Poland· PL-100108639
Fasturtec
A rasburicase product containing rasburicasum, registered in Poland by Sanofi Winthrop Industrie. The same ATC class is registered in 13 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Rasburicase is registered in 13 of 19 countries.
Countries holding a registration under ATC V03AF07 (rasburicase), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 8 of them publish a price we can compare per daily dose
Rasburicase · ATC V03AF07
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
URPL (Poland)- Active substance
- Rasburicasum
- Manufacturer
- Sanofi Winthrop Industrie
- Country
- Poland (PL)
- ATC code
- V03AF07
- ATC class
- Rasburicase
- Defined daily dose
- 14 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909990943111
- gtin05909990943128
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
25 interactions on record for rasburicase.
Graded by severity as the source publishes them — 1 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
Rasburicase · interactions on record
25 records
- 1 severe
- 24 moderate
Most severe, free to view
- PrilocaineN01BB04severe
- LidocainA01AE01moderate
- TetracainA01AE02moderate
- LidocaineC05AD01moderate
- 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
Rasburicase in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandFasturtec 1.5 mg / 1 ml, poudre et solvant pour solution à diluer pour perfusionSanofi-Aventis (Suisse) SA
- FinlandFasturtecSanofi Winthrop Industrie
- SpainFASTURTEC 1,5 MG/ML POLVO Y DISOLVENTE PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONSanofi Winthrop Industrie
- BelgiumFasturtec 1.5 mg/mlSanofi Winthrop Industrie
- SwedenFasturtec 1,5 mg/ml Pulver och vätska till koncentrat till infusionsvätska, lösningSanofi Winthrop Industrie
- IrelandFasturtec 1.5 mg/ml powder and solvent for concentrate for solution for infusionSanofi Winthrop Industrie
- IcelandFasturtecSanofi Winthrop Industrie
- NorwayFasturtecSanofi Winthrop Industrie
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Fasturtec
- Liechtenstein · Fasturtec
- Norway · Fasturtec
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/b8da4184-9927-4c60-a274-0fb24671d3bd GET /v1/drugs/b8da4184-9927-4c60-a274-0fb24671d3bd?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": "Proszek i rozpuszczalnik do sporządzania koncentratu roztworu do infuzji",
"source": "urpl",
"strength": "1,5 mg/ml",
"packaging": "05909990943111 ¦ Rpz ¦ EU/1/00/170/001 ¦ 19376\n3 fiol. 1,5 mg ¦ 3 amp.-strzyk. 2 ml\n¦ UR/Z/4c/030/23 - 05909990943111\n05909990943128 ¦ Rpz ¦ EU/1/00/170/002 ¦ 20211\n1 fiol. 7,5 mg ¦ 1 amp.-strzyk. 5 ml",
"substance": "Rasburicasum 1.5 mg/ml",
"common_name": "Rasburicasum",
"pl_product_id": "100108639",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about rasburicase.
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.