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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Glucagon

FDA approved · Rx

Pancreatic peptide hormone

Also known as: GlucaGen, Gvoke, Baqsimi, Gvoke Hypopen 0.5 Mg Auto-Injector, Gvoke Hypopen 1 Mg Auto-Injector, Gvoke Pfs 1 Mg Pre-Filled Syringe, Gvoke Kit, Gvoke Vialdx, Glucagonum, Glucagone

Evidence score
95/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 1521 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 2 cited sources. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Glucagon is a 29 amino acid peptide hormone made naturally by alpha cells in the pancreas. It raises blood sugar mainly by signaling the liver to break down stored glycogen and release glucose. It is sold as prescription products under names such as GlucaGen, Gvoke, and Baqsimi.

What the evidence shows

Automatic summaryHuman trials

Glucagon is FDA approved for the treatment of severe hypoglycemia, and some formulations are also approved for use as a diagnostic aid to temporarily slow gut movement during radiologic exams. It is backed by a very large body of human research, including more than 1,500 registered trials reaching Phase 4.

Key facts

Molecular formula
C153H225N43O49S
Molecular weight
3482.7 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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