Switzerland· 63025001
Lemtrada
A alemtuzumab product containing alemtuzumabum, registered in Switzerland and dispensed under Swissmedic category A, on the national reimbursement list. The same ATC class is registered in 11 of our 19 countries.
Checked against BAG Spezialitätenliste (Switzerland) on
Informational only — not a medical device.
Where it is registered
Alemtuzumab is registered in 11 of 19 countries.
Countries holding a registration under ATC L04AG06 (alemtuzumab), each read from that country’s own register.
- This record: Switzerland, from BAG Spezialitätenliste (Switzerland)
- 7 of them publish a price we can compare per daily dose
Alemtuzumab · ATC L04AG06
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
BAG Spezialitätenliste (Switzerland)- Active substance
- alemtuzumabum
- Manufacturer
- —
- Country
- Switzerland (CH)
- ATC code
- L04AG06
- ATC class
- Alemtuzumab
- Defined daily dose
- 0.13 mg, P
- Swissmedic category
- A
- Reimbursed
- Yes
- Source register
- BAG Spezialitätenliste (Switzerland)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- gtin7680630250018DurchstfCHF 7223.6
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
338 interactions on record for alemtuzumab.
Graded by severity as the source publishes them — 24 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
Alemtuzumab · interactions on record
338 records
- 24 severe
- 314 moderate
Most severe, free to view
- CladribineL01BB04severe
- PrednisoloneA07EA01moderate
- HydrocortisoneA07EA02moderate
- PrednisoneA07EA03moderate
- 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
Alemtuzumab in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandLemtradaSanofi Belgium
- United KingdomLemtrada 12mg/1.2ml concentrate for solution for infusion vialsSanofi
- CzechiaCAMPATH
- CanadaLEMTRADASANOFI-AVENTIS CANADA INC
- United StatesCampathGenzyme Corporation
- NetherlandsLEMTRADA 12 mg concentraat voor oplossing voor infusieSanofi Belgium
- PolandLemtradaSanofi Belgium
- SwedenLemtrada 12 mg Koncentrat till infusionsvätska, lösningSanofi Belgium
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Lemtrada
- Liechtenstein · Lemtrada
- Norway · Lemtrada
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 BAG Spezialitätenliste (Switzerland). 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/345acebb-3c38-4215-8780-b206eec1da36 GET /v1/drugs/345acebb-3c38-4215-8780-b206eec1da36?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.
{
"unit": null,
"strength": "alemtuzumabum 12 mg",
"valid_from": "2025-01-01",
"limitations": "[{\"description\":\"Bei erwachsenen Patienten mit hochaktiver schubförmig-remittierender Multipler Sklerose (RRMS), wenn zuvor eine vollständige und adäquate Behandlung mit mindestens zwei anderen krankheitsmodifizierenden Therapien (disease modifying treatments - DMTs) durchgeführt wurde oder bei Patienten mit hochaktiver RRMS, bei denen alle anderen DMTs kontraindiziert sind oder aus anderen Gründen nicht geeignet sind.<br>\\nLEMTRADA kann aufgrund des Sicherheitsprofils nur von erfahrenen Fachärzten der Neurologie FMH als Reservemittel in den neurologischen Kliniken der Weiterbildungskategorie A und B (mit Zugang zu Intensivmedizin) eingesetzt werden.<br>\\nEs können maximal 4 Behandlungszyklen LEMTRADA vergütet werden.<br>\\nDie Behandlung bedarf der Kostengutsprache durch den Krankenversicherer nach vorgängiger Konsultation des Vertrauensarztes.<br>\\n<br>\\n\",\"costApproval\":null,\"indication\":\"\",\"isNew\":false,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2025-01-01\",\"validTo\":\"2027-12-31\"}]",
"galenic_form": "Inf Konz 12 mg/1.2ml",
"therapeutic_area": null,
"sl_inclusion_date": "2015-05-01",
"self_retention_pct": 10
}See everything about alemtuzumab.
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.