Sweden· SE-20240502000120
Alyftrek 50 mg/20 mg/4 mg Filmdragerad tablett
A medicinal product containing tezacaftor + deutivacaftor + vanzacaftor, registered in Sweden by Vertex Pharmaceuticals Ireland Ltd.
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Tezacaftor + Deutivacaftor + Vanzacaftor
- Manufacturer
- Vertex Pharmaceuticals Ireland Ltd
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20240502000120
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tezacaftor + deutivacaftor + vanzacaftor in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesALYFTREKVertex Pharmaceuticals Incorporated
- CzechiaALYFTREKVertex Pharmaceuticals (Ireland) Limited, Dublin
- FinlandAlyftrekVertex Pharmaceuticals (Ireland) Limited
- United KingdomAlyftrek 125mg/50mg/10mg tabletsVertex Pharmaceuticals (Europe) Ltd
- IrelandAlyftrek 125 mg/50 mg/10 mg film-coated tabletsVertex Pharmaceuticals (Ireland) Limited
- SwitzerlandAlyftrek
- NetherlandsAlyftrek 125 mg/50 mg/10 mg filmomhulde tablettenVertex Pharmaceuticals (Ireland) Limited
- NorwayAlyftrekVertex Pharmaceuticals (Ireland) Limited
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Alyftrek
- Liechtenstein · Alyftrek
- Norway · Alyftrek
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 Swedish Medical Products Agency (Sweden). 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/e38411f6-ce7c-49eb-8ce4-735ef958dbf8 GET /v1/drugs/e38411f6-ce7c-49eb-8ce4-735ef958dbf8?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.
{
"source": "lakemedelsverket",
"doc_types": [
"EPAR",
"EMA"
],
"se_npl_id": "20240502000120",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20240502000120",
"product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/alyftrek-epar-product-information_sv.pdf"
}See everything about tezacaftor + deutivacaftor + vanzacaftor.
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.