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Poland· PL-100019108

Dihydroergotaminum Filofarm

A dihydroergotamine product containing dihydroergotamini mesilas, registered in Poland by Farmaceutyczna Spółdzielnia Pracy FILOFARM. The same ATC class is registered in 8 of our 19 countries.

ATC N02CA01

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedDihydroergotaminum FilofarmATCN02CA01REGISTER NO.PL-100019108PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Dihydroergotamine is registered in 8 of 19 countries.

Countries holding a registration under ATC N02CA01 (dihydroergotamine), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 6 of them publish a price we can compare per daily dose

Dihydroergotamine · ATC N02CA01

8 / 19 countries

  • Belgiumprice
  • Canada
  • Finlandprice
  • Franceprice
  • Norwayprice
  • Polandprice
  • 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.

The record

At a glance

URPL (Poland)
Active substance
Dihydroergotamini mesilas
Manufacturer
Farmaceutyczna Spółdzielnia Pracy FILOFARM
Country
Poland (PL)
ATC code
N02CA01
ATC class
Dihydroergotamine
Defined daily dose
1 mg, N
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    05909990211418

Regulatory notes

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

Interactions

178 interactions on record for dihydroergotamine.

Graded by severity as the source publishes them — 54 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

Dihydroergotamine · interactions on record

178 records

  • 54 severe
  • 90 moderate
  • 1 minor
  • 17 info

Most severe, free to view

  • EpinephrineA01AD01severe
  • IsomethepteneA03AX10severe
  • FenfluramineA08AA02severe
  • DexfenfluramineA08AA04severe

16 more interactions with mechanism and management, from a commercially licensed source.

Sign in to check
  • 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

Dihydroergotamine in 8 other countries

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

All dihydroergotamine products

Authorised across Europe · EMA

The same active substance is authorised in 7 EEA countries. Names it is sold under:

  • Austria · Dihydergot, Migranal
  • Belgium · Diergo Spray
  • France · Diergospray
  • United Kingdom (Northern Ireland) · Migranal
  • Greece · Dihydergot
  • Italy · Diidergot, Dineza
  • Sweden · Orstanorm

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 URPL (Poland). 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/c7e0a275-e7e7-488c-bb84-268ad81804a4
GET /v1/drugs/c7e0a275-e7e7-488c-bb84-268ad81804a4?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.

{
  "form": "Roztwór doustny",
  "source": "urpl",
  "strength": "2 mg/g",
  "packaging": "05909990211418 ¦ Rp ¦ 51333\n1 butelka 15 g",
  "substance": "Dihydroergocristini mesylas 0.03 g",
  "common_name": "Dihydroergotamini mesilas",
  "pl_product_id": "100019108",
  "pozwolenie_nr": "02114",
  "auth_procedure": "NAR",
  "authorisation_validity": "Bezterminowe"
}

See everything about dihydroergotamine.

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.