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💊 Medicine EU 31 ottobre 2025

NovoNordisk insulin (human insulin) (various short-, rapid-, intermediate-, mixed- and long-acting forms)

📷 EU Safety Watch placeholder
NovoNordisk insulin (human insulin) (various short-, rapid-, intermediate-, mixed- and long-acting forms)
📷 EU Safety Watch placeholder
L'insulina NovoNordisk (insulina umana) è disponibile in varie forme: a breve, rapida, intermedia, mista e ad azione prolungata. Si presenta come soluzione o sospensione iniettabile con una concentrazione di 100 unità/ml. Esistono alternative.
⚠️
Shortage ongoing
è attualmente carente in EU.
📈 Cronologia
12 giorni attivo finora
16 maggio 2026 27 maggio 2026

What is this? This is insulin made by NovoNordisk. It comes as a liquid or cloudy mix you inject. It helps control blood sugar for people with diabetes.

What's happening? Some types of this insulin are hard to find right now in the EU. Supplies are running low.

Does this affect me? If you use this insulin, you may have trouble getting your usual supply.

What should I do? Talk to your pharmacist or doctor before you run out. They can suggest another insulin or help you get what you need.

🤖 Questo riassunto in linguaggio semplice viene generato automaticamente dalla notifica ufficiale dell'agenzia tramite IA. È solo a scopo informativo generale — non è un consiglio medico. Per decisioni relative alla tua salute, consulta sempre un farmacista o un medico e leggi la fonte ufficiale collegata di seguito.

📋 Dalla comunicazione ufficiale dell'ente

Aggiornato 1 settimana fa
Prima pubblicazione
31/10/2025
Farmaci interessati
NovoNordisk insulin (human insulin) (various short-, rapid-, intermediate-, mixed- and long-acting forms)
Punti di forza interessati
100 units/ml
Risoluzione prevista
End of 2026
Stato di carenza di fornitura
Ceased
Disponibilità di alternative
Yes
Forme farmaceutiche interessate
Solution for injectionSuspension for injection

Contenuti della pagina

Informazioni sulla carenza

The company Novo Nordisk has decided to stop marketing some of selected presentations of insulins due to commercial reasons:

  • short- and rapid-acting (bolus/mealtime) insulins (human insulin, 100 units/ml, solution for injection),
  • intermediate-acting (isophane) insulins (NPH human insulin, 100 units/ml, solution for injection),
  • mixed-acting (biphasic) insulins (suspension for injection) and
  • long-acting (basal) insulins (solution for injection in pre-filled pen).

These insulins will be discontinued in all Member states where they were previously marketed and will therefore be unavailable.

The table below provides further details on the insulins that are being discontinued.  

The listed products/ presentations are not marketed in all EU/EEA countries. However, where they are marketed they will be discontinued.

For more details and up-to-date information, consult your country’s shortage register or contact your national competent authority.

For information on the use of the medicines please refer to the respective medicine overview pages on EMA’s website.

Products Presentation(s) subject to discontinuation
Short- and rapid-acting insulins
Actrapid (regular human insulin, 100 units/ml, solution for injection)  

Penfill

Flexpen

Innolet 

Short- and rapid-acting insulins
Fiasp (fast-acting insulin aspart, 100 units/ml, solution for injection) 
Pumpcart
Intermediate-acting insulins 
Insulatard (insulin NPH, 100 units/ml, suspension for injection in cartridge) 

Penfill

Flexpen

Innolet 

Intermediate-acting insulins 
Protaphane (isophane/NPH human insulin, 100 units/ml, suspension for injection in cartridge) 

Penfill

Flexpen

Mixed-acting (biphasic) insulins
Mixtard 30 (30% soluble insulin and 70% isophane insulin, 100 units/ml, suspension for injection in cartridge or pre-filled pen) 

Penfill

Flexpen

Innolet

Mixed-acting (biphasic) insulins
Mixtard 50 (50% soluble insulin and 50% isophane insulin, 100 units/ml, suspension for injection in cartridge or pre-filled pen) 
Penfill
Mixed-acting (biphasic) insulins
Actraphane 30 (30% soluble insulin and 70% isophane insulin, 100 units/ml, suspension for injection in cartridge or pre-filled pen) 

Penfill

Flexpen

Mixed-acting (biphasic) insulins
Actraphane 50 (50% soluble insulin and 50% isophane insulin, 100 units/ml, suspension for injection in cartridge or pre-filled pen) 

Penfill

Flexpen

Mixed-acting (biphasic) insulins
NovoMix 50 (50% insulin aspart and 50% insulin aspart protamine 100 units/ml, suspension for injection in cartridge or pre-filled pen) 

Penfill

Flexpen

Long-acting insulins
Levemir (insulin detemir 100 units/ml, solution for injection, in cartridge or pre-filled pen) 

Penfill

Flexpen

Innolet

Flextouch

The company Novo Nordisk has decided to stop marketing some of its insulins for commercial reasons. This decision is not related to a quality defect or safety issue.

The timeline for the discontinuation varies between Member States and discontinuation will take effect before the end of 2026. After this date the listed insulins will no longer be available.

All Member States where the listed presentations were marketed are affected by the discontinuations and the presentations will no longer be available. In addition, there may be intermittent shortages in some Member States before the discontinuation.

For more details, consult your country’s shortage register or contact your national competent authority. 

EMA’s Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) and EMA’s shortages working party (Medicines Shortages Single Point of Contact – SPOC - working party) are closely monitoring the supply situation and engaging with the marketing authorisation holder and other stakeholders to mitigate the impact of the planned discontinuations.

The SPOC Working Party Supports EMA’s MSSG and monitors and reports events that could affect the supply of medicines in the EU.

  • In the affected Member States healthcare professionals will receive a letter (medicine shortage communication) to provide details and recommendations.
  • No new patients should be started on any of the above listed insulins.
  • Healthcare professionals should switch any patients who are currently on any of the above listed insulins to alternative insulins based on existing guidance and clinical judgment.
  • Healthcare professionals should ensure that all patients are counselled on any changes in the new insulin regimen including the need to change dose and/or usage of the new insulin delivery system and additional glucose monitoring.
  • Close glucose monitoring is recommended when the patient is switched to another type or brand of insulin and in the initial weeks thereafter, especially in pregnant women and children who may need closer monitoring than the general population. The risk of hypoglycaemia may be higher in these populations.
  • A medicine shortage communication (MSC) has been sent to healthcare professionals in affected Member States.
  • You may also contact relevant healthcare professional organisations for further information. A list of European not-for-profit organisations EMA engages with can be found on the EMA website.
  • For additional information, consult your country’s shortage register or contact your national competent authority.

  • Contact your healthcare professional before your current supply of insulin runs out.
  • Your healthcare professional will advise you if any of the insulins you are using are affected by the discontinuation and will switch you to an alternative insulin, if needed.
  • In case your healthcare professional switches your insulin they will explain any changes to you and ensure that you are given adequate training on using any new insulin delivery system.
  • In case you are being switched you may need to closely monitor your glucose levels during the transfer to another type or brand of insulin and in the initial weeks thereafter. This applies especially if you are pregnant or under 18 years of age in which case you are at a higher risk of hypoglycaemia.
  • If you have any questions, speak to your doctor or pharmacist.
  • You may also contact relevant patients’ organisations for further information or support. A list of European not-for-profit organisations that EMA engages with can be found on the EMA website.
  • For additional information, consult your country’s shortage register or contact your national competent authority. 

Motivo della carenza

The company Novo Nordisk has decided to stop marketing some of its insulins for commercial reasons. This decision is not related to a quality defect or safety issue.

The timeline for the discontinuation varies between Member States and discontinuation will take effect before the end of 2026. After this date the listed insulins will no longer be available.

Stati membri interessati

All Member States where the listed presentations were marketed are affected by the discontinuations and the presentations will no longer be available. In addition, there may be intermittent shortages in some Member States before the discontinuation.

For more details, consult your country’s shortage register or contact your national competent authority. 

Monitoraggio della carenza

EMA’s Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) and EMA’s shortages working party (Medicines Shortages Single Point of Contact – SPOC - working party) are closely monitoring the supply situation and engaging with the marketing authorisation holder and other stakeholders to mitigate the impact of the planned discontinuations.

The SPOC Working Party Supports EMA’s MSSG and monitors and reports events that could affect the supply of medicines in the EU.

Raccomandazioni per gli operatori sanitari

  • In the affected Member States healthcare professionals will receive a letter (medicine shortage communication) to provide details and recommendations.
  • No new patients should be started on any of the above listed insulins.
  • Healthcare professionals should switch any patients who are currently on any of the above listed insulins to alternative insulins based on existing guidance and clinical judgment.
  • Healthcare professionals should ensure that all patients are counselled on any changes in the new insulin regimen including the need to change dose and/or usage of the new insulin delivery system and additional glucose monitoring.
  • Close glucose monitoring is recommended when the patient is switched to another type or brand of insulin and in the initial weeks thereafter, especially in pregnant women and children who may need closer monitoring than the general population. The risk of hypoglycaemia may be higher in these populations.
  • A medicine shortage communication (MSC) has been sent to healthcare professionals in affected Member States.
  • You may also contact relevant healthcare professional organisations for further information. A list of European not-for-profit organisations EMA engages with can be found on the EMA website.
  • For additional information, consult your country’s shortage register or contact your national competent authority.

Raccomandazioni per pazienti e caregiver

  • Contact your healthcare professional before your current supply of insulin runs out.
  • Your healthcare professional will advise you if any of the insulins you are using are affected by the discontinuation and will switch you to an alternative insulin, if needed.
  • In case your healthcare professional switches your insulin they will explain any changes to you and ensure that you are given adequate training on using any new insulin delivery system.
  • In case you are being switched you may need to closely monitor your glucose levels during the transfer to another type or brand of insulin and in the initial weeks thereafter. This applies especially if you are pregnant or under 18 years of age in which case you are at a higher risk of hypoglycaemia.
  • If you have any questions, speak to your doctor or pharmacist.
  • You may also contact relevant patients’ organisations for further information or support. A list of European not-for-profit organisations that EMA engages with can be found on the EMA website.
  • For additional information, consult your country’s shortage register or contact your national competent authority. 

Fatti principali

Medicines affected
NovoNordisk insulin (human insulin) (various short-, rapid-, intermediate-, mixed- and long-acting forms)
Supply shortage status
Ceased
Pharmaceutical forms affected
  • Solution for injection
  • Suspension for injection
Strengths affected
100 units/ml
Availability of alternatives
Yes

Date chiave

Expected resolution
End of 2026
First published

Informazioni correlate sulla salute

Il contenuto sopra è riprodotto dalla pagina ufficiale dell'ente (link sotto). Non lo modifichiamo, interpretiamo o aggiungiamo informazioni.
🔬 Dettagli medici/tecnici Per professionisti
Dettaglio pubblicato dall'ente

Forms: Solution for injection;Suspension for injection · Strengths: 100 units/ml · Alternatives: Yes

Prima pubblicazione
31 ottobre 2025
Ultimo aggiornamento da noi
17 ore fa
Gravità (classificata)
Alto
Fonte ufficiale
https://www.ema.europa.eu/en/medicines/human/shortages/novonordisk-insulin-human-insulin-various-short-rapid-intermediate-mixed-long-acting-forms

Tutte le informazioni su questa pagina provengono dal comunicato ufficiale dell'agenzia. Le traduciamo e le riassumiamo; non aggiungiamo né modifichiamo i fatti.

Avvisi correlati

❓ Domande frequenti

Di che tipo di avviso si tratta?
NovoNordisk insulin (human insulin) (various short-, rapid-, intermediate-, mixed- and long-acting forms). L'insulina NovoNordisk (insulina umana) è disponibile in varie forme: a breve, rapida, intermedia, mista e ad azione prolungata. Si presenta come soluzione o sospensione iniettabile con una concentrazione di 100 unità/ml. Esistono alternative.
Quando è stata emessa questa allerta?
Questo avviso è stato emesso il 31 ottobre 2025 da EMA (European Medicines Agency).
Quali paesi sono interessati?
L'avviso si applica a l'intera UE.
Quanto è grave questo avviso?
:severità. A serious risk means the product or medicine can cause significant harm. Treat the alert as urgent.
Cosa devo fare?
If you take this medicine, contact your pharmacist or prescribing doctor. They can advise on alternative products or substitutes. Do not stop taking prescription medicine without medical advice.
Dove posso trovare l'avviso ufficiale?
L'avviso ufficiale completo è pubblicato su www.ema.europa.eu.

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