Sweden· SE-20151014000068
Repatha 420 mg Injektionsvätska, lösning i cylinderampull
A medicinal product containing evolocumab, registered in Sweden by Amgen Europe B.V..
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
- Evolocumab
- Manufacturer
- Amgen Europe B.V.
- 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_varunummer20151014000068
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Evolocumab in 16 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaREPATHAAmgen Europe B.V., Breda
- BelgiumRepatha 420 mgAmgen Europe
- IcelandRepathaAmgen Europe B.V.*
- PolandRepathaAmgen Europe B.V.
- United StatesREPATHAAmgen USA Inc.
- FinlandRepathaAmgen Europe B.V.
- IrelandRepatha 140 mg solution for injection in pre-filled penAmgen Europe B.V.
- SpainREPATHA 140 MG SOLUCION INYECTABLE EN PLUMA PRECARGADAAmgen Europe B.V.
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Iceland · Repatha
- Norway · Repatha
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/a53d114e-01f9-4f01-a60b-20c8970196de GET /v1/drugs/a53d114e-01f9-4f01-a60b-20c8970196de?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": "20151014000068",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20151014000068",
"product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/repatha-epar-product-information_sv.pdf"
}See everything about evolocumab.
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.