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Sweden· SE-20250402000069

Raxeva 2,5 mg/50 mg Kapsel, hård

A medicinal product containing acetylsalicylic acid + rivaroxaban, registered in Sweden by PharOS - Pharmaceutical Oriented Services Ltd.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedRaxeva 2,5 mg/50 mg Kapsel, hårdATC—REGISTER NO.SE-20250402000069PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Acetylsalicylic Acid + Rivaroxaban
Manufacturer
PharOS - Pharmaceutical Oriented Services 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_varunummer
    20250402000069

Regulatory notes

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

Same medicine, other countries

Acetylsalicylic acid + rivaroxaban in 3 other countries

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

All acetylsalicylic acid + rivaroxaban products

Authorised across Europe · EMA

The same active substance is authorised in 12 EEA countries. Names it is sold under:

  • Austria · Runaplax Ass, Xanirva Duo
  • Czechia · Xanirva Duo
  • Germany · Rivaroxaass Apontis
  • France · Trovunex
  • Croatia · Hypolivat
  • Hungary · Rivaroxaban/Asa Sandoz, Xavipiran
  • Italy · Rivaroxaban E Acido Acetilsalicilico Doc
  • Malta · Raxeva, Rivaroxaban/Acetylsalicylic Acid Pharos
  • Portugal · Xanirva Duo
  • Romania · Xanirva Duo
  • Slovenia · Runaplax Combo
  • Slovakia · Rivaroxaban/Acetylsalicylic Acid Sandoz, Xanirva Duo

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/f711f2ef-2159-40f7-b64f-1a8f04d82253
GET /v1/drugs/f711f2ef-2159-40f7-b64f-1a8f04d82253?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": [
    "SmPC",
    "PL",
    "sPAR",
    "PAR",
    "sRMP"
  ],
  "se_npl_id": "20250402000069",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20250402000069",
  "product_doc_link": "https://docetp.mpa.se/LMF/Raxeva%20capsule%2C%20hard%20ENG%20SmPC_09001bee84e85d8a.pdf"
}

See everything about acetylsalicylic acid + rivaroxaban.

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.