Crysvita
·
- Prescription status not stated
- Muscles, joints and bones
- Active substance
- Burosumab
- Used in
- Muscles, joints and bones
- Made by
- Kyowa Kirin Holdings B.V.
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Crysvita is indicated for the treatment of X-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. Crysvita is indicated for the treatment of FGF23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.
From the official label · 2026-09-30 · European Medicines Agency
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
United StatesNo exact match for this strength and form
SpainNo exact match for this strength and form
FranceNo exact match for this strength and form
CanadaNo exact match for this strength and form
NetherlandsNo exact match for this strength and form
SwitzerlandNo exact match for this strength and form
Details
| Made by | Kyowa Kirin Holdings B.V. |
|---|---|
| Active substance | Burosumab |
| Used in | Muscles, joints and bones |
| Classification | M05BX05 · Muscles, joints and bones |
| Orphan medicine | Yes — designated for a rare disease, according to the register |
| Authorised on | 2018-02-19 |
| Last updated by the regulator | 2026-06-10 |
| EMA product number | EMEA/H/C/004275 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).