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Vitamin D Supplement (Native Vitamin D3) Pregnancy: Should not be used during pregnancy unless the clinical condition of the woman requires treatment with colecalciferol, at a dose necessary to overcome the deficiency; during pregnancy women should follow the advice of their medical practitioner as requirements vary with the severity of the disease and the response to treatment. Based on human experience and animal studies, vitamin D OVERDOSE causes physical and mental disability and congenital heart and eye conditions, due to hypercalcaemia, when administered during pregnancy. Breast-feeding: colecalciferol and its metabolites are excreted in breast milk; overdose in infants induced by nursing mothers has not been observed, but when prescribing additional vitamin D to a breast-fed child the practitioner should consider the dose of any additional vitamin D given to the mother.

Colecalciferol 1000–2000 units/day

Brand names: InVita D3, Fultium-D3, Thorens (high-dose)

Used in: Falls & Frailty

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.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Prevention of vitamin D deficiency or treatment of vitamin D insufficiency: 1-2 capsules (1 000-2 000 IU) daily
Route: Oral
Frequency: Once daily
Source: UK SPC (eMC) for Colecalciferol 1 000 IU Capsules, §4.2 (https://www.medicines.org.uk/emc/product/7247/smpc). One capsule contains 1 000 IU colecalciferol (vitamin D3); the dose above is the 1 000-2 000 IU/day regimen this page is named for. OTHER ADULT REGIMENS IN §4.2: treatment of vitamin D deficiency — 1-4 capsules (1 000-4 000 IU) daily for 10 weeks depending on the severity of the disease and the patient's response, followed by maintenance therapy of 1-2 capsules (1 000-2 000 IU) daily; follow-up serum 25(OH)D should be measured approximately three to four months after starting maintenance therapy to confirm the target level has been achieved. As an adjunct to specific therapy for osteoporosis — 1 capsule (1 000 IU) daily. HIGHER DOSES MAY BE REQUIRED, with monitoring of serum 25(OH)D, in populations at high risk of deficiency, which the SPC lists as: institutionalised or hospitalised individuals; dark skinned individuals; individuals with limited effective sun exposure due to protective clothing or consistent sunscreen use; patients being evaluated for osteoporosis; obese individuals; use of certain concomitant medicines (e.g. anticonvulsants, glucocorticoids, anti-retrovirals); those recently treated for vitamin D deficiency and requiring maintenance therapy; PATIENTS WITH LIVER OR RENAL DISEASE; and patients with malabsorption including inflammatory bowel disease and coeliac disease. The SPC does not give numeric higher doses for these groups. RENAL CAUTION (critical for this page): §4.3 lists SEVERE RENAL IMPAIRMENT as a contraindication, and §4.4 states that 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; in renal impairment generally, use with caution and monitor the effect on calcium and phosphate levels, taking the risk of soft tissue calcification into account. Should not be taken by patients with a tendency to form calcium-containing renal calculi. Medical supervision is required whilst on treatment to prevent hypercalcaemia; allowance must be made for other vitamin D supplements, vitamin D containing medicines or other sources, and the need for additional calcium supplementation considered for individual patients (calcium supplements to be given under close medical supervision). Caution in patients receiving treatment for cardiovascular disease (cardiac glycosides including digitalis) and in sarcoidosis (risk of increased metabolism of vitamin D to its active form — monitor serum and urine calcium). PAEDIATRIC/ADOLESCENT (no per-kg dose is stated, so paedDose is null): over 12 years, for treatment of vitamin D deficiency or insufficiency, 1 capsule (1 000 IU) daily depending on the severity of the disease and the patient's response, to be given only under medical supervision. NOT RECOMMENDED for infants and children under 12 years. Verify any paediatric use against a children's formulary. METHOD: taken orally; the capsule should be swallowed whole with water, preferably with the main meal of the day. NOTE ON SOURCES: this SPC is for a 1 000 IU capsule product — other colecalciferol products have different strengths and their own posology. §4.5 (interactions) was captured only as an appendix to the §4.4 text in this bundle and was truncated at the fetch limit; §4.5 must be checked in full on the SPC.

Dose adjustments

Renal

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.