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Ireland· IE-PA-EU/1/07/423/001-003

Vectibix 20 mg/mL concentrate for solution for infusion

A panitumumab product containing panitumumab, registered in Ireland by Amgen Europe B.V.,. The same ATC class is registered in 2 of our 19 countries.

ATC L01XC08

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedVectibix 20 mg/mL concentrate for sol…ATCL01XC08REGISTER NO.IE-PA-EU/1/07/423/001…PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Panitumumab is registered in 2 of 19 countries.

Countries holding a registration under ATC L01XC08 (panitumumab), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 1 of them publish a price we can compare per daily dose

Panitumumab · ATC L01XC08

2 / 19 countries

  • Belgiumprice
  • Ireland
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

HPRA (Ireland)
Active substance
Panitumumab
Manufacturer
Amgen Europe B.V.,
Country
Ireland (IE)
ATC code
L01XC08
ATC class
Panitumumab
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/07/423/001-003

Regulatory notes

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

Interactions

27 interactions on record for panitumumab.

Graded by severity as the source publishes them — 14 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

Panitumumab · interactions on record

27 records

  • 14 severe
  • 13 moderate

Most severe, free to view

  • AmiodaroneC01BD01severe
  • DofetilideC01BD04severe
  • DronedaroneC01BD07severe
  • IrinotecanL01CE02severe
  • 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

Panitumumab in 15 other countries

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

All panitumumab products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Iceland · Vectibix
  • Norway · Vectibix

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 HPRA (Ireland). 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/e2471ee6-12b6-48b3-ad06-4637cddf3e03
GET /v1/drugs/e2471ee6-12b6-48b3-ad06-4637cddf3e03?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": "Concentrate for solution for infusion",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "L01XC",
    "L01XC08"
  ],
  "strength": null,
  "pa_number": "EU/1/07/423/001-003",
  "substances": [
    "Panitumumab"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": null,
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about panitumumab.

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.