Cholecalciferol Injection 300,000 IU
Cholecalciferol 7.5mg
Injections · Prescription medication
Heuons Co., Ltd.
MFDS item code 201600527 · Notified 2016.01.26
Prevention and treatment of vitamin D deficiency due to malabsorption
This medication is used to prevent and treat vitamin D deficiency in adults at high risk of deficiency due to malabsorption.
Use as prescribed by a physician, adjusting the dosage based on the level of 25-hydroxy vitamin D in the blood. Adults are to be given 300,000 IU of cholecalciferol by intramuscular injection. The annual dosage should not exceed 600,000 IU of cholecalciferol.
This medication is an injectable supplement of vitamin D that helps maintain the balance of calcium and phosphorus in the body. When used with vitamin D fortified foods or other vitamin D preparations, the total intake of vitamin D should be carefully calculated. Regularly check calcium levels in blood and urine; if calcium levels exceed the normal range, administration should be discontinued. Particularly careful measures should be taken when opening the ampoule to prevent glass fragments from mixing, especially for children or elderly individuals. It is generally safe not to use this medication for individuals with certain diseases or those who are pregnant or breastfeeding. Side effects such as headaches, fatigue, muscle pain, digestive disorders, dehydration, high blood pressure, and kidney problems may occur during intake. If unusual symptoms appear, consult a healthcare professional immediately. Blood vitamin D levels and parathyroid hormone levels should be periodically monitored, and patients with reduced kidney function or those taking certain medications should be closely observed. There may be interactions with other medications, so it is important to inform the healthcare provider of any medications being taken. In case of overdose, administration should be immediately stopped, calcium intake should be reduced, ample hydration should be maintained, and dialysis treatment may be necessary if needed. Ampoules should be used immediately after opening, and any remaining medication should be discarded. Store in a cool place, away from direct sunlight.
Headache, weakness, fatigue, muscle pain, loss of appetite, weight loss, growth retardation, nausea, vomiting, constipation, diarrhea, polydipsia, polyuria, dehydration, high blood pressure, calcium stones, tissue calcification in kidneys and blood vessels, kidney disorders, hypercalcemia, arrhythmia, psychological symptoms, sensory disturbances, joint pain, myasthenia, drowsiness, azotemia, hypersensitivity, thirst, confusion, bloating, abdominal pain, metallic taste, dry mouth, rash, itching, hypercalcemia.
Not everyone experiences these, and they can vary from person to person.
This medicine may deteriorate due to air or light, so it should be kept in a sealed container in a place where light does not enter. It is advisable to maintain storage temperatures between 1 degree and 30 degrees Celsius.
A yellowish solution of cholecalciferol ranging from colorless to green contained in brown glass ampoules.
1ml × 10 ampoules
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Injections · Prescription medication
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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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For anything that needs medical judgment, consult a doctor or pharmacist.
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.