Germany· DE-A57-f1b8a6bb34a18cfc
Prick-Testlösung Wiesenlieschgras
A medicinal product containing phleum pratense, registered in Germany by Allergopharma Gmbh & Co. Kg.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Phleum Pratense
- Manufacturer
- Allergopharma Gmbh & Co. Kg
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Phleum pratense in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenGrazax 75 000 SQ-T Frystorkad sublingual tablettOrifarm AB
- SpainGRAZAX 75000 SQ-T LIOFILIZADO SUBLINGUALAlk-Abello A/S
- IcelandAlutard SQ (Phleum pratense)ALK-Abelló A/S
- IrelandSoluprick SQ Timothy Grass (Phleum pratense) pollen 10 HEP Solution for skin-prick testingALK-Abello A/S
- NorwayGrazaxALK-Abelló AS
Authorised across Europe · EMA
The same active substance is authorised in 26 EEA countries. Names it is sold under:
- Austria · Grazax
- Belgium · Grazax, Soluprck Sq
- Bulgaria · Гразакс
- Czechia · Grazax, Soluprick Sq
- Denmark · Grazax, Soluprick Sq
- Estonia · Grazax
- Spain · Grazax, Soluprick
- Finland · Grazax, Soluprick Sq
- France · Grazax, Soluprick Sq
- United Kingdom (Northern Ireland) · Grazax, Soluprick Sq
- Croatia · Grazax
- Hungary · Grazax
- Ireland · Grazax, Soluprick Sq
- Iceland · Grazax, Soluprick Sq
- Italy · Grazax
- Lithuania · Grazax
- Luxembourg · Grazax, Soluprck Sq
- Latvia · Grazax
- Netherlands · Grazax, Soluprick Sq
- Norway · Grazax, Soluprick Sq
- Poland · Grazax
- Portugal · Grazax
- Romania · Grazax
- Sweden · Grazax, Soluprick Sq
- Slovenia · Grazax
- Slovakia · Grazax, Soluprick
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 EMA Article 57 (European Union). 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/d5c6e024-eee6-42ff-8b25-13c6da0857d9 GET /v1/drugs/d5c6e024-eee6-42ff-8b25-13c6da0857d9?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.
{
"pzn": null,
"route": "Cutaneous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Phleum Pratense",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about phleum pratense.
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.