Sweden· SE-20020308000025
Kineret 100 mg Injektionsvätska, lösning
A medicinal product containing anakinra, registered in Sweden by Swedish Orphan Biovitrum AB (publ).
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Anakinra
- Manufacturer
- Swedish Orphan Biovitrum AB (publ)
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- August 27, 2026
Packs & prices · 1
- se_varunummer20020308000025
Regulatory notes
No shortage, Orange Book or US label notes for this record.
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.
- BelgiumKineret 100 mgSwedish Orphan Biovitrum (Publ)
- NorwayKineretSwedish Orphan Biovitrum International AB
- CzechiaKINERETSwedish Orphan Biovitrum AB (publ), Stockholm
- SpainKINERET 100 mg/0,67 ml solucion inyectable en jeringa precargadaSwedish 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
- IrelandKineret 100 mg/0.67 ml solution for injection in pre-filled syringeSwedish Orphan Biovitrum AB
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 Swedish Medical Products Agency (Sweden). 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/d343a01c-e9be-4935-b217-ab64f02ec84f GET /v1/drugs/d343a01c-e9be-4935-b217-ab64f02ec84f?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EMA",
"EPAR"
],
"se_npl_id": "20020308000025",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20020308000025",
"product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/kineret"
}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.