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💊 Medicine EU 23 marzo 2026

Eli Lilly insulin (various forms)

📷 EU Safety Watch placeholder
Eli Lilly insulin (various forms)
📷 EU Safety Watch placeholder
L'Insulina Eli Lilly (in varie forme) Forme: soluzione iniettabile; sospensione iniettabile. Alternative: sì.
⚠️
Shortage ongoing
è attualmente carente in EU.
📈 Cronologia
13 giorni attivo finora
16 maggio 2026 28 maggio 2026

What is this? This is insulin made by Eli Lilly. It comes as a liquid or a mix you inject under the skin.

What's happening? Some forms of this insulin are in short supply right now.

Does this affect me? If you use Eli Lilly insulin, you may be affected.

What should I do? Talk to your pharmacist or doctor before changing your dose or brand.

🤖 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
23/03/2026
Farmaci interessati
Eli Lilly insulin (various forms)
Stato di carenza di fornitura
Ongoing
Disponibilità di alternative
Yes
Forme farmaceutiche interessate
Solution for injectionSuspension for injection

Contenuti della pagina

Informazioni sulla carenza

Eli Lilly is discontinuing some of its insulin presentations (containing human insulin, insulin lispro and insulin glargine) across selected countries. The specific products affected and the timelines for their withdrawal differ across EU/EEA countries. All discontinuations are expected to occur before Q2 2027, after which the affected insulin presentations will no longer be available.

This is in addition to Humalog Mix25 (25% insulin lispro and 75% insulin lispro protamine, 100 units/ml suspension for injection, vial) which has already been discontinued in all EU/EEA countries where it was marketed.

Insulin medicines are used to treat patients who have diabetes and need insulin to help control their blood glucose (sugar) level.

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

For more details and up-to-date information on the availability of individual insulins, consult your country’s shortage register or contact your national competent authority. 

The company Eli Lilly has decided to stop marketing some of its insulin medicines for commercial reasons. This decision is not related to a quality defect or safety issue. 

The discontinuations affect Member States differently. 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.

  • For information specific to your country, please consult your national shortage register or contact your national competent authority.
  • In affected Member States, healthcare professionals will receive a shortage communication letter with details on the impacted insulins and recommended actions.
  • Where applicable, healthcare professionals should transition patients currently using any of the affected insulins to suitable alternatives, in line with existing guidance and their clinical judgement.
  • 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.
  • Healthcare professionals may also contact relevant organisations for further information. A list of European not-for-profit organisations EMA engages with can be found on the EMA website.

  • For information specific to your country, please consult your national shortage register or contact your healthcare professional.
  • 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.
  • If 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.
  • If 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, as you may be at 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 Eli Lilly has decided to stop marketing some of its insulin medicines for commercial reasons. This decision is not related to a quality defect or safety issue. 

Stati membri interessati

The discontinuations affect Member States differently. 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

  • For information specific to your country, please consult your national shortage register or contact your national competent authority.
  • In affected Member States, healthcare professionals will receive a shortage communication letter with details on the impacted insulins and recommended actions.
  • Where applicable, healthcare professionals should transition patients currently using any of the affected insulins to suitable alternatives, in line with existing guidance and their clinical judgement.
  • 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.
  • Healthcare professionals may also contact relevant organisations for further information. A list of European not-for-profit organisations EMA engages with can be found on the EMA website.

Raccomandazioni per pazienti e caregiver

  • For information specific to your country, please consult your national shortage register or contact your healthcare professional.
  • 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.
  • If 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.
  • If 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, as you may be at 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
Eli Lilly insulin (various forms)
Supply shortage status
Ongoing
Pharmaceutical forms affected
  • Solution for injection
  • Suspension for injection
Availability of alternatives
Yes

Date chiave

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
Marca(e) / nome(i) del prodotto
Dettaglio pubblicato dall'ente

Forms: Solution for injection;Suspension for injection · Alternatives: Yes

Prima pubblicazione
23 marzo 2026
Ultimo aggiornamento da noi
1 settimana fa
Gravità (classificata)
Medio
Fonte ufficiale
https://www.ema.europa.eu/en/medicines/human/shortages/eli-lilly-insulin-various-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?
Eli Lilly insulin (various forms). L'Insulina Eli Lilly (in varie forme) Forme: soluzione iniettabile; sospensione iniettabile. Alternative: sì.
Quando è stata emessa questa allerta?
Questo avviso è stato emesso il 23 marzo 2026 da EMA (European Medicines Agency).
Quali paesi sono interessati?
L'avviso si applica a l'intera UE.
Quanto è grave questo avviso?
:severità. A medium risk means harm is possible under certain conditions. Read the notice and act on the recommended steps.
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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