Belgium· BE-AMP-SAM474622-00
Kineret 100 mg/0.67 ml
A anakinra product containing anakinra, registered in Belgium by Swedish Orphan Biovitrum (Publ). The same ATC class is registered in 13 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Anakinra is registered in 13 of 19 countries.
Countries holding a registration under ATC L04AC03 (anakinra), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 8 of them publish a price we can compare per daily dose
Anakinra · ATC L04AC03
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Anakinra
- Manufacturer
- Swedish Orphan Biovitrum (Publ)
- Country
- Belgium (BE)
- ATC code
- L04AC03
- ATC class
- Anakinra
- Defined daily dose
- 0.1 g, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb3225281
- be_apb7720287
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
375 interactions on record for anakinra.
Graded by severity as the source publishes them — 31 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
Anakinra · interactions on record
375 records
- 31 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
Anakinra in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaKINERETSwedish Orphan Biovitrum AB (publ), Stockholm
- SpainKINERET 100 mg/0,67 ml solucion inyectable en jeringa precargadaSwedish Orphan Biovitrum Ab (Publ)
- IcelandKineret*Swedish Orphan Biovitrum AB (publ)
- PolandKineretSwedish Orphan Biovitrum AB
- SwedenKineret 100 mg/0,67 ml Injektionsvätska, lösning i förfylld sprutaSwedish Orphan Biovitrum AB (publ)
- FinlandKineretSwedish Orphan Biovitrum AB (publ)
- FranceKINERET 100 mg/0,67 mL, solution injectable en seringue préremplieSWEDISH ORPHAN BIOVITRUM INTERNATIONAL (SUEDE)
- United KingdomKineret 100mg/0.67ml solution for injection pre-filled syringesSwedish Orphan Biovitrum Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Kineret
- Liechtenstein · Kineret
- Norway · Kineret
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/1ff3e813-b5ac-4a10-98f6-952d0455404e GET /v1/drugs/1ff3e813-b5ac-4a10-98f6-952d0455404e?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": "Kineret 100 mg/0.67 ml",
"name_fr": "Kineret 100 mg/0.67 ml",
"name_nl": "Kineret 100 mg/0.67 ml",
"amp_code": "SAM474622-00",
"strengths": [
"150.0000"
],
"pack_count": 3,
"substances": [
"Anakinra",
"Disodium Edetate Dihydrate",
"Sodium Chloride",
"Sodium Hydroxide",
"Polysorbate 80"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Anakinra",
"authorisation_numbers": [
"EU/1/02/203/005",
"EU/1/02/203/006",
"EU/1/02/203/007"
]
}See everything about anakinra.
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.