Sweden· SE-20200210000027
Pedmarqsi 80 mg/ml Infusionsvätska, lösning
A medicinal product containing sodium thiosulfate, registered in Sweden by Norgine BV.
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
- Sodium Thiosulfate
- Manufacturer
- Norgine BV
- 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_varunummer20200210000027
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium thiosulfate in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumPedmarqsi 80 mg/mlNorgine
- SwitzerlandPedmarqsi 80 mg/ml, InfusionslösungNorgine AG
- CzechiaPEDMARQSINorgine B.V., Amsterdam
- FinlandPedmarqsiNorgine B.V.
- IrelandPedmarqsi 80 mg/mL solution for infusionNorgine B.V.
- IcelandPedmarqsiNorgine B.V.
- NorwayPedmarqsiNorgine B.V.
- PolandPedmarqsiNorgine B.V.
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Belgium · Thiosulfate De Sodium Sterop
- Germany · Natriumthiosulfat
- France · Oligosol
- United Kingdom (Northern Ireland) · Pedmarqsi, Sodium Thiosulfate Hope Pharmaceuticals
- Ireland · Sodium Thiosulfate Hope Pharmaceuticals
- Iceland · Pedmarqsi
- Italy · Sodio Tiosolfato Monico, Sodio Tiosolfato S.A.L.F.
- Liechtenstein · Pedmarqsi
- Luxembourg · Oligosol
- Netherlands · Natriumthiosulfaat Hope
- Norway · Pedmarqsi
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/68bd0160-e50e-4833-a68a-9df2d09c9990 GET /v1/drugs/68bd0160-e50e-4833-a68a-9df2d09c9990?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": [
"Dispensbeslut",
"EPAR",
"EMA"
],
"se_npl_id": "20200210000027",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20200210000027",
"product_doc_link": "https://docetp.mpa.se/LMF/Pedmarqsi%2C%20injektionsflaska%2C%20100%20ml%2C%20sammanfattning%20av%20beslut%2C%20giltigt%20fr.o.m.%202026-03-27%20t.o.m.%202028-03-27%20%28franska%20f%C3%B6rpackningar%29_09001bee84fe88b3.pdf"
}See everything about sodium thiosulfate.
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.