Glucagon
Also known as: GlucaGen, Baqsimi, Gvoke
Glucagon binds the hepatic glucagon receptor (GCGR), raising cyclic AMP to stimulate glycogenolysis and gluconeogenesis, which increases blood glucose as the body's main counter-regulatory hormone opposing insulin.
- Drug class
- Glucagon receptor (GCGR) agonist; counter-regulatory pancreatic hormone
- Primary targets
- Glucagon receptor (GCGR)
- Dose reference
- Reference (label, not a recommendation): 1 mg SC/IM/IV injectable for severe hypoglycemia in adults; Gvoke 0.5 mg pediatric / 1 mg adult SC; Baqsimi 3 mg single intranasal dose; 0.25-2 mg IV/IM as a GI diagnostic aid
- Half-life
- Short; roughly 8-18 minutes for native glucagon (pharmacokinetic studies)
- Developer / origin
- Eli Lilly (original glucagon and Baqsimi); Novo Nordisk (GlucaGen); Xeris (Gvoke)
- Reference year
- 1923
- Evidence score
- 5/5 - Strong
Strong
Glucagon is an FDA-approved rescue therapy for severe hypoglycemia with decades of label-backed clinical and pharmacokinetic evidence across injectable and intranasal forms.
Approved medication with substantial human clinical evidence.
Evidence basis
- FDA-approved prescribing information for GlucaGen, Gvoke and Baqsimi documents indication, dosing and safety
- Pharmacokinetic studies establish short half-life and rapid glucose response across IN/IM/IV routes
- Registration trials for Baqsimi and Gvoke demonstrated reliable reversal of insulin-induced hypoglycemia
How to read this entry
Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.
Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.
Glucagon guides
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