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EMA Product

Zegalogue

Product approved by European Medicines Agency (EU)

Basic Information

Zegalogue

Regulatory Information

EMEA/H/C/006214

Authorised

July 24, 2024

May 30, 2024

2

November 7, 2024

Company Information

Denmark

Novo Alle 1 DK-2880 Bagsvaerd

Novo Nordisk A/S

Drug Classification

Additional Monitoring

Active Substances Detail

dasiglucagon hydrochloride

Detailed Information

Therapeutic Indication

### Therapeutic indication Zegalogue is indicated for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 6 years and over with diabetes mellitus.

Overview Summary

Zegalogue is used for treating severe hypoglycaemia (low blood glucose levels) in adults and children from 6 years of age who have diabetes mellitus. Hypoglycaemia can occur when diabetes medicines cause glucose levels to fall too low. In severe cases, patients can faint or become unconscious, and they must be treated urgently to raise their glucose levels. Zegalogue contains the active substance dasiglucagon.

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