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France· FR:66316458

OXLUMO 94,5 mg/0,5mL, solution injectable

A lumasiran product containing lumasiran sodique, registered in France by ALNYLAM NETHERLANDS (PAYS-BAS), on the national reimbursement list. The same ATC class is registered in 12 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC A16AX18

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedOXLUMO 94,5 mg/0,5mL, solution inject…ATCA16AX18REGISTER NO.FR:66316458PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Lumasiran is registered in 12 of 19 countries.

Countries holding a registration under ATC A16AX18 (lumasiran), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 8 of them publish a price we can compare per daily dose

Lumasiran · ATC A16AX18

12 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Netherlands
  • 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

Base de données publique des médicaments — BDPM (France)
Active substance
LUMASIRAN SODIQUE
Manufacturer
ALNYLAM NETHERLANDS (PAYS-BAS)
Country
France (FR)
ATC code
A16AX18
ATC class
Lumasiran
Defined daily dose
2.3 mg, P
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • cip13
    3400930217443
    1 flacon(s) en verre de 0,5 ml
    EUR 46.93

Regulatory notes

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

Same medicine, other countries

Lumasiran in 8 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All lumasiran products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Oxlumo
  • Liechtenstein · Oxlumo
  • Norway · Oxlumo

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 Base de données publique des médicaments — BDPM (France). 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/dc0b2fa1-a731-4f43-960e-7ca03fa7218b
GET /v1/drugs/dc0b2fa1-a731-4f43-960e-7ca03fa7218b?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.

{
  "cis": "66316458",
  "date_amm": "2020-11-19",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/20/1496",
  "substance": "LUMASIRAN SODIQUE",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution injectable",
  "voies_administration": "sous-cutanée",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about lumasiran.

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.