Canada· CA-DIN-02468077
HAEGARDA
A c1-inhibitor, plasma derived product containing c1 esterase inhibitor (human), registered in Canada by CSL BEHRING CANADA INC. The same ATC class is registered in 11 of our 19 countries.
Checked against Health Canada Drug Product Database (Canada) on
Informational only — not a medical device.
Where it is registered
C1-inhibitor, plasma derived is registered in 11 of 19 countries.
Countries holding a registration under ATC B06AC01 (c1-inhibitor, plasma derived), each read from that country’s own register.
- This record: Canada, from Health Canada Drug Product Database (Canada)
- 7 of them publish a price we can compare per daily dose
C1-inhibitor, plasma derived · ATC B06AC01
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Health Canada Drug Product Database (Canada)- Active substance
- C1 ESTERASE INHIBITOR (HUMAN)
- Manufacturer
- CSL BEHRING CANADA INC
- Country
- Canada (CA)
- ATC code
- B06AC01
- ATC class
- C1-inhibitor, plasma derived
- Defined daily dose
- 1.4 TSD, E
- Reimbursed
- Not published by this register
- Source register
- Health Canada Drug Product Database (Canada)
- Last checked
- October 1, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
47 interactions on record for c1-inhibitor, plasma derived.
Graded by severity as the source publishes them — 5 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
C1-inhibitor, plasma derived · interactions on record
47 records
- 5 severe
- 42 moderate
Most severe, free to view
- CarfilzomibL01XG02severe
- CarfilzomibL01XX45severe
- ThalidomideL04AX02severe
- LenalidomideL04AX04severe
- 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
C1-inhibitor, plasma derived in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaBERINERTCSL Behring GmbH, Marburg
- United KingdomBerinert 1,500unit powder and solvent for solution for injection vialsCSL Behring UK Ltd
- BelgiumBerinert 2000 IUCSL Behring
- IrelandBerinert 1500 IU Powder and solvent for solution for injectionCSL Behring GmbH
- IcelandBerinertCSL Behring GmbH*
- NorwayBerinertCSL Behring GmbH (2)
- SwedenBerinert 1500 IE Pulver och vätska till injektionsvätska, lösningCSL Behring GmbH
- GermanyBerinertCsl Behring Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 30 EEA countries. Names it is sold under:
- Austria · Berinert
- Belgium · Berinert
- Bulgaria · Беринерт
- Cyprus · Berinert
- Czechia · Berinert
- Germany · Berinert
- Denmark · Berinert
- Estonia · Berinert Iv, Berinert Sc
- Spain · Berinert
- Finland · Berinert
- France · Berinert
- United Kingdom (Northern Ireland) · Berinert
- Greece · Berinert
- Croatia · Berinert
- Hungary · Berinert
- Ireland · Berinert
- Iceland · Berinert, Cinryze
- Italy · Berinert
- Liechtenstein · Cinryze
- Lithuania · Human C1-Esterase Inhibitor Csl Behring
- Luxembourg · Berinert
- Malta · Berinert
- Netherlands · Berinert
- Norway · Berinert, Cinryze
- Poland · Berinert
- Portugal · Berinert
- Romania · Berinert
- Sweden · Berinert
- Slovenia · Berinert
- Slovakia · Berinert
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 Health Canada Drug Product Database (Canada). 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/ca6e2031-fef9-47ec-aa70-fe23fad0af5b GET /v1/drugs/ca6e2031-fef9-47ec-aa70-fe23fad0af5b?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.
{
"din": "02468077",
"form": "KIT",
"class": "Human",
"routes": [
"SUBCUTANEOUS"
],
"source": "health_canada_dpd",
"status": "MARKETED",
"atc_raw": "B06AC01",
"schedule": [
"Schedule D"
],
"drug_code": "95644",
"strengths": [
"3000 UNIT"
],
"ahfs_class": null,
"substances": [
"C1 ESTERASE INHIBITOR (HUMAN)"
],
"product_categorization": null
}See everything about c1-inhibitor, plasma derived.
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.