Belgium· BE-AMP-SAM533813-00
Ilaris 150 mg/ml
A canakinumab product containing canakinumab, registered in Belgium by Novartis Europharm. The same ATC class is registered in 14 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Canakinumab is registered in 14 of 19 countries.
Countries holding a registration under ATC L04AC08 (canakinumab), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 9 of them publish a price we can compare per daily dose
Canakinumab · ATC L04AC08
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Canakinumab
- Manufacturer
- Novartis Europharm
- Country
- Belgium (BE)
- ATC code
- L04AC08
- ATC class
- Canakinumab
- Defined daily dose
- 2.7 mg, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb7722507
- be_apb3571650
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
374 interactions on record for canakinumab.
Graded by severity as the source publishes them — 30 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Canakinumab · interactions on record
374 records
- 30 severe
- 337 moderate
- 7 minor
Most severe, free to view
- CladribineL01BB04severe
- PrednisoloneA07EA01moderate
- HydrocortisoneA07EA02moderate
- PrednisoneA07EA03moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Canakinumab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandIlaris
- CzechiaILARISNovartis Europharm Limited, Dublin
- SpainILARIS 150 MG/ML SOLUCION INYECTABLENovartis Europharm Limited
- NorwayIlarisNovartis Europharm Limited (1)
- PolandIlarisNovartis Europharm Limited
- SwedenIlaris 150 mg/ml Injektionsvätska, lösningNovartis Europharm Limited
- United KingdomIlaris 150mg powder for solution for injection vialsNovartis Pharmaceuticals UK Ltd
- IcelandIlarisNovartis Europharm Limited*
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Ilaris
- Liechtenstein · Ilaris
- Norway · Ilaris
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FAMHP / AFMPS (Belgium). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/0e138555-5138-4f2b-9a7d-4ab3b116e1d2 GET /v1/drugs/0e138555-5138-4f2b-9a7d-4ab3b116e1d2?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"form": "Solution for injection",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Ilaris 150 mg/ml",
"name_fr": "Ilaris 150 mg/ml",
"name_nl": "Ilaris 150 mg/ml",
"amp_code": "SAM533813-00",
"strengths": [
"150.0000"
],
"pack_count": 1,
"substances": [
"Canakinumab",
"Mannitol",
"Polysorbate 80"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Canakinumab",
"authorisation_numbers": [
"EU/1/09/564/004"
]
}See everything about canakinumab.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.