Iceland· IS-EU/1/12/794/001
ADCETRIS
A brentuximab vedotin product containing brentuximabum vedotinum inn, registered in Iceland by Takeda Pharma A/S. The same ATC class is registered in 13 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Brentuximab vedotin is registered in 13 of 19 countries.
Countries holding a registration under ATC L01FX05 (brentuximab vedotin), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 8 of them publish a price we can compare per daily dose
Brentuximab vedotin · ATC L01FX05
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of brentuximab vedotin costs, country by country.
Normalised to the WHO defined daily dose (6 mg), the median price runs from $10.73 in Finland to $468.90 in Switzerland — a ×44 gap.
- 2 markets with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Brentuximab vedotin · price per daily dose (6 mg)
USD · FX 28 Sept 2026
- CH Switzerland$468.90
- FI Finland$10.73
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Brentuximabum vedotinum INN
- Manufacturer
- Takeda Pharma A/S
- Country
- Iceland (IS)
- ATC code
- L01FX05
- ATC class
- Brentuximab vedotin
- Defined daily dose
- 6 mg, P
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 1
1 priced- ean1324881 hgl x1 pakkiISK 442583
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
535 interactions on record for brentuximab vedotin.
Graded by severity as the source publishes them — 33 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
Brentuximab vedotin · interactions on record
535 records
- 33 severe
- 502 moderate
Most severe, free to view
- MipomersenC10AX11severe
- LomitapideC10AX12severe
- ClotrimazoleA01AB18moderate
- RolapitantA04AD14moderate
- 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
Brentuximab vedotin in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandADCETRIS2care4 ApS
- SpainADCETRIS 50 mg POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONTakeda Pharma A/S
- United KingdomAdcetris 50mg powder for concentrate for solution for infusion vialsTakeda UK Ltd
- IrelandADCETRIS 50 mg powder for concentrate for solution for infusionTakeda Pharma A/S
- NorwayAdcetrisTakeda Pharma A/S (1)
- PolandAdcetrisTakeda Pharma A/S
- BelgiumAdcetris 50 mgTakeda Pharma
- SwedenADCETRIS 50 mg Pulver till koncentrat till infusionsvätska, lösningTakeda Pharma A/S
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Liechtenstein · Adcetris
- Norway · Adcetris
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 Icelandic Medicines Agency (Iceland). 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/ac7b8685-8c0b-4bbb-af83-40e0302d77f2 GET /v1/drugs/ac7b8685-8c0b-4bbb-af83-40e0302d77f2?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": "Stofn fyrir innrennslisþykkni, lausn",
"source": "lyfjastofnun",
"atc_raw": "L01FX05",
"marketed": true,
"strength": "50 mg",
"ma_number": "EU/1/12/794/001",
"substance": "Brentuximabum vedotinum INN",
"other_info": null,
"legal_status": "(R) Lyfseðilsskylt\r\n(H) Sjúkrahúsmerkt",
"ma_issued_serial": "41207"
}See everything about brentuximab vedotin.
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.