GVS assessment of calcifediol (Hidroferol®)

Zorginstituut Nederland has completed its assessment whether calcifediol (Hidroferol®) is interchangeable with a medicine already included in the Medicine Reimbursement System (GVS). Calcifediol (Hidroferol®) is indicated for treating vitamin D deficiency in adults. The Zorginstituut recommends including calcifediol in List 1A of the Health Insurance Regulation in the 0A11CCBO V cluster.

Registered indication

Calcifediol is licensed for treating vitamin D deficiency in adults, in cases where the initial administration of high doses is required or where staggered administration over time is preferred, such as in the following situations:

  • as an adjuvant for treating osteoporosis;
  • in patients with malabsorption syndrome;
  • renal osteodystrophy;
  • bone disorders induced by treatment with corticosteroid medicinal products.

The recommended dose is one capsule (0.266 mg calcifediol, equivalent to 15,960 IU vitamin D) once a month.

Review of interchangeability

The Zorginstituut carried out a marginal assessment. Based on the criteria for interchangeability, the Zorginstituut has concluded that calcifediol (Hidroferol®) is interchangeable with the other medicinal products in the GVS cluster 0A11CCBO V, which includes various products containing colecalciferol.

Zorginstiuut's advice

Calcifediol (Hidroferol®) can be put in List 1A in the 0A11CCBO V cluster. The standard dose for calcifediol can be set at 8.7 micrograms.

This report is a summary of recommendations by Zorginstituut Nederland. The original text is in Dutch.