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Sunny D Insta injection is a high-dose Vitamin D3 (cholecalciferol) formulation used to treat or prevent vitamin D deficiency, especially when oral administration is not feasible or in cases of malabsorption. Each 1 ml ampoule contains 5 mg (200,000 IU) of Vitamin D3.
Active ingredient: Cholecalciferol (Vitamin D3), 5 mg per 1 ml ampoule (~200,000 IU)
Inactive / excipients: (manufacturer’s formulation including solvent, stabilizers, etc.) — check official leaflet.
Vitamin D analog / Nutritional supplement / Fat-soluble vitamin
Injection (sterile solution) — 1 ml ampoule containing 5 mg cholecalciferol (Vitamin D3)
Sunny D Insta is used for:
Correction of Vitamin D deficiency, especially in patients who cannot take oral supplements
Cases of malabsorption, chronic liver disease, or when oral uptake is compromised
Support for bone health, calcium metabolism, and maintenance of normal vitamin D levels
The dose is high (5 mg / 200,000 IU) in a single ampoule; the exact regimen or frequency is determined by the physician based on the patient’s deficiency severity, baseline vitamin D levels, and risk factors.
Such high-dose injections are typically not repeated frequently; follow monitoring guidelines (e.g. checking serum 25(OH)D, calcium) before further dosing.
Excessive vitamin D can lead to hypercalcemia — symptoms may include nausea, vomiting, weakness, frequent urination, kidney stones, confusion.
Management: Stop supplementation, restrict dietary calcium, hydrate, monitor and treat hypercalcemia under medical supervision.
In a clinical setting, missing an injection should be addressed by the treating physician.
Do not self-administer or double the dose to compensate.
Administer via intramuscular (IM) injection (often recommended for depot effect) or as per manufacturer instructions.
Use aseptic technique.
Monitor patients during and after injection for adverse events, especially in cases of underlying conditions (kidney, calcium metabolism).
Hypercalcemia or hypervitaminosis D
Severe renal impairment or nephrolithiasis
Known hypersensitivity to vitamin D or any component of formulation
Disorders of calcium metabolism (unless under careful monitoring)
Use with caution in pregnancy or lactation — only if clearly needed
Common / Less serious:
Mild hypercalcemia symptoms (thirst, urination)
Gastrointestinal discomfort
Headache
Less common / Serious:
Hypercalcemia and associated complications (renal stones, bone pain)
Soft tissue calcification
Allergic reactions
Monitor serum calcium, phosphate, magnesium after injection
Check renal function
Avoid excessive concurrent intake of calcium or vitamin D
Be cautious in patients with cardiovascular disease, kidney disease, or predisposition to hypercalcemia
Adjust or avoid in patients using thiazide diuretics (which can increase calcium reabsorption)
Thiazide diuretics — may potentiate hypercalcemia
Digoxin — altered calcium levels may affect cardiac rhythm
Magnesium supplements, calcium supplements — risk of additive hypercalcemia
Some anticonvulsants (e.g. phenobarbital, phenytoin) — may increase vitamin D metabolism
Store at controlled room temperature, away from light, heat, and moisture (often ≤ 30 °C)
Do not freeze
Use before expiration
Dispose unused ampoules according to medical waste regulations
Not a controlled substance; it is a prescription / professional-use medication
High-dose injections are tools for repletion, not for frequent long-term use
Always monitor calcium, vitamin D levels, and kidney function post-administration
Avoid combining with high calcium supplements immediately
Be alert for symptoms of hypercalcemia
Use under medical supervision, particularly in patients with comorbid conditions
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