Ireland· IE-PA-PA1019/007/001
Bricanyl 500 micrograms/ml solution for injection or infusion
A terbutaline product containing terbutaline sulfate, registered in Ireland by AstraZeneca AB. The same ATC class is registered in 4 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Terbutaline is registered in 4 of 19 countries.
Countries holding a registration under ATC R03CC03 (terbutaline), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 3 of them publish a price we can compare per daily dose
Terbutaline · ATC R03CC03
4 / 19 countries
- Czechiaprice
- Finlandprice
- Ireland
- Norwayprice
The record
At a glance
HPRA (Ireland)- Active substance
- Terbutaline sulfate
- Manufacturer
- AstraZeneca AB
- Country
- Ireland (IE)
- ATC code
- R03CC03
- ATC class
- Terbutaline
- Defined daily dose
- 15 mg, O
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA1019/007/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
486 interactions on record for terbutaline.
Graded by severity as the source publishes them — 80 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
Terbutaline · interactions on record
486 records
- 80 severe
- 379 moderate
- 27 minor
Most severe, free to view
- PapaverineA03AD01severe
- CisaprideA03FA02severe
- DolasetronA04AA04severe
- QuinidineC01BA01severe
- 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
Terbutaline in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomBricanyl 1.5mg/5ml syrupAstraZeneca UK Ltd
- United StatesTerbutaline SulfateANI Pharmaceuticals, Inc.
- FinlandBricanylAstraZeneca Oy
- NorwayBricanylAstraZeneca
- SwedenBricanyl 0,5 mg/ml Injektionsvätska/koncentrat till infusionsvätska, lösningAstraZeneca AB
- FranceBRICANYL 0,5 mg/1 ml, solution injectable en ampouleASTRAZENECA
- GermanyAerodur TurbohalerAstrazeneca Gmbh
- IcelandBricanyl TurbuhalerAstraZeneca A/S
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Bricanyl
- Cyprus · Ataline
- Czechia · Bricanyl
- Germany · Aerodur Turbohaler, Bricanyl
- Denmark · Bricanyl Turbuhaler
- Spain · Terbasmin, Terbasmin Turbuhaler
- Finland · Bricanyl Turbuhaler
- France · Bricanyl, Bricanyl Turbuhaler
- United Kingdom (Northern Ireland) · Bricanyl, Bricanyl Respules
- Hungary · Bricanyl
- Iceland · Bricanyl Turbuhaler
- Malta · Bricanyl Turbohaler
- Netherlands · Bricanyl Turbuhaler
- Norway · Bricanyl, Bricanyl Turbuhaler
- Portugal · Bricanyl Turbohaler
- Sweden · Bricanyl, Bricanyl Turbuhaler
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/f5be0853-83b6-4069-b550-8eec18a2763e GET /v1/drugs/f5be0853-83b6-4069-b550-8eec18a2763e?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/infusion",
"routes": [
"Intramuscular use",
"Intravenous use",
"Subcutaneous use"
],
"source": "hpra",
"atc_all": [
"R03CC",
"R03CC03"
],
"strength": null,
"pa_number": "PA1019/007/001",
"substances": [
"Terbutaline sulfate"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Not marketed",
"authorised_at": "01/04/1999",
"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 terbutaline.
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.