Ireland· IE-PA-PA0540/139/001
Adenocor 3 mg/ml solution for injection
A adenosine product containing adenosine, registered in Ireland by Sanofi-Aventis Ireland Limited T/A SANOFI. The same ATC class is registered in 16 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Adenosine is registered in 16 of 19 countries.
Countries holding a registration under ATC C01EB10 (adenosine), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 8 of them publish a price we can compare per daily dose
Adenosine · ATC C01EB10
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
HPRA (Ireland)- Active substance
- Adenosine
- Manufacturer
- Sanofi-Aventis Ireland Limited T/A SANOFI
- Country
- Ireland (IE)
- ATC code
- C01EB10
- ATC class
- Adenosine
- Defined daily dose
- 15 mg, P
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA0540/139/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
181 interactions on record for adenosine.
Graded by severity as the source publishes them — 38 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
Adenosine · interactions on record
181 records
- 38 severe
- 90 moderate
- 1 minor
- 52 info
Most severe, free to view
- PapaverineA03AD01severe
- CisaprideA03FA02severe
- DolasetronA04AA04severe
- PapaverinC04AX38severe
- 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
Adenosine in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesAdenosineMylan Institutional LLC
- SpainADENOSCAN 30 mg/10 ml SOLUCION PARA PERFUSIONSanofi Aventis S.A.
- FinlandAdenocorParanova Oy
- United KingdomAdenocor 6mg/2ml solution for injection vialsSanofi
- PolandAdenocorDelfarma Sp. z o.o.
- GermanyAdenoscanSanofi-Aventis Deutschland Gmbh
- FranceADENOSCAN 30 mg/10 mL, solution pour perfusionSANOFI WINTHROP INDUSTRIE
- BelgiumAdenocor 6 mg/2 mlSanofi Belgium
Authorised across Europe · EMA
The same active substance is authorised in 22 EEA countries. Names it is sold under:
- Austria · Adenosin Baxter, Adenosin Hikma
- Belgium · Adenocor, Adenosine Fresenius Kabi
- Cyprus · Caden
- Czechia · Adenocor
- Germany · Adenoscan, Adenosin Altamedics
- Denmark · Adenocor, Adenosin Fresenius Kabi
- Estonia · Adenosin Life Medical
- Spain · Adenocor, Adenoscan
- Finland · Adenosin Life Medical, Adenosin Macure
- France · Adenoscan, Adenosine Hikma
- United Kingdom (Northern Ireland) · Adenocor, Adenoscan
- Greece · Adenorythm
- Hungary · Adenocor
- Italy · Adenoscan, Adenosina Hikma
- Lithuania · Adenosine Life Medical
- Luxembourg · Adenocor
- Netherlands · Adenocor, Adenosine Fresenius Kabi
- Norway · Adenosin Life Medical, Adenosin Macure
- Poland · Adenocor
- Portugal · Adenoscan, Adenosina Baxter
- Sweden · Adenosin Life Medical, Adenosin Macure
- Slovakia · Adenocor
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 HPRA (Ireland). 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/20009bca-a3fa-4364-8a95-f5ddd2d47278 GET /v1/drugs/20009bca-a3fa-4364-8a95-f5ddd2d47278?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": "Solution for injection",
"routes": [
"Intravenous use"
],
"source": "hpra",
"atc_all": [
"C01EB",
"C01EB10"
],
"strength": null,
"pa_number": "PA0540/139/001",
"substances": [
"Adenosine"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "16/06/1994",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about adenosine.
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.