Switzerland· 68008001
Tysabri 150 mg/ml, Injektionslösung in einer Fertigspritze
A natalizumab product containing natalizumabum, registered in Switzerland by Biogen Switzerland AG and dispensed under Swissmedic category B, on the national reimbursement list. The same ATC class is registered in 11 of our 19 countries.
Checked against Swissmedic (Switzerland) on
Informational only — not a medical device.
Where it is registered
Natalizumab is registered in 11 of 19 countries.
Countries holding a registration under ATC L04AG03 (natalizumab), each read from that country’s own register.
- This record: Switzerland, from Swissmedic (Switzerland)
- 7 of them publish a price we can compare per daily dose
Natalizumab · ATC L04AG03
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
Swissmedic (Switzerland)- Active substance
- natalizumabum
- Manufacturer
- Biogen Switzerland AG
- Country
- Switzerland (CH)
- ATC code
- L04AG03
- ATC class
- Natalizumab
- Defined daily dose
- 10 mg, P
- Swissmedic category
- B
- Reimbursed
- Yes
- Source register
- Swissmedic (Switzerland)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- gtin76806800800162 Fertspr 1 mlCHF 1700.05
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
323 interactions on record for natalizumab.
Graded by severity as the source publishes them — 301 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
Natalizumab · interactions on record
323 records
- 301 severe
- 15 moderate
- 7 minor
Most severe, free to view
- PrednisoloneA07EA01severe
- HydrocortisoneA07EA02severe
- PrednisoneA07EA03severe
- BetamethasoneA07EA04severe
- 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
Natalizumab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandTyrukoAbacus Medicine A/S
- CzechiaTYRUKOSandoz GmbH, Kundl
- BelgiumTyruko 300 mgSandoz
- IrelandTyruko 300 mg concentrate for solution for infusionPolpharma Biologics S.A.
- IcelandTyrukoSandoz GmbH*
- NetherlandsTyruko 300 mg concentraat voor oplossing voor infusieSandoz GmbH
- PolandTyrukoSandoz GmbH
- SwedenTyruko 300 mg Koncentrat till infusionsvätska, lösningSandoz GmbH
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tyruko, Tysabri
- Liechtenstein · Tyruko, Tysabri
- Norway · Tyruko, Tysabri
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 Swissmedic (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/dd2a98af-1385-46b8-83c2-03c7f43b9f57 GET /v1/drugs/dd2a98af-1385-46b8-83c2-03c7f43b9f57?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": "natalizumabum 150 mg",
"valid_from": "2022-01-01",
"limitations": "[{\"description\":\"Bei der Indikationsstellung bzw. vor Therapiebeginn ist das PML-Risiko (PML = progressive multifokale Leukoenzephalopathie) zu berücksichtigen.<br>\\nAls krankheitsmodifizierende Monotherapie von hochaktiver, schubförmig remittierend verlaufender Multipler Sklerose (MS) bei folgenden Patientengruppen:<br>\\n -\\tPatienten mit hoher Krankheitsaktivität trotz Behandlung mit einer krankheitsmodifizierenden Therapie (in der Regel während mindestens 6 Monaten), oder<br>\\n -\\tPatienten mit rasch fortschreitender schubförmig remittierend verlaufender Multipler Sklerose, definiert durch 2 oder mehr Schübe mit Behinderungscharakter in einem Jahr, und mit 1 oder mehr Gadolinium anreichernden Läsionen im MRI des Gehirns oder mit einer signifikanten Erhöhung der T2-Läsionen im Vergleich zu einem kürzlich durchgeführten MRI.<br>\\nAls krankheitsmodifizierende Monotherapie von Patienten mit aktiver, schubförmig remittierend verlaufender MS mit einem negativen anti-JCV Antikörperstatus.<br>\\nDie Behandlung bedarf der Kostengutsprache durch den Krankenversicherer nach vorgängiger Konsultation des Vertrauensarztes.<br>\\nBehandlung durch einen Facharzt der Neurologie mit zeitlichem Zugang zu MRI.<br>\\n<br>\\n\",\"costApproval\":null,\"isNew\":false,\"limitationCode\":null,\"priceModel\":null,\"validFrom\":\"2022-01-01\"}]",
"galenic_form": "Inj Lös 150 mg/ml",
"therapeutic_area": null,
"sl_inclusion_date": "2022-01-01",
"self_retention_pct": 10
}See everything about natalizumab.
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.