Belgium· BE-AMP-SAM529786-00
Lojuxta 30 mg
A lomitapide product containing lomitapide mesylate, registered in Belgium by Chiesi Farmaceutici. The same ATC class is registered in 14 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Lomitapide is registered in 14 of 19 countries.
Countries holding a registration under ATC C10AX12 (lomitapide), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 9 of them publish a price we can compare per daily dose
Lomitapide · ATC C10AX12
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Lomitapide Mesylate
- Manufacturer
- Chiesi Farmaceutici
- Country
- Belgium (BE)
- ATC code
- C10AX12
- ATC class
- Lomitapide
- Defined daily dose
- 40 mg, O
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 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.
Interactions
299 interactions on record for lomitapide.
Graded by severity as the source publishes them — 206 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
Lomitapide · interactions on record
299 records
- 206 severe
- 86 moderate
- 7 minor
Most severe, free to view
- ClotrimazoleA01AB18severe
- AprepitantA04AD12severe
- Chenodeoxycholic acidA05AA01severe
- SulfasalazineA07EC01severe
- 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
Lomitapide in 14 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesJuxtapidPharma Packaging Solutions, LLC dba Tjoapack LLC
- IrelandLojuxta 30 mg hard capsulesChiesi Farmaceutici S.p.A.
- IcelandLojuxtaChiesi Farmaceutici S.p.A.*
- FinlandLojuxtaChiesi Farmaceutici S.p.A.
- PolandLojuxtaChiesi Farmaceutici S.p.A.
- SwedenLojuxta 30 mg Kapsel, hårdChiesi Farmaceutici S.p.A.
- NetherlandsLojuxta 30 mg harde capsulesChiesi Farmaceutici S.p.A.
- SpainLOJUXTA 10 MG CAPSULAS DURASChiesi Farmaceutici S.P.A.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Lojuxta
- Liechtenstein · Lojuxta
- Norway · Lojuxta
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/d2b238bb-7ec0-495b-97c2-0b0c8899200f GET /v1/drugs/d2b238bb-7ec0-495b-97c2-0b0c8899200f?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": "Capsule, hard",
"source": "afmps",
"status": "REVOKED",
"name_en": "Lojuxta 30 mg",
"name_fr": "Lojuxta 30 mg",
"name_nl": "Lojuxta 30 mg",
"amp_code": "SAM529786-00",
"strengths": [
"30.0000",
"30.0000",
"30.0000",
"194.8400"
],
"pack_count": 1,
"substances": [
"Lomitapide Mesylate",
"Lomitapide",
"Lactose",
"Propylene Glycol",
"Sodium Starch Glycolate (Type A)"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Lomitapide",
"authorisation_numbers": [
"EU/1/13/851/004"
]
}See everything about lomitapide.
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.