Poland· PL-100467410
Cosentyx
A secukinumab product containing secukinumabum, registered in Poland by Novartis Europharm Limited. The same ATC class is registered in 14 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Secukinumab is registered in 14 of 19 countries.
Countries holding a registration under ATC L04AC10 (secukinumab), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 9 of them publish a price we can compare per daily dose
Secukinumab · ATC L04AC10
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of secukinumab costs, country by country.
Normalised to the WHO defined daily dose (10 mg), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Secukinumab · price per daily dose (10 mg)
USD · FX 28 Sept 2026
- CH Switzerland$48.03
The record
At a glance
URPL (Poland)- Active substance
- Secukinumabum
- Manufacturer
- Novartis Europharm Limited
- Country
- Poland (PL)
- ATC code
- L04AC10
- ATC class
- Secukinumab
- Defined daily dose
- 10 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin07613421049416
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
150 interactions on record for secukinumab.
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
Secukinumab · interactions on record
150 records
- 27 severe
- 116 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
Secukinumab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaCOSENTYXNovartis Europharm Limited, Dublin
- BelgiumCosentyx 75 mgNovartis Europharm
- SpainCOSENTYX 75 MG SOLUCION INYECTABLE EN JERINGA PRECARGADANovartis Europharm Limited
- IcelandCosentyxNovartis Europharm Limited*
- NorwayCosentyxNovartis Europharm Limited (1)
- SwedenCosentyx 75 mg Injektionsvätska, lösning i förfylld sprutaNovartis Europharm Limited
- United StatesCOSENTYXNovartis Pharmaceuticals Corporation
- SwitzerlandCosentyx
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Cosentyx
- Liechtenstein · Cosentyx
- Norway · Cosentyx
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 URPL (Poland). 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/7ad861e8-67f2-4d57-83ab-4f0af5a5b20c GET /v1/drugs/7ad861e8-67f2-4d57-83ab-4f0af5a5b20c?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": "Roztwór do wstrzykiwań w ampułko-strzykawce",
"source": "urpl",
"strength": "75 mg",
"packaging": "07613421049416 ¦ Rpz ¦ EU/1/14/980/012 ¦ 144634\n1 amp.-strzyk. 0,5 ml\nRpz ¦ EU/1/14/980/013 ¦ 144635\n3 amp.-strzyk. 0,5 ml opakowanie zbiorcze",
"substance": "Secukinumabum 75 mg",
"common_name": "Secukinumabum",
"pl_product_id": "100467410",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about secukinumab.
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.