Belgium· BE-AMP-SAM372197-00

Arzerra 100 mg

A ofatumumab product containing ofatumumab, registered in Belgium by Novartis Europharm. The same ATC class is registered in 2 of our 19 countries.

ATC L01FA02

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedArzerra 100 mgATCL01FA02REGISTER NO.BE-AMP-SAM372197-00PACKS LISTED0CHECKEDSeptember 26, 2026

Where it is registered

Ofatumumab is registered in 2 of 19 countries.

Countries holding a registration under ATC L01FA02 (ofatumumab), each read from that country’s own register.

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

Ofatumumab · ATC L01FA02

2 / 19 countries

  • Belgiumprice
  • Finlandprice
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
Ofatumumab
Manufacturer
Novartis Europharm
Country
Belgium (BE)
ATC code
L01FA02
ATC class
Ofatumumab
Defined daily dose
0.133 g, P
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 0

No packs listed by the register for this record.

Regulatory notes

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

Interactions

70 interactions on record for ofatumumab.

Graded by severity as the source publishes them — 29 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

Ofatumumab · interactions on record

70 records

  • 29 severe
  • 41 moderate

Most severe, free to view

  • CladribineL01BB04severe
  • Talimogene laherparepvecL01XL02severe
  • Talimogen laherparepvecL01XX51severe
  • LeflunomidL04AA13severe
  • 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.

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/d0748be5-9456-444d-9d39-b50ecbd29549
GET /v1/drugs/d0748be5-9456-444d-9d39-b50ecbd29549?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": "REVOKED",
  "name_en": "Arzerra 100 mg",
  "name_fr": "Arzerra 100 mg",
  "name_nl": "Arzerra 100 mg",
  "amp_code": "SAM372197-00",
  "strengths": [
    "20.0000",
    "20.0000"
  ],
  "pack_count": 2,
  "substances": [
    "Ofatumumab"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Ofatumumab",
  "authorisation_numbers": [
    "EU/1/10/625/001",
    "EU/1/10/625/002"
  ]
}

See everything about ofatumumab.

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.