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France· FR:62170212

KADCYLA 100 mg, poudre pour solution à diluer pour perfusion

A trastuzumab emtansine product containing trastuzumab emtansine, registered in France by ROCHE REGISTRATION (ALLEMAGNE). The same ATC class is registered in 14 of our 19 countries.

ATC L01FD03

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedKADCYLA 100 mg, poudre pour solution …ATCL01FD03REGISTER NO.FR:62170212PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Trastuzumab emtansine is registered in 14 of 19 countries.

Countries holding a registration under ATC L01FD03 (trastuzumab emtansine), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 9 of them publish a price we can compare per daily dose

Trastuzumab emtansine · ATC L01FD03

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

Price per daily dose

What a daily dose of trastuzumab emtansine costs, country by country.

Normalised to the WHO defined daily dose (12 mg), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Trastuzumab emtansine · price per daily dose (12 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$237.25
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
TRASTUZUMAB EMTANSINE
Manufacturer
ROCHE REGISTRATION (ALLEMAGNE)
Country
France (FR)
ATC code
L01FD03
ATC class
Trastuzumab emtansine
Defined daily dose
12 mg, P
Reimbursed
No
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

  • cip13
    3400958576041
    1 flacon(s) en verre de 15 ml

Regulatory notes

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

Interactions

256 interactions on record for trastuzumab emtansine.

Graded by severity as the source publishes them — 62 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

Trastuzumab emtansine · interactions on record

256 records

  • 62 severe
  • 194 moderate

Most severe, free to view

  • DicoumarolB01AA01severe
  • WarfarinB01AA03severe
  • HeparinB01AB01severe
  • DalteparinB01AB04severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Trastuzumab emtansine in 15 other countries

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

All trastuzumab emtansine products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Kadcyla
  • Liechtenstein · Kadcyla
  • Norway · Kadcyla

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/fdb61f2f-1a6e-47ea-88ee-fce5ec7d3f18
GET /v1/drugs/fdb61f2f-1a6e-47ea-88ee-fce5ec7d3f18?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": "62170212",
  "date_amm": "2013-11-15",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/13/885",
  "substance": "TRASTUZUMAB EMTANSINE",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "poudre pour solution à diluer pour perfusion",
  "voies_administration": "intraveineuse",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about trastuzumab emtansine.

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.