Finland· FI-REL-REL56786
Gavreto
A pralsetinib product containing pralsetinib, registered in Finland by Blueprint Medicines Netherlands B.V.. The same ATC class is registered in 8 of our 19 countries.
Checked against Fimea (Finland) on
Informational only — not a medical device.
Where it is registered
Pralsetinib is registered in 8 of 19 countries.
Countries holding a registration under ATC L01EX23 (pralsetinib), each read from that country’s own register.
- This record: Finland, from Fimea (Finland)
- 6 of them publish a price we can compare per daily dose
Pralsetinib · ATC L01EX23
8 / 19 countries
- Belgiumprice
- Denmark
- Finlandprice
- Franceprice
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
Fimea (Finland)- Active substance
- Pralsetinib
- Manufacturer
- Blueprint Medicines Netherlands B.V.
- Country
- Finland (FI)
- ATC code
- L01EX23
- ATC class
- Pralsetinib
- Defined daily dose
- 0.4 g, O
- 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.
Interactions
93 interactions on record for pralsetinib.
Graded by severity as the source publishes them — 16 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
Pralsetinib · interactions on record
93 records
- 16 severe
- 77 moderate
Most severe, free to view
- KetoconazoleH02CA03severe
- ClarithromycinJ01FA09severe
- KetoconazoleJ02AB02severe
- Darunavir and cobicistatJ05AR14severe
- 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
Pralsetinib in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesGavretoRigel Pharmaceuticals, Inc.
- SpainGAVRETO 100 MG CAPSULAS DURASBlueprint Medicines (Netherlands) B.V.
- FranceGAVRETO 100 mg, géluleBLUEPRINT MEDICINES (PAYS-BAS))
- BelgiumGavreto 100 mgBlueprint Medicines (Netherlands)
- NorwayGavretoRoche
- PolandGavretoRoche Registration GmbH
- United KingdomGavreto 100mg capsulesBlueprint Medicines (UK) Ltd
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/dd76fdeb-4849-4edf-a4da-a75ff3fc0480 GET /v1/drugs/dd76fdeb-4849-4edf-a4da-a75ff3fc0480?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": "0.4",
"form": "kapseli, kova",
"route": "Suun kautta",
"ddd_unit": "g",
"strength": "100 mg",
"atc_label": "pralsetinibi",
"ma_number": null,
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": "EU/1/21/1555/001-003",
"fimea_rel_id": "REL56786",
"authorised_at": "2021-11-18"
}See everything about pralsetinib.
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.