Poland· PL-100388509
Everolimus Synthon
A everolimus product containing everolimusum, registered in Poland by Synthon B.V.. The same ATC class is registered in 3 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Everolimus is registered in 3 of 19 countries.
Countries holding a registration under ATC L01XE10 (everolimus), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 2 of them publish a price we can compare per daily dose
Everolimus · ATC L01XE10
3 / 19 countries
- Ireland
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Everolimusum
- Manufacturer
- Synthon B.V.
- Country
- Poland (PL)
- ATC code
- L01XE10
- ATC class
- Everolimus
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 3
- gtin05909991385422
- gtin05909991385439
- gtin05909991385446
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
430 interactions on record for everolimus.
Graded by severity as the source publishes them — 165 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
Everolimus · interactions on record
430 records
- 165 severe
- 255 moderate
- 8 minor
Most severe, free to view
- AprepitantA04AD12severe
- NeomycinA07AA01severe
- StreptomycinA07AA04severe
- Polymyxin BA07AA05severe
2 more interactions with mechanism and management, from a commercially licensed source.
Sign in to check- 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
Everolimus in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaAFINITORNovartis Europharm Limited, Dublin
- NetherlandsAfinitor 10 mg, tablettenNovartis Europharm Limited
- United StatesAfinitorNovartis Pharmaceuticals Corporation
- SpainAFINITOR 10 MG COMPRIMIDOSNovartis Europharm Limited
- SwedenAfinitor 10 mg TablettNovartis Europharm Limited
- FinlandAfinitorOrifarm Oy
- United KingdomAfinitor 10mg tabletsNovartis Pharmaceuticals UK Ltd
- FranceAFINITOR 10 mg, comprimésNOVARTIS EUROPHARM (IRLANDE)
Authorised across Europe · EMA
The same active substance is authorised in 30 EEA countries. Names it is sold under:
- Austria · Certican, Everolimus Ethypharm
- Belgium · Certican, Everolimus Eg
- Bulgaria · Еверолимус Крка, Еверолимус Майлан
- Cyprus · Certican, Everolimus Pharmazac
- Czechia · Certican, Everolimus Accord
- Germany · Certican, Everofin
- Denmark · Certican, Everolimus Krka
- Estonia · Certican, Everolimus Krka
- Spain · Certican, Everolimus Accord
- Finland · Aderolio, Certican
- France · Certican, Everolimus Arrow
- United Kingdom (Northern Ireland) · Aderolio, Aderolio 250 Mcg Tablets
- Greece · Certican, Everolimus Faran
- Croatia · Certican, Everolimus Krka
- Hungary · Certican, Everolimus Accord
- Ireland · Certican, Everolimus Tad
- Iceland · Afinitor, Certican
- Italy · Certican, Everolimus Accord
- Liechtenstein · Afinitor, Votubia
- Lithuania · Certican, Everolimus Norameda
- Luxembourg · Certican, Everolimus Eg
- Latvia · Certican, Everolimus Norameda
- Malta · Certican, Everolimus Ascend
- Netherlands · Certican, Certican Dispers
- Norway · Afinitor, Certican
- Portugal · Certican, Everolimus Ethypharm
- Romania · Certican, Everolimus Accord
- Sweden · Certican, Everolimus Avansor
- Slovenia · Certican, Everolimus Krka
- Slovakia · Certican, Everolimus Accord
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 URPL (Poland). 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/048340dc-7ea2-4d92-89f8-1fd4a4c41eaa GET /v1/drugs/048340dc-7ea2-4d92-89f8-1fd4a4c41eaa?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": "Tabletki",
"source": "urpl",
"strength": "10 mg",
"packaging": "05909991385422 ¦ Rpz ¦ 129919\n10 tabl.\n05909991385439 ¦ Rpz ¦ 129920\n30 tabl.\n05909991385446 ¦ Rpz ¦ 129921\n90 tabl.",
"substance": "Everolimusum 10 mg",
"common_name": "Everolimusum",
"pl_product_id": "100388509",
"pozwolenie_nr": "24967",
"auth_procedure": "DCP",
"authorisation_validity": "Bezterminowe"
}See everything about everolimus.
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.