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.

ATC L04AC12

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedKyntheumATCL04AC12REGISTER NO.FI-REL-REL48637PACKS LISTED0CHECKEDSeptember 27, 2026

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
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

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.

All brodalumab products

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.