Belgium· BE-AMP-SAM662020-00
Takhzyro 150 mg
A lanadelumab product containing lanadelumab, registered in Belgium by Takeda Pharmaceuticals International Ireland Branch. The same ATC class is registered in 15 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) 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: Belgium, from FAMHP / AFMPS (Belgium)
- 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
FAMHP / AFMPS (Belgium)- Active substance
- Lanadelumab
- Manufacturer
- Takeda Pharmaceuticals International Ireland Branch
- Country
- Belgium (BE)
- ATC code
- B06AC05
- ATC class
- Lanadelumab
- Defined daily dose
- 21.4 mg, P
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 1
- be_apb4857017
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.
- United KingdomTakhzyro 150mg/1ml solution for injection pre-filled syringesTakeda UK Ltd
- CzechiaTAKHZYROTakeda Pharmaceuticals International AG Ireland Branch, Dublin
- IcelandTakhzyroTakeda Pharmaceuticals International AG Ireland Branch
- NorwayTakhzyroTakeda Pharmaceuticals International AG Ireland Branch
- PolandTakhzyroTakeda Pharmaceuticals International AG
- SwitzerlandTAKHZYRO 150 mg, Injektionslösung in einer FertigspritzeTakeda Pharma AG
- SwedenTAKHZYRO 150 mg Injektionsvätska, lösning i förfylld sprutaTakeda Pharmaceuticals International AG Ireland Branch
- SpainTAKHZYRO 150 MG SOLUCION INYECTABLE EN JERINGA PRECARGADATakeda 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 FAMHP / AFMPS (Belgium). 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/84a641e0-bc9e-44bb-be96-99c3ac9dd24c GET /v1/drugs/84a641e0-bc9e-44bb-be96-99c3ac9dd24c?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 in pre-filled syringe",
"source": "afmps",
"status": "AUTHORIZED",
"name_en": "Takhzyro 150 mg",
"name_fr": "Takhzyro 150 mg",
"name_nl": "Takhzyro 150 mg",
"amp_code": "SAM662020-00",
"strengths": [
"150.0000",
"150.0000"
],
"pack_count": 3,
"substances": [
"Lanadelumab",
"Disodium Hydrogen Phosphate Dihydrate",
"Sodium Chloride",
"Polysorbate 80"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Lanadelumab",
"authorisation_numbers": [
"EU/1/18/1340/009",
"EU/1/18/1340/007",
"EU/1/18/1340/008"
]
}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.