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Belgium· BE-AMP-SAM311044-00

Vectibix 20 mg/ml

A panitumumab product containing panitumumab, registered in Belgium by Amgen Europe. The same ATC class is registered in 13 of our 19 countries.

ATC L01FE02

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedVectibix 20 mg/mlATCL01FE02REGISTER NO.BE-AMP-SAM311044-00PACKS LISTED2CHECKEDSeptember 26, 2026

Where it is registered

Panitumumab is registered in 13 of 19 countries.

Countries holding a registration under ATC L01FE02 (panitumumab), each read from that country’s own register.

  • This record: Belgium, from FAMHP / AFMPS (Belgium)
  • 8 of them publish a price we can compare per daily dose

Panitumumab · ATC L01FE02

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.

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Panitumumab
Manufacturer
Amgen Europe
Country
Belgium (BE)
ATC code
L01FE02
ATC class
Panitumumab
Defined daily dose
30 mg, P
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 2

  • be_apb
    0789958
  • be_apb
    2487734

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 FAMHP / AFMPS (Belgium). 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/aa950fa6-fa85-4da3-80fb-da5dd99816cd
GET /v1/drugs/aa950fa6-fa85-4da3-80fb-da5dd99816cd?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",
  "source": "afmps",
  "status": "AUTHORIZED",
  "name_en": "Vectibix 20 mg/ml",
  "name_fr": "Vectibix 20 mg/ml",
  "name_nl": "Vectibix 20 mg/ml",
  "amp_code": "SAM311044-00",
  "strengths": [
    "20.0000"
  ],
  "pack_count": 1,
  "substances": [
    "Panitumumab"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Panitumumab",
  "authorisation_numbers": [
    "EU/1/07/423/003"
  ]
}

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.