Poland· PL-100249251

Yervoy

A ipilimumab product containing ipilimumabum, registered in Poland by Bristol-Myers Squibb Pharma EEIG. The same ATC class is registered in 13 of our 19 countries.

ATC L01FX04

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedYervoyATCL01FX04REGISTER NO.PL-100249251PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Ipilimumab is registered in 13 of 19 countries.

Countries holding a registration under ATC L01FX04 (ipilimumab), 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

Ipilimumab · ATC L01FX04

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Japan
  • 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 ipilimumab 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

Ipilimumab · price per daily dose (10 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$884.82
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
Ipilimumabum
Manufacturer
Bristol-Myers Squibb Pharma EEIG
Country
Poland (PL)
ATC code
L01FX04
ATC class
Ipilimumab
Defined daily dose
10 mg, P
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909990872442
  • gtin
    05909990872459

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

157 interactions on record for ipilimumab.

Graded by severity as the source publishes them — 25 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

Ipilimumab · interactions on record

157 records

  • 25 severe
  • 132 moderate

Most severe, free to view

  • DicoumarolB01AA01severe
  • WarfarinB01AA03severe
  • HeparinB01AB01severe
  • DalteparinB01AB04severe
  • 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

Ipilimumab in 15 other countries

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

All ipilimumab products

Authorised across Europe · EMA

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

  • Iceland · Yervoy
  • Liechtenstein · Yervoy
  • Norway · Yervoy

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/4c252b57-bdfe-4e9a-ade7-c9ebb559c25f
GET /v1/drugs/4c252b57-bdfe-4e9a-ade7-c9ebb559c25f?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": "Koncentrat do sporządzania roztworu do infuzji",
  "source": "urpl",
  "strength": "5 mg/ml",
  "packaging": "05909990872442 ¦ Rpz ¦ EU/1/11/698/001 ¦ 66855\n1 fiol. 10 ml\n05909990872459 ¦ Rpz ¦ EU/1/11/698/002 ¦ 66856\n1 fiol. 40 ml",
  "substance": "Ipilimumabum 5 mg/ml",
  "common_name": "Ipilimumabum",
  "pl_product_id": "100249251",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about ipilimumab.

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.