Finland· FI-REL-REL3367
Samarium (153 Sm)-Edtmp
A samarium (153sm) lexidronam product containing samarium(153sm) + ethylenediaminetetrametylen phosphonate (edtmp), registered in Finland by MAP Medical Technologies Oy. The same ATC class is registered in 8 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Samarium (153sm) lexidronam is registered in 8 of 19 countries.
Countries holding a registration under ATC V10BX02 (samarium (153sm) lexidronam), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 5 of them publish a price we can compare per daily dose
Samarium (153sm) lexidronam · ATC V10BX02
8 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
The record
At a glance
Fimea (Finland)- Active substance
- Samarium(153Sm) + Ethylenediaminetetrametylen phosphonate (EDTMP)
- Manufacturer
- MAP Medical Technologies Oy
- Country
- Finland (FI)
- ATC code
- V10BX02
- ATC class
- Samarium (153Sm) lexidronam
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 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.
Same class
Other records under V10BX02
Samarium (153sm) lexidronam, as other registers publish it.
- DenmarkQuadrametCis Bio International
- PolandQuadrametCIS bio international
- FinlandQuadrametCIS bio international
- IcelandQuadrametCis bio international*
- CzechiaQUADRAMETCIS bio international, Gif-sur-Yvette Cedex
- BelgiumQuadramet 1.3 GBq/mlCis Bio International
- IrelandQuadramet 1.3 GBq/mL solution for injection.CIS bio International
- NetherlandsQUADRAMET, oplossing voor injectie 1,3 GBq/mlCis Bio International
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Fimea (Finland). 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/c3f7583b-b424-495d-a7f3-014862df6091 GET /v1/drugs/c3f7583b-b424-495d-a7f3-014862df6091?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.
{
"ddd": null,
"form": "injektioneste",
"route": null,
"ddd_unit": null,
"strength": "60 - 450 MBq/ml",
"atc_label": "samarium(153Sm)leksidronaami",
"ma_number": "11300",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL3367",
"authorised_at": "1993-11-29"
}See everything about samarium (153sm) lexidronam.
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.