Belgium· BE-AMP-SAM529937-00
Mylotarg 5 mg
A gemtuzumab ozogamicin product containing gemtuzumab ozogamicin, registered in Belgium by Pfizer Europe MA. The same ATC class is registered in 12 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Gemtuzumab ozogamicin is registered in 12 of 19 countries.
Countries holding a registration under ATC L01FX02 (gemtuzumab ozogamicin), 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
Gemtuzumab ozogamicin · ATC L01FX02
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Gemtuzumab Ozogamicin
- Manufacturer
- Pfizer Europe MA
- Country
- Belgium (BE)
- ATC code
- L01FX02
- ATC class
- Gemtuzumab ozogamicin
- Defined daily dose
- 2.1 mg, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 2
- be_apb7724925
- be_apb2446870
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
112 interactions on record for gemtuzumab ozogamicin.
Graded by severity as the source publishes them — 33 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
Gemtuzumab ozogamicin · interactions on record
112 records
- 33 severe
- 64 moderate
- 15 minor
Most severe, free to view
- MipomersenC10AX11severe
- LomitapideC10AX12severe
- CladribineL01BB04severe
- PexidartinibL01EX15severe
- 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
Gemtuzumab ozogamicin in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandMylotarg 5 mg, Pulver für ein Konzentrat zur Herstellung einer InfusionslösungPfizer AG
- CzechiaMYLOTARGPfizer Europe MA EEIG, Bruxelles
- SpainMYLOTARG 5 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONPfizer Europe Ma Eeig
- FinlandMYLOTARGPfizer Europe MA EEIG
- United KingdomMylotarg 5mg powder for concentrate for solution for infusion vialsPfizer Ltd
- IrelandMYLOTARG 5 mg powder for concentrate for solution for infusionPfizer Europe MA EEIG
- IcelandMylotargPfizer Europe MA EEIG*
- NorwayMylotargPfizer Europe MA EEIG (1)
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Mylotarg
- Liechtenstein · Mylotarg
- Norway · Mylotarg
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/d08d0ce3-3e4e-4066-bde4-2c8c2d434be0 GET /v1/drugs/d08d0ce3-3e4e-4066-bde4-2c8c2d434be0?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": "Powder for concentrate for solution for infusion",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Mylotarg 5 mg",
"name_fr": "Mylotarg 5 mg",
"name_nl": "Mylotarg 5 mg",
"amp_code": "SAM529937-00",
"strengths": [
"5.0000"
],
"pack_count": 1,
"substances": [
"Gemtuzumab Ozogamicin",
"Disodium Hydrogen Phosphate Anhydrous",
"Sodium Chloride",
"Sodium Dihydrogen Phosphate Monohydrate",
"Sucrose"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Gemtuzumab Ozogamicin",
"authorisation_numbers": [
"EU/1/18/1277/001"
]
}See everything about gemtuzumab ozogamicin.
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.