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.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
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
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_idEU/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.
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.
- BelgiumTavlesse 100 mgInstituto Grifols
- CzechiaTAVLESSEInstituto Grifols, S.A., Barcelona
- SpainTAVLESSE 100 MG COMPRIMIDOS RECUBIERTOS CON PELICULAInstituto Grifols S.A.
- FinlandTavlesseInstituto Grifols S.A.
- FranceTAVLESSE 100 mg, comprimé pelliculéINSTITUTO GRIFOLS
- IrelandTavlesse 100 mg film-coated tabletsRigel Pharmaceuticals B.V.
- IcelandTAVLESSEInstituto Grifols S.A.*
- NorwayTavlesseInstituto Grifols S.A
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.