Language
Belgium

Unavailable · 07.10.2026

Supply shortage Belgium: Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml

Affected country: Belgium · Reported period: 17.08.2026 – 30.11.2026 · Active ingredient: Tirofiban

Illustration of medicine supply and shortage monitoring in Europe – Supply shortage Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml | CNK 1506088
Illustration of medicine supply and shortage monitoring in Europe – Supply shortage Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml | CNK 1506088
CountryBelgium
CNK1506088
ENRFAMHP-ID 6a84bdd4abfc71120c81b209; BE205247
Notification typeUnavailable
Start17.08.2026
Expected end30.11.2026
Last update07.10.2026
ReasonIncreased demand
ATCB01AC17
Hospital-relevantNo

Notice context

A supply shortage has been recorded for Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml in Belgium. The stated reason is “Increased demand”. The notice concerns the active ingredient Tirofiban 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 Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml is a supply signal concerning Tirofiban in Belgium. The published reason “Increased demand” determines which data should be verified first.

When demand rises, available stock, open orders, allocations, actual stock coverage and the confirmed replenishment date should be checked separately.

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 allocations, coverage, replenishment and a lawful product-specific buffer stock separately.
  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

For demand peaks, a lawful, product-specific safety or buffer stock for Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml can support operational coverage.

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 1506088, active ingredient, strength, dosage form and pack.
  • Confirm the reported status and the period 17.08.2026 to 30.11.2026 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 Aggrastat 0.25 mg/ml inf. sol. (conc.) i.v. vial 50 ml:

Related topics