Finland· FI-REL-REL48637
Kyntheum
A brodalumab product containing brodalumab, registered in Finland by Leo Pharma A/S. The same ATC class is registered in 13 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Brodalumab is registered in 13 of 19 countries.
Countries holding a registration under ATC L04AC12 (brodalumab), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 8 of them publish a price we can compare per daily dose
Brodalumab · ATC L04AC12
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
Fimea (Finland)- Active substance
- Brodalumab
- Manufacturer
- Leo Pharma A/S
- Country
- Finland (FI)
- ATC code
- L04AC12
- ATC class
- Brodalumab
- Defined daily dose
- 15 mg, P
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
59 interactions on record for brodalumab.
Graded by severity as the source publishes them — 27 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
Brodalumab · interactions on record
59 records
- 27 severe
- 25 moderate
- 7 minor
Most severe, free to view
- CladribineL01BB04severe
- Talimogene laherparepvecL01XL02severe
- Talimogen laherparepvecL01XX51severe
- LeflunomidL04AA13severe
- 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
Brodalumab in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaKYNTHEUMLEO Pharma A/S, Ballerup
- Japanブロダルマブ(遺伝子組換え)協和キリン
- United StatesSiliqBausch Health US LLC
- FranceKYNTHEUM 210 mg, solution injectable en seringue préremplieLEO PHARMA A/S (DANEMARK)
- United KingdomKyntheum 210mg/1.5ml solution for injection pre-filled syringesLEO Pharma
- IrelandKyntheum 210 mg solution for injection in pre-filled syringeLEO Pharma A/S
- BelgiumKyntheum 210 mgLeo Pharma
- NetherlandsKyntheum 210 mg, oplossing voor injectie in voorgevulde spuitAstraZeneca UK Limited
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Kyntheum
- Iceland · Kyntheum
- Liechtenstein · Kyntheum
- Norway · Kyntheum
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 Fimea (Finland). 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/e73f548d-9459-4e35-9e29-5064407b1d21 GET /v1/drugs/e73f548d-9459-4e35-9e29-5064407b1d21?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.
{
"ddd": "15",
"form": "injektioneste, liuos, esitäytetty ruisku",
"route": "Ihon alle",
"ddd_unit": "mg",
"strength": "210 mg",
"atc_label": "brodalumabi",
"ma_number": null,
"auth_status": "Myyntilupa myönnetty",
"eu_ma_number": "EU/1/16/1155/001-002",
"fimea_rel_id": "REL48637",
"authorised_at": "2017-07-17"
}See everything about brodalumab.
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.