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Netherlands· NL-32293575baf8

Somavert 30 mg, poeder en oplosmiddel voor oplossing voor injectie

A pegvisomant product containing pegvisomant, registered in Netherlands by Pfizer Europe MA EEIG. The same ATC class is registered in 14 of our 19 countries.

ATC H01AX01

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedSomavert 30 mg, poeder en oplosmiddel…ATCH01AX01REGISTER NO.NL-32293575baf8PACKS LISTED1CHECKEDSeptember 29, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about pegvisomantAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Pegvisomant is registered in 14 of 19 countries.

Countries holding a registration under ATC H01AX01 (pegvisomant), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 9 of them publish a price we can compare per daily dose
Search pegvisomant products by name

Pegvisomant · ATC H01AX01

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Italyprice
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
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 pegvisomant costs, country by country.

Normalised to the WHO defined daily dose (10 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
Open the full comparison — free accountDrug prices for market access

Pegvisomant · price per daily dose (10 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$81.23
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

CBG-MEB (Netherlands)
Active substance
PEGVISOMANT
Manufacturer
Pfizer Europe MA EEIG
Country
Netherlands (NL)
ATC code
H01AX01
ATC class
Pegvisomant
Defined daily dose
10 mg, P
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/02/240

Regulatory notes

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

Interactions

87 interactions on record for pegvisomant.

Graded by severity as the source publishes them — 87 moderate. 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
Check pegvisomant against other medicinesHow interaction checks work

Pegvisomant · interactions on record

87 records

  • 87 moderate

Most severe, free to view

  • OpiumA07DA02moderate
  • LiraglutidA08AX02moderate
  • SemaglutidA08AX03moderate
  • Insulin (human)A10AB01moderate
  • 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

Pegvisomant in 15 other countries

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

All pegvisomant products

Authorised across Europe · EMA

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

  • Iceland · Somavert
  • Liechtenstein · Somavert
  • Norway · Somavert

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 CBG-MEB (Netherlands). 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/e5857ec7-86d9-4726-b7a0-4808ae6cbbf0
GET /v1/drugs/e5857ec7-86d9-4726-b7a0-4808ae6cbbf0?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": "Poeder en oplosmiddel voor oplossing voor injectie",
  "route": "Subcutaan gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/somavert-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Pegvisomant",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp115448",
  "excipients": [
    "DINATRIUMWATERSTOFFOSFAAT 0-WATER (E 339)",
    "GLYCINE (E 640)",
    "MANNITOL (D-) (E 421)",
    "NATRIUMDIWATERSTOFFOSFAAT 1-WATER (E 339)",
    "STIKSTOF (HEAD SPACE) (E 941)",
    "WATER VOOR INJECTIE"
  ],
  "substances": [
    "PEGVISOMANT"
  ],
  "leaflet_url": null,
  "authorised_at": "2015/07/17",
  "procedure_number": "EMEA/H/C/000409",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/02/240",
  "additional_monitoring": "N"
}
API referenceMCP serverPlans

See everything about pegvisomant.

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.

Try it freeOpen in the console