Ireland· IE-PA-PA1824/009/001
Pred Mild Sterile Ophthalmic Suspension, 0.12% w/v, Eye Drops, Suspension
A prednisolone product containing prednisolone acetate, registered in Ireland by AbbVie Limited. The same ATC class is registered in 11 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Prednisolone is registered in 11 of 19 countries.
Countries holding a registration under ATC S01BA04 (prednisolone), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 7 of them publish a price we can compare per daily dose
Prednisolone · ATC S01BA04
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Prednisolone acetate
- Manufacturer
- AbbVie Limited
- Country
- Ireland (IE)
- ATC code
- S01BA04
- ATC class
- Prednisolone
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA1824/009/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
41 interactions on record for prednisolone.
Graded by severity as the source publishes them — 41 moderate. 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
Prednisolone · interactions on record
41 records
- 41 moderate
Most severe, free to view
- MiconazoleA07AC01moderate
- LonafarnibA16AX20moderate
- VoxelotorB06AX03moderate
- ConivaptanC03XA02moderate
- 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
Prednisolone in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomDeltacortril 2.5mg gastro-resistant tabletsPhoenix Labs Ltd
- FinlandDeltacortril VetPfizer Oy, Animal Health
- United StatesPRED FORTEAllergan, Inc.
- GermanyDontisolon D MundheilpasteSeptodont Gmbh
- NorwayDi-Adreson-F aquosumACE Pharmaceuticals
- NetherlandsDi-Adreson-F Aquosum 25 mg, poeder voor injectievloeistofACE Pharmaceuticals B.V.
- SwedenPrednisolon Actavis 10 mg TablettActavis Group PTC ehf.
- SwitzerlandPred Forte 1%, AugentropfensuspensionAbbVie AG
Authorised across Europe · EMA
The same active substance is authorised in 29 EEA countries. Names it is sold under:
- Austria · Aprednislon, Prednifluid
- Belgium · Pred Forte
- Bulgaria · Ultracortenol Eye Ointment, Кортапред
- Cyprus · Corotrope, Medopred
- Czechia · Predni-Pos, Ultracortenol
- Germany · Dontisolon D Mundheilpaste, Dontisolon D Zylinderampullen
- Denmark · Prednisolon "omet Pharma", Prednisolon Actavis
- Estonia · Prednisolon Richter, Ultracortenol
- Spain · Estilsona, Paidocort
- Finland · Pred Forte, Prednisolon .
- France · Hydrocortancyl, Prednisolone Activase
- United Kingdom (Northern Ireland) · Deltacortril, Dilacort
- Greece · Adelcort®, Cordivate
- Croatia · Ultracortenol
- Hungary · Prednisolon Richter
- Iceland · Prednisolon Actavis, Prednisolon Eql Pharma
- Italy · Sintredius
- Lithuania · Prednisolon Richter, Ultarcorlene
- Luxembourg · Pred Forte
- Latvia · Prednisolon Richter, Ultarcorlene
- Malta · Corotrope, Pirver
- Netherlands · Di-Adreson-F Aquosum, Pred Forte
- Norway · Prednisolon Actavis, Prednisolon Orifarm Healthcare
- Poland · Encortolon, Pred-Ophtalene
- Portugal · Frisolona Forte, Lepicortinolo
- Romania · Ultracortenol
- Sweden · Prednisolon Actavis, Prednisolon Alternova
- Slovenia · Ultracortenol
- Slovakia · Ultracortenol
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/7fd18c27-5998-49c3-a9b0-581709b1ab46 GET /v1/drugs/7fd18c27-5998-49c3-a9b0-581709b1ab46?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": "Eye drops, suspension",
"routes": [
"Ocular use"
],
"source": "hpra",
"atc_all": [
"S01BA",
"S01BA04"
],
"strength": null,
"pa_number": "PA1824/009/001",
"substances": [
"Prednisolone acetate"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Not marketed",
"authorised_at": "01/04/1977",
"dispensing_status": "Product subject to prescription which may be renewed (B)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about prednisolone.
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.