Colecalciferol 1000–2000 units/day
Brand names: InVita D3, Fultium-D3, Thorens (high-dose)
Colecalciferol (vitamin D3) at a maintenance daily dose is used to correct and prevent vitamin D deficiency in chronic kidney disease, supporting bone health as part of CKD-mineral and bone disorder management.
Adult dose
Dose adjustments
Severe renal impairment is a CONTRAINDICATION (§4.3). §4.4: use with caution in patients with impairment of renal function and monitor the effect on calcium and phosphate levels, taking the risk of soft tissue calcification into account; in patients with severe renal insufficiency vitamin D in the form of colecalciferol is not metabolised normally and other forms of vitamin D should be used. Should not be taken by patients with a tendency to form calcium-containing renal calculi. Patients with renal disease are also listed in §4.2 as being at high risk of vitamin D deficiency and as possibly requiring higher doses with 25(OH)D monitoring — no numeric higher dose is given. No numeric eGFR-banded dose adjustment is stated in this SPC.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance (colecalciferol) or to any of the excipients
- Hypercalcaemia and/or hypercalciuria
- Nephrolithiasis (renal calculi)
- Hypervitaminosis
- Severe renal impairment
Side effects
- Metabolism and nutrition disorders: hypercalcaemia; hypercalciuria
- Skin and subcutaneous disorders: pruritus; rash; urticaria
- The §4.8 table gives the frequency categories 'uncommon' (less than 1 in 100 people) and 'rare' (less than 1 in 1 000 people), but the column alignment was not preserved in the retrieved text, so individual reactions have not been assigned a frequency here
Interactions
- Cardiac glycosides — patients treated with cardiac glycosides may be susceptible to high calcium levels and should have ECG parameters and calcium levels monitored; reduce the dose or interrupt treatment if urinary calcium exceeds 7.5 mmol/24 hours (300 mg/24 hours) (§4.5)
- Benzothiadiazine derivatives (thiazide diuretics) — increase the risk of hypercalcaemia because they decrease urinary calcium excretion; monitor plasma and urine calcium in patients on long-term treatment (§4.5)
- Metabolites or analogues of vitamin D — careful monitoring of serum calcium is recommended if combined with colecalciferol (§4.5)
- Anticonvulsants (e.g. phenytoin, phenobarbital, primidone) and rifampicin — may diminish the effect of colecalciferol due to hepatic enzyme induction; isoniazid may reduce effectiveness by inhibiting metabolic activation (§4.5)
- Drugs leading to fat malabsorption (e.g. orlistat, liquid paraffin, cholestyramine) — may impair absorption of colecalciferol (§4.5)
- Actinomycin and imidazole antifungal agents — interfere with vitamin D activity by inhibiting conversion (the §4.5 entry was truncated at the source-fetch limit; check the full SPC)
- Phosphate infusions should not be administered to lower the hypercalcaemia of hypervitaminosis D because of the danger of metastatic calcification (§4.5)
Clinical monograph
How it works
Colecalciferol is converted in the liver to 25-hydroxyvitamin D and then in the kidney to active 1,25-dihydroxyvitamin D, which promotes intestinal calcium and phosphate absorption and supports bone mineralisation.
Prescribing in practice
- In advanced CKD renal activation of vitamin D is impaired, so colecalciferol replenishes nutritional stores but an active vitamin D analogue (e.g. alfacalcidol) may be needed for the endocrine effect; avoid in hypercalcaemia.
- Excessive intake causes hypercalcaemia and hyperphosphataemia, which is hazardous in CKD and can worsen vascular calcification.
- Many combination products contain calcium; the plain colecalciferol-only preparation avoids an additional calcium load in patients already on calcium-based binders.
Monitoring
Monitor serum calcium and phosphate, with vitamin D and parathyroid hormone levels as part of CKD-MBD review.
Counselling the patient
- This replaces vitamin D to support your bones; take it regularly as prescribed.
- Do not take additional high-dose vitamin D or calcium supplements without advice.
- Report symptoms of high calcium such as thirst, frequent urination, nausea or confusion.
Evidence & guidelines
Correcting vitamin D deficiency is recommended within CKD-MBD guidance (NICE/KDIGO), with active vitamin D reserved for treating secondary hyperparathyroidism.
Reference: KDIGO CKD-MBD Guidelines 2017; NICE NG203; NICE CG71 (Vitamin D deficiency); Confirm identity and dosing against the manufacturer SPC (eMC) and NICE. Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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- Rhabdomyolysis · Renal Association 2018; UpToDate 2024
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- Hepatorenal Syndrome · EASL 2018; ICA 2015
- Acute Kidney Injury (AKI) · KDIGO 2012 / NICE AKI 2019