Finland· FI-REL-REL60729

Arexvy

A respiratorisches-synzytial-virus impfstoffe product containing respiratory syncytial virus, glycoprotein f, recombinant, stabilised in the pre-fusion conformation, adjuvanted with as01e, registered in Finland by GlaxoSmithKline Biologicals SA. The same ATC class is registered in 11 of our 19 countries.

ATC J07BX05

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedArexvyATCJ07BX05REGISTER NO.FI-REL-REL60729PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Respiratorisches-synzytial-virus impfstoffe is registered in 11 of 19 countries.

Countries holding a registration under ATC J07BX05 (respiratorisches-synzytial-virus impfstoffe), each read from that country’s own register.

  • This record: Finland, from Fimea (Finland)
  • 7 of them publish a price we can compare per daily dose

Respiratorisches-synzytial-virus impfstoffe · ATC J07BX05

11 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
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

Fimea (Finland)
Active substance
Respiratory syncytial virus, glycoprotein F, recombinant, stabilised in the pre-fusion conformation, adjuvanted with AS01E
Manufacturer
GlaxoSmithKline Biologicals SA
Country
Finland (FI)
ATC code
J07BX05
ATC class
Respiratorisches-Synzytial-Virus Impfstoffe
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.

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/bef5bf98-aa7f-4cdd-883c-61702d46a7b4
GET /v1/drugs/bef5bf98-aa7f-4cdd-883c-61702d46a7b4?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": "injektiokuiva-aine ja suspensio, suspensiota varten",
  "route": "Lihakseen",
  "ddd_unit": null,
  "strength": null,
  "atc_label": "RS-virus-rokotteet",
  "ma_number": null,
  "auth_status": "Myyntilupa myönnetty",
  "eu_ma_number": "EU/1/23/1740/001-002",
  "fimea_rel_id": "REL60729",
  "authorised_at": "2023-06-06"
}

See everything about respiratorisches-synzytial-virus impfstoffe.

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.