Glucagon dosage in published studies and labels

These are the doses used for Glucagon in FDA labelling and published clinical studies, reported as each source states them, one row per regimen. They describe what was studied or approved for a specific population. They are not a recommendation, and none of them is a dose for any individual.

Research and educational reference only. This is not medical advice, and no figure on this page is a dosing recommendation.

Last checked against primary sources:

Studied regimens and sources

Glucagon has FDA-approved human dosages for severe low blood sugar in people with diabetes. Injected glucagon is 1 mg for adults and for children weighing 20 kg or more, and 0.5 mg for children under 20 kg, given under the skin, into a muscle or into a vein. Gvoke is 1 mg under the skin from age 12 (0.5 mg for children aged 2 to under 12 who weigh less than 45 kg), and the Baqsimi nasal powder is a single 3 mg dose from age 1. Each label allows one more dose after 15 minutes if there is no response.

FDA Approved
Dosage evidence summary for Glucagon
Human dosing establishedYes
RouteSubcutaneous · Intramuscular · Intravenous · Intranasal
FrequencySingle emergency dose; one repeat after 15 minutes if there is no response
Duration studiedSingle use per episode
Evidence levelFDA Approved
Last reviewed2026-11-07

Research-reported dosing

Doses as studied, one row per regimen. Different trials used different regimens; they are listed separately rather than averaged.

Research-reported dosing for Glucagon, one row per studied regimen
Study / contextPopulationDoseRouteFrequencyDurationOutcome studiedSource
FDA label — Glucagon for Injection, severe hypoglycemiaFDA-approved label · FDA prescribing informationAdults and children with diabetes1 mg for adults and children weighing 20 kg or more; 0.5 mg (or 20–30 mcg/kg) for children under 20 kgSubcutaneous, intramuscular or intravenous (intravenous only under medical supervision)Once; one more dose after 15 minutes if there is no response—Treatment of severe hypoglycemiaGlucagon for Injection (Amphastar) — FDA prescribing information, DailyMed
FDA label — Glucagon for Injection, diagnostic aidFDA-approved label · FDA prescribing informationAdults having radiologic examinationsUsually 0.25–0.5 mg intravenously or 1 mg intramuscularly to relax the stomach and small bowel; up to 2 mg if requiredIntravenous or intramuscularOnce, before or during the examination—Temporary inhibition of gastrointestinal movementGlucagon for Injection (Amphastar) — FDA prescribing information, DailyMed
FDA label — GVOKE, severe hypoglycemiaFDA-approved label · FDA prescribing informationAdults and children aged 2 and over with diabetes1 mg from age 12; ages 2 to under 12: 0.5 mg under 45 kg, 1 mg at 45 kg or moreSubcutaneousOnce; one more dose from a new device after 15 minutes if there is no response—Treatment of severe hypoglycemiaGVOKE (glucagon injection) — FDA prescribing information, DailyMed
FDA label — BAQSIMI nasal powder, severe hypoglycemiaFDA-approved label · FDA prescribing informationAdults and children aged 1 year and older with diabetes3 mg as one actuation into one nostrilIntranasalOnce; one more 3 mg dose after 15 minutes if there is no response—Treatment of severe hypoglycemiaBAQSIMI (glucagon) nasal powder — FDA prescribing information, DailyMed

Where sources disagree

  • Glucagon is an emergency medicine for severe hypoglycemia and a diagnostic aid for imaging. The labels call for emergency help right after a dose and oral carbohydrate once the person responds.
  • Doses are not interchangeable between forms: the nasal powder dose is 3 mg, while injected doses are 0.5 mg or 1 mg.