FDA (US): Approved since 1960 (injectable) for severe hypoglycemia and as a diagnostic aid; newer formulations: Baqsimi (2019, nasal powder) and Gvoke (2019, ready-to-use solution).
EMA (EU): Approved: Baqsimi (2019, nasal) and Ogluo (2021, ready-to-use solution) for severe hypoglycemia; GlucaGen is authorized nationally in Spain and other countries.
Severe hypoglycemia: 1 mg injected (0.5 mg in young children) or 3 mg intranasally (Baqsimi), per label (FDA/EMA).
Beta-blockers (rise in heart rate and blood pressure), indomethacin (reduced effect), warfarin (greater anticoagulant effect).
In a phase 3 trial with 170 adults with type 1 diabetes (reference arm), 1 mg of reconstituted glucagon recovered glucose in a median of 12 minutes, vs 40 minutes with placebo.
View the study (RCT) →It activates its receptor in the liver to release stored glucose (glycogen) and make new glucose. It also relaxes the muscles of the digestive tract, which is why it is used in some radiological examinations.
In people
Information, not medical advice. Prescription or unapproved peptides should only be used under medical supervision.