Drug Database
Back to search

Poland· PL-100285152

Adcetris

A brentuximab vedotin product containing brentuximabum vedotinum, registered in Poland by Takeda Pharma A/S. The same ATC class is registered in 13 of our 19 countries.

ATC L01FX05

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedAdcetrisATCL01FX05REGISTER NO.PL-100285152PACKS LISTED2CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about brentuximabum vedotinumAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

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: Poland, from URPL (Poland)
  • 8 of them publish a price we can compare per daily dose
Search brentuximab vedotin products by name

Brentuximab vedotin · ATC L01FX05

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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.

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
Open the full comparison — free accountDrug prices for market access

Brentuximab vedotin · price per daily dose (6 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$468.90
  • FI Finland$10.73
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

URPL (Poland)
Active substance
Brentuximabum vedotinum
Manufacturer
Takeda Pharma A/S
Country
Poland (PL)
ATC code
L01FX05
ATC class
Brentuximab vedotin
Defined daily dose
6 mg, P
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909991004545
  • gtin
    07038319114852

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
Check brentuximab vedotin against other medicinesHow interaction checks work

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.
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

Brentuximab vedotin in 15 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All brentuximab vedotin products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Adcetris
  • 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 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/771a9c61-32a5-4444-8af9-0a4fd4e00f31
GET /v1/drugs/771a9c61-32a5-4444-8af9-0a4fd4e00f31?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": "Proszek do sporządzania koncentratu roztworu do infuzji",
  "source": "urpl",
  "strength": "50 mg",
  "packaging": "05909991004545 ¦ Rpz ¦ EU/1/12/794/001 ¦ 78857\n1 fiol. 50 mg proszku\n07038319114852 ¦ Rpz ¦ Skasowane ¦ EU/1/12/794/00 ¦ 130031\n1 fiol.  proszku",
  "substance": "Brentuximabum vedotini 50 mg",
  "common_name": "Brentuximabum vedotinum",
  "pl_product_id": "100285152",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}
API referenceMCP serverPlans

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.

Try it freeOpen in the console