Language
Austria

Available again · 27.08.2026

Supply shortage Austria: ZADENVI 60 mg Injektionslösung in einer Fertigspritze

Affected country: Austria · Reported period: 22.07.2026 – 04.09.2026 · Active ingredient: DENOSUMAB

CountryAustria
PZN6067962
ENRBASG-ID 0be473826b1ad26d540bc754a7675386914d3395; Zulassungsnummer EU/1/25/1937/001
Notification typeAvailable again
Start22.07.2026
Expected end04.09.2026
Last update27.08.2026
ReasonIncreased demand
ATCM05BX04
Hospital-relevantNo

Notice context

A supply shortage has been recorded for ZADENVI 60 mg Injektionslösung in einer Fertigspritze in Austria. The stated reason is “Increased demand”. The notice concerns the active ingredient DENOSUMAB 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: BASG – Medizinmarktaufsicht

Official shortage notice for Austria. 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 ZADENVI 60 mg Injektionslösung in einer Fertigspritze is a supply signal concerning DENOSUMAB in Austria. 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 ZADENVI 60 mg Injektionslösung in einer Fertigspritze 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.

Because the product name may indicate a temperature-sensitive dosage form, the product specification and any 2–8 °C requirement are assessed project by project; this is not a blanket capacity commitment.

Operational checks for this notice

  • Match product identity using PZN 6067962, active ingredient, strength, dosage form and pack.
  • Confirm the reported status and the period 22.07.2026 to 04.09.2026 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 ZADENVI 60 mg Injektionslösung in einer Fertigspritze:

Related topics