Back to search

Netherlands· NL-b797cea50ec2

Tavlesse 100 mg filmomhulde tabletten

A fostamatinib product containing fostamatinib dinatrium 6-water, registered in Netherlands by Instituto Grifols S.A.. The same ATC class is registered in 13 of our 19 countries.

ATC B02BX09

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedTavlesse 100 mg filmomhulde tablettenATCB02BX09REGISTER NO.NL-b797cea50ec2PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Fostamatinib is registered in 13 of 19 countries.

Countries holding a registration under ATC B02BX09 (fostamatinib), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 7 of them publish a price we can compare per daily dose

Fostamatinib · ATC B02BX09

13 / 19 countries

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

CBG-MEB (Netherlands)
Active substance
FOSTAMATINIB DINATRIUM 6-WATER
Manufacturer
Instituto Grifols S.A.
Country
Netherlands (NL)
ATC code
B02BX09
ATC class
Fostamatinib
Defined daily dose
0.2 g, O
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/19/1405

Regulatory notes

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

Interactions

545 interactions on record for fostamatinib.

Graded by severity as the source publishes them — 50 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

Fostamatinib · interactions on record

545 records

  • 50 severe
  • 493 moderate
  • 2 minor

Most severe, free to view

  • LonafarnibA16AX20severe
  • BerotralstatB06AC06severe
  • ConivaptanC03XA02severe
  • MipomersenC10AX11severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Fostamatinib in 13 other countries

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

All fostamatinib products

Authorised across Europe · EMA

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

  • Iceland · Tavlesse
  • Liechtenstein · Tavlesse
  • Norway · Tavlesse

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 CBG-MEB (Netherlands). 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/a4e7d77d-03b3-4ba3-b9ea-239b1d53114c
GET /v1/drugs/a4e7d77d-03b3-4ba3-b9ea-239b1d53114c?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": "Filmomhulde tablet",
  "route": "Oraal gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/tavlesse-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Fostamatinib",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp123819",
  "excipients": [
    "IJZEROXIDE GEEL (E 172)",
    "IJZEROXIDE ROOD  (E 172)",
    "MACROGOL 3350",
    "MAGNESIUMSTEARAAT (E 470b)",
    "MANNITOL (D-) (E 421)",
    "NATRIUMWATERSTOFCARBONAAT (E 500 (II))",
    "NATRIUMZETMEELGLYCOLAAT",
    "POLYVINYLALCOHOL (E 1203)",
    "POVIDON K 30 (E 1201)",
    "TALK (E 553b)",
    "TITAANDIOXIDE (E 171)"
  ],
  "substances": [
    "FOSTAMATINIB DINATRIUM 6-WATER"
  ],
  "leaflet_url": null,
  "authorised_at": "2020/01/09",
  "procedure_number": "EMEA/H/C/005012",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/19/1405",
  "additional_monitoring": "N"
}

See everything about fostamatinib.

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.