France· FR:60789511
TEGSEDI 284 mg, solution injectable en seringue préremplie
A inotersen product containing inotersen sodique, registered in France by AKCEA THERAPEUTICS IRELAND (IRLANDE), on the national reimbursement list. The same ATC class is registered in 9 of our 19 countries.
Checked against Base de données publique des médicaments — BDPM (France) on
Informational only — not a medical device.
Where it is registered
Inotersen is registered in 9 of 19 countries.
Countries holding a registration under ATC N07XX15 (inotersen), each read from that country’s own register.
- This record: France, from Base de données publique des médicaments — BDPM (France)
- 6 of them publish a price we can compare per daily dose
Inotersen · ATC N07XX15
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Netherlands
- Polandprice
- United Kingdom
The record
At a glance
Base de données publique des médicaments — BDPM (France)- Active substance
- INOTERSEN SODIQUE
- Manufacturer
- AKCEA THERAPEUTICS IRELAND (IRLANDE)
- Country
- France (FR)
- ATC code
- N07XX15
- ATC class
- Inotersen
- Defined daily dose
- 41 mg, P
- Reimbursed
- Yes
- Source register
- Base de données publique des médicaments — BDPM (France)
- Last checked
- September 12, 2026
Packs & prices · 1
1 priced- cip1334009301548474 seringues préremplies en verre de 1,5 mLEUR 19.53
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
169 interactions on record for inotersen.
Graded by severity as the source publishes them — 143 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Inotersen · interactions on record
169 records
- 143 severe
- 26 moderate
Most severe, free to view
- HeparinB01AB01severe
- NeomycinA07AA01severe
- StreptomycinA07AA04severe
- Polymyxin BA07AA05severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Inotersen in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- IrelandTegsedi 284 mg solution for injection in pre-filled syringeAkcea Therapeutics Ireland Ltd
- SpainTEGSEDI 284 MG SOLUCION INYECTABLE EN JERINGA PRECARGADAAkcea Therapeutics Ireland Limited
- FinlandTegsediAkcea Therapeutics Ireland Ltd
- United KingdomTegsedi 284mg/1.5ml solution for injection pre-filled syringesSwedish Orphan Biovitrum Ltd
- IcelandTegsediAkcea Therapeutics Ireland Ltd
- NetherlandsTegsedi 189 mg/ml, oplossing voor injectie in voorgevulde spuitAkcea Therapeutics Ireland Ltd
- PolandTegsediAkcea Therapeutics Ireland Ltd.
- SwedenTegsedi 284 mg Injektionsvätska, lösning i förfylld sprutaAkcea Therapeutics Ireland Ltd
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tegsedi
- Liechtenstein · Tegsedi
- Norway · Tegsedi
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 Base de données publique des médicaments — BDPM (France). 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/aa9f57bc-ac58-472c-9a20-c61c5f8dfa0e GET /v1/drugs/aa9f57bc-ac58-472c-9a20-c61c5f8dfa0e?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.
{
"cis": "60789511",
"date_amm": "2018-07-06",
"type_amm": "Procédure centralisée",
"numero_ue": "EU/1/18/1296",
"substance": "INOTERSEN SODIQUE",
"atc_source": "fr_atc_restore_2026-09-06",
"statut_amm": "Autorisation active",
"statut_bdm": null,
"forme_pharmaceutique": "solution injectable",
"voies_administration": "sous-cutanée",
"etat_commercialisation": "Commercialisée",
"surveillance_renforcee": "Non"
}See everything about inotersen.
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.