Netherlands· NL-4a11648fc13a
Kineret 100 mg/0,67 ml/ (150 mg/ml), oplossing voor injectie
A anakinra product containing anakinra, registered in Netherlands by Amgen Europe B.V.. The same ATC class is registered in 13 of our 19 countries.
Checked against CBG-MEB (Netherlands) 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: Netherlands, from CBG-MEB (Netherlands)
- 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
CBG-MEB (Netherlands)- Active substance
- ANAKINRA
- Manufacturer
- Amgen Europe B.V.
- Country
- Netherlands (NL)
- ATC code
- L04AC03
- ATC class
- Anakinra
- Defined daily dose
- 0.1 g, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/02/203
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.
- FranceKINERET 100 mg/0,67 mL, solution injectable en seringue préremplieSWEDISH ORPHAN BIOVITRUM INTERNATIONAL (SUEDE)
- IrelandKineret 100 mg/0.67 ml solution for injection in pre-filled syringeSwedish Orphan Biovitrum AB
- United StatesKineretSwedish Orphan Biovitrum AB (publ)
- CzechiaKINERETSwedish Orphan Biovitrum AB (publ), Stockholm
- SwedenKineret 100 mg Injektionsvätska, lösningSwedish Orphan Biovitrum AB (publ)
- BelgiumKineret 100 mgSwedish Orphan Biovitrum (Publ)
- FinlandKineretSwedish Orphan Biovitrum AB (publ)
- 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 CBG-MEB (Netherlands). 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/e8463f18-98f5-47fa-9737-6ea0b5987674 GET /v1/drugs/e8463f18-98f5-47fa-9737-6ea0b5987674?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": "Oplossing voor injectie",
"route": "Subcutaan gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/kineret-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Anakinra",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp71080",
"excipients": [
"CITROENZUUR 0-WATER (E 330)",
"DINATRIUMEDETAAT 2-WATER",
"NATRIUMCHLORIDE",
"NATRIUMHYDROXIDE (E 524)",
"POLYSORBAAT 80 (E 433)",
"WATER VOOR INJECTIE"
],
"substances": [
"ANAKINRA"
],
"leaflet_url": null,
"authorised_at": "2002/03/08",
"procedure_number": "EMEA/H/C/000363",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/02/203",
"additional_monitoring": "N"
}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.