Ireland· IE-PA-EU/1/18/1340/007-009
TAKHZYRO 150 mg solution for injection in pre-filled syringe
A lanadelumab product containing lanadelumab, registered in Ireland by Takeda Pharmaceuticals International AG Ireland Branch. The same ATC class is registered in 15 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Lanadelumab is registered in 15 of 19 countries.
Countries holding a registration under ATC B06AC05 (lanadelumab), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 10 of them publish a price we can compare per daily dose
Lanadelumab · ATC B06AC05
15 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of lanadelumab costs, country by country.
Normalised to the WHO defined daily dose (21.4 mg), so markets compare like for like.
- 1 market with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Lanadelumab · price per daily dose (21.4 mg)
USD · FX 28 Sept 2026
- CH Switzerland$857.11
The record
At a glance
HPRA (Ireland)- Active substance
- LANADELUMAB
- Manufacturer
- Takeda Pharmaceuticals International AG Ireland Branch
- Country
- Ireland (IE)
- ATC code
- B06AC05
- ATC class
- Lanadelumab
- Defined daily dose
- 21.4 mg, P
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/18/1340/007-009
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lanadelumab in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceTAKHZYRO 150 mg, solution injectable en seringue préremplieTAKEDA PHARMACEUTICALS INTERNATIONAL (IRLANDE)
- NetherlandsTAKHZYRO 150 mg oplossing voor injectie in voorgevulde spuitTakeda Pharmaceuticals International AG Ireland Branch
- CzechiaTAKHZYROTakeda Pharmaceuticals International AG Ireland Branch, Dublin
- United StatesTAKHZYROTakeda Pharmaceuticals America, Inc.
- FinlandTakhzyroOrifarm Oy
- BelgiumTakhzyro 150 mgTakeda Pharmaceuticals International Ireland Branch
- United KingdomTakhzyro 150mg/1ml solution for injection pre-filled syringesTakeda UK Ltd
- IcelandTakhzyroTakeda Pharmaceuticals International AG Ireland Branch
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Takhzyro
- Liechtenstein · Takhzyro
- Norway · Takhzyro
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/7c7bd439-734e-4d18-bd9d-c6a13e31504c GET /v1/drugs/7c7bd439-734e-4d18-bd9d-c6a13e31504c?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": [
"Subcutaneous use"
],
"source": "hpra",
"atc_all": [
"B06AC05"
],
"strength": null,
"pa_number": "EU/1/18/1340/007-009",
"substances": [
"LANADELUMAB"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "15/11/2023",
"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 lanadelumab.
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.