Back to search

Sweden· SE-20110630000258

Fycompa 8 mg Filmdragerad tablett

A medicinal product containing perampanel, registered in Sweden by Eisai GmbH.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedFycompa 8 mg Filmdragerad tablettATC—REGISTER NO.SE-20110630000258PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Perampanel
Manufacturer
Eisai GmbH
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_varunummer
    20110630000258

Regulatory notes

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

Same medicine, other countries

Perampanel in 16 other countries

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

All perampanel products

Authorised across Europe · EMA

The same active substance is authorised in 18 EEA countries. Names it is sold under:

  • Austria · Fypalan, Perampanel Ratiopharm
  • Cyprus · Fylepsia
  • Czechia · Fypalan, Perampanel Orion
  • Germany · Fylepsia, Fypalan
  • Denmark · Perampanel Orion, Perampanel Vivanta
  • Spain · Perampanel Cinfa, Perampanel Combix
  • Finland · Perampanel Orion
  • France · Perampanel Teva
  • United Kingdom (Northern Ireland) · Perampanel Aspire, Perampanel G.L. Pharma
  • Greece · Fylepsia, Perampanel Win Medica
  • Iceland · Fycompa
  • Italy · Fypalan, Perampanel Doc
  • Liechtenstein · Fycompa
  • Netherlands · Fypalan, Perampanel Sandoz
  • Norway · Fycompa, Perampanel Orion
  • Poland · Fypalan, Perampanel Orion
  • Portugal · Perampanel Teva
  • Slovakia · Fypalan

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/9c01ac4d-cede-4dd3-915e-061d57dee1e8
GET /v1/drugs/9c01ac4d-cede-4dd3-915e-061d57dee1e8?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": [
    "EMA",
    "EPAR"
  ],
  "se_npl_id": "20110630000258",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20110630000258",
  "product_doc_link": "https://www.ema.europa.eu/en/medicines/human/EPAR/fycompa"
}

See everything about perampanel.

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.