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Belgium· BE-AMP-SAM660447-00

Nexviadyme 100 mg

A avalglucosidase alfa product containing avalglucosidase alfa, registered in Belgium by Sanofi. The same ATC class is registered in 14 of our 19 countries.

ATC A16AB22

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedNexviadyme 100 mgATCA16AB22REGISTER NO.BE-AMP-SAM660447-00PACKS LISTED4CHECKEDSeptember 26, 2026

Where it is registered

Avalglucosidase alfa is registered in 14 of 19 countries.

Countries holding a registration under ATC A16AB22 (avalglucosidase alfa), each read from that country’s own register.

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

Avalglucosidase alfa · ATC A16AB22

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • 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.

Price per daily dose

What a daily dose of avalglucosidase alfa costs, country by country.

Normalised to the WHO defined daily dose (0.1 g), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Avalglucosidase alfa · price per daily dose (0.1 g)

USD · FX 28 Sept 2026

  • CH Switzerland$1265.54
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Avalglucosidase Alfa
Manufacturer
Sanofi
Country
Belgium (BE)
ATC code
A16AB22
ATC class
Avalglucosidase alfa
Defined daily dose
0.1 g, P
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 4

  • be_apb
    4612669
  • be_apb
    4612644
  • be_apb
    7738131
  • be_apb
    4612651

Regulatory notes

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

Same medicine, other countries

Avalglucosidase alfa in 15 other countries

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

All avalglucosidase alfa products

Authorised across Europe · EMA

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

  • Iceland · Nexviadyme
  • Liechtenstein · Nexviadyme
  • Norway · Nexviadyme

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/c55d0754-c86f-4ec1-a30e-108808961c8e
GET /v1/drugs/c55d0754-c86f-4ec1-a30e-108808961c8e?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": "Nexviadyme 100 mg",
  "name_fr": "Nexviadyme 100 mg",
  "name_nl": "Nexviadyme 100 mg",
  "amp_code": "SAM660447-00",
  "strengths": [
    "100.0000",
    "100.0000"
  ],
  "pack_count": 4,
  "substances": [
    "Avalglucosidase Alfa",
    "Mannitol",
    "Polysorbate 80"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Avalglucosidase Alfa",
  "authorisation_numbers": [
    "EU/1/21/1579/004",
    "EU/1/21/1579/003",
    "EU/1/21/1579/001",
    "EU/1/21/1579/002"
  ]
}

See everything about avalglucosidase alfa.

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.