symptoms, awareness disorders, joint pain, myasthenia, drowsiness, azotemia, thirst, confusion, bloating, abdominal pain, metallic taste, dry mouth, rash, itching, hypercalciuria,

This medication should be stored in a sealed container to prevent exposure to air and light. It should be kept at room temperature between 1 to 30 degrees Celsius, avoiding direct sunlight. Proper storage will help maintain the medication's effectiveness and safety.

Appearance

A cholecalciferol aqueous solution that is yellowish with colorless to greenish hues, contained in a brown glass ampoule injection.

Package unit

6 ampoules/box