Netherlands· NL-659b64046636
Vectibix, concentraat voor oplossing voor infusie
A panitumumab product containing panitumumab, registered in Netherlands by Amgen Europe B.V.. The same ATC class is registered in 13 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
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: Netherlands, from CBG-MEB (Netherlands)
- 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
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- PANITUMUMAB
- Manufacturer
- Amgen Europe B.V.
- Country
- Netherlands (NL)
- ATC code
- L01FE02
- ATC class
- Panitumumab
- Defined daily dose
- 30 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/07/423
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.
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.
- United StatesVectibixAmgen, Inc
- BelgiumVectibix 20 mg/mlAmgen Europe
- SpainVECTIBIX 20 mg/ml CONCENTRADO PARA SOLUCION PARA PERFUSIONAmgen Europe B.V.
- CzechiaVECTIBIXAmgen Europe B.V., Breda
- CanadaVECTIBIXAMGEN CANADA INC
- FinlandVectibixAmgen Europe B.V.
- United KingdomVectibix 100mg/5ml concentrate for solution for infusion vialsAmgen Ltd
- Japanパニツムマブ(遺伝子組換え)武田薬品工業
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 CBG-MEB (Netherlands). 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/e2f438d6-7f55-4c7d-9700-80b3df2bad99 GET /v1/drugs/e2f438d6-7f55-4c7d-9700-80b3df2bad99?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": "Concentraat voor oplossing voor infusie",
"route": null,
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/vectibix-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Panitumumab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp73254",
"excipients": [
"AZIJNZUUR (E 260)",
"NATRIUMACETAAT 3-WATER (E 262)",
"NATRIUMCHLORIDE",
"WATER VOOR INJECTIE"
],
"substances": [
"PANITUMUMAB"
],
"leaflet_url": null,
"authorised_at": "2007/12/03",
"procedure_number": "EMEA/H/C/000741",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/07/423",
"additional_monitoring": "N"
}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.