Switzerland· 65225002

Cosentyx

A secukinumab product containing secukinumabum, registered in Switzerland and dispensed under Swissmedic category B, on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

Reimbursed in Switzerland (BAG SL)Cat B (Swissmedic)ATC L04AC10

Checked against BAG Spezialitätenliste (Switzerland) on

Informational only — not a medical device.

SOURCE REGISTER · CHBAG Spezialitätenliste (Switzerland)normalisedCosentyxATCL04AC10REGISTER NO.65225002PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Secukinumab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AC10 (secukinumab), each read from that country’s own register.

  • This record: Switzerland, from BAG Spezialitätenliste (Switzerland)
  • 9 of them publish a price we can compare per daily dose

Secukinumab · ATC L04AC10

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

Price per daily dose

What a daily dose of secukinumab costs, country by country.

Normalised to the WHO defined daily dose (10 mg), so markets compare like for like.

  • Switzerland: $48.03 per daily dose (median across products in the class)
  • Public list prices, converted to USD at the rate date shown

Secukinumab · price per daily dose (10 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$48.03
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

BAG Spezialitätenliste (Switzerland)
Active substance
secukinumabum
Manufacturer
—
Country
Switzerland (CH)
ATC code
L04AC10
ATC class
Secukinumab
Defined daily dose
10 mg, P
Swissmedic category
B
Reimbursed
Yes
Source register
BAG Spezialitätenliste (Switzerland)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • gtin
    7680652250027
    Fertspr 2 Stk
    CHF 1185.1

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

150 interactions on record for secukinumab.

Graded by severity as the source publishes them — 27 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

Secukinumab · interactions on record

150 records

  • 27 severe
  • 116 moderate
  • 7 minor

Most severe, free to view

  • CladribineL01BB04severe
  • Talimogene laherparepvecL01XL02severe
  • Talimogen laherparepvecL01XX51severe
  • LeflunomidL04AA13severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Secukinumab in 15 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All secukinumab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Cosentyx
  • Liechtenstein · Cosentyx
  • Norway · Cosentyx

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/b92b5283-1617-4115-bb8c-025b5f84f617
GET /v1/drugs/b92b5283-1617-4115-bb8c-025b5f84f617?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": "secukinumabum 150 mg",
  "valid_from": "2016-11-01",
  "limitations": "[{\"description\":\"<b>Schwere Plaque-Psoriasis</b><br>\\nBehandlung erwachsener Patienten und Kindern ab 6 Jahren mit schwerer Plaque-Psoriasis, bei denen eine Phototherapie oder eine der folgenden konventionellen systemischen Therapien (Ciclosporin, Methotrexat, Acitretin) keinen therapeutischen Erfolg gezeigt haben. Falls nach 12 Wochen kein therapeutischer Erfolg eingetreten ist, ist die Behandlung abzubrechen. Nach erfolgten Startdosen in den Wochen 0, 1, 2, 3 und 4 wird pro Verabreichung eine maximale Dosis von 300 mg pro Monat vergütet.<br>\\nDie Verschreibung von COSENTYX in der Indikation schwere Plaque-Psoriasis kann nur durch Fachärzte der Dermatologie oder dermatologische Universitätskliniken/Polikliniken erfolgen.<br>\\n<br>\\n\\n\\n\",\"costApproval\":null,\"indication\":\"20311.01\",\"isNew\":false,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2024-05-01\",\"validTo\":null},{\"description\":\"<b>Aktive Psoriasis-Arthritis</b><br>\\nAlleine oder in Kombination mit Methotrexat zur Behandlung erwachsener Patienten mit aktiver Psoriasis Arthritis, die unzureichend auf eine vorhergehende Therapie mit krankheitsmodifizierenden Antirheumatika (disease-modifying anti-rheumatic drugs, DMARD) angesprochen haben. Falls nach 16 Wochen kein therapeutischer Erfolg eingetreten ist, ist die Behandlung abzubrechen.<br> \\nDie Verschreibung von COSENTYX in der Indikation aktive Psoriasis Arthritis kann nur durch Fachärzte der Dermatologie oder Rheumatologie oder dermatologische oder rheumatologische Universitätskliniken/Polikliniken erfolgen.<br>\\n<br>\",\"costApproval\":null,\"indication\":\"20311.02\",\"isNew\":false,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2024-05-01\",\"validTo\":null},{\"description\":\"<b>Aktive ankylosierende Spondylitis / Morbus Bechterew (nur 150 mg)</b><br>\\nZur Behandlung erwachsener Patienten mit schwerer, aktiver ankylosierender Spondylitis (Morbus Bechterew), die unzureichend auf konventionelle Therapie (beispielsweise NSAIDs) angesprochen haben.<br> \\nDie Verschreibung von COSENTYX in der Indikation aktive ankylosierende Spondylitis/Morbus Bechterew kann nur durch Fachärzte der Rheumatologie oder rheumatologische Universitätskliniken/Polikliniken erfolgen.<br>\\n<br>\",\"costApproval\":null,\"indication\":\"20311.03\",\"isNew\":false,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2024-05-01\",\"validTo\":null},{\"description\":\"<b>Juvenile idiopathische Arthritis (JIA) (nur 75 mg und 150 mg)</b><br>\\nBehandlung bei Patienten ab 6 Jahren mit aktiver Enthesitis-assoziierter Arthritis (EAA) oder aktiver juveniler Psoriasis-Arthritis (jPsA), deren Erkrankung nur unzureichend auf nichtsteroidale entzündungshemmende Medikamente (NSAIDs) und krankheitsmodifizierende Antirheumatika (DMARDs) angesprochen hat.<br> Falls nach 12 Wochen kein therapeutischer Erfolg eingetreten ist, muss die Therapie abgebrochen werden.<br> \\nDie Verschreibung von COSENTYX in der Indikation juvenile idiopathische Arthritis kann nur durch Fachärzte der Rheumatologie oder rheumatologische Universitätskliniken/Polikliniken erfolgen.<br>\\n<br>\",\"costApproval\":null,\"indication\":\"20311.04\",\"isNew\":false,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2024-05-01\",\"validTo\":null}]",
  "galenic_form": "Inj Lös 150 mg/1ml",
  "therapeutic_area": null,
  "sl_inclusion_date": "2015-04-01",
  "self_retention_pct": 10
}

See everything about secukinumab.

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.