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Belgium

Unavailable · 23.09.2026

Supply shortage Belgium: ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml

Affected country: Belgium · Reported period: 07.04.2026 – 31.12.2026 · Active ingredient: Moroctocog Alfa

Illustration of medicine supply and shortage monitoring in Europe – Supply shortage ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml | CNK 3026234
Illustration of medicine supply and shortage monitoring in Europe – Supply shortage ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml | CNK 3026234
CountryBelgium
CNK3026234
ENRFAMHP-ID 69d4f8a8329b076ed46f919d; EU/1/99/103/009
Notification typeUnavailable
Start07.04.2026
Expected end31.12.2026
Last update23.09.2026
ReasonOther
ATCB02BD02
Hospital-relevantNo

Notice context

A supply shortage has been recorded for ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml in Belgium. The stated reason is “Other”. The notice concerns the active ingredient Moroctocog Alfa and is not identified as hospital-relevant.

This information describes the reported supply status and is not medical or pharmaceutical treatment advice. Availability, alternatives and further measures must be assessed for each individual case by the responsible pharmaceutical market participants.

Primary source: FAMHP / FAGG-AFMPS – PharmaStatus

Official shortage notice for Belgium. Responsibility and update procedures follow the information supplied by the relevant authority.

Check the official notice list →

Implications for procurement and the supply chain

The notice for ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml is a supply signal concerning Moroctocog Alfa in Belgium. The published reason “Other” determines which data should be verified first.

Because the published reason does not establish a reliable operational cause, availability, source, timing, product status and the supply route should be verified without adding an unsupported explanation.

Decision route for this supply case

  1. Confirm the notice, product identity, period and actual demand with the primary source and accountable market participants.
  2. Assess source, product status, timing, lawful sourcing route and any buffer stock without adding an unsupported cause.
  3. Document release, stock status, GDP evidence, warehousing and transport process, and escalation responsibility.

Inter-Pharma can structure the B2B case, potential sourcing and warehousing routes, and operational implementation. Clinical decisions, regulatory permissibility, product release and actual availability remain with the accountable parties.

Request a structured supply review →

Operational shortage resilience: GDP warehousing and pharmaceutical storage

A resilient stock concept for ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml requires prior verification of product status, demand, coverage and the permitted supply route.

Inter-Pharma combines GDP-oriented pharmaceutical storage in Czechia with batch and expiry control, FEFO, stock status, picking and dispatch preparation in its own Cheb operation.

Storage at 15–25 °C or any 2–8 °C requirement is derived solely from the product specification and confirmed for the project.

Operational checks for this notice

  • Match product identity using CNK 3026234, active ingredient, strength, dosage form and pack.
  • Confirm the reported status and the period 07.04.2026 to 31.12.2026 with the primary source and potential suppliers.
  • Document demand, stock coverage, open orders and lawful alternative or sourcing routes for the specific case.
  • Clarify temperature, batch, expiry, stock status, recipient authorisation and GDP evidence before cross-border supply.

Relevant services and specialist pages

The following B2B topics are particularly relevant when handling a shortage involving ReFacto AF 250 IU inj. sol. (pwdr. + solv.) i.v. pre-filled syr. 250 IU + 4 ml:

Related topics