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Glucagon

GLUCAGEN

What it isGlucagon-receptor agonist raising hepatic glucose output; severe hypoglycemia and beta-blocker overdose.

Why this oneIt rescues hypoglycemia without oral or IV access and raises cAMP independently of beta receptors in beta-blocker overdose.

What limits itIt fails when hepatic glycogen is depleted, as in prolonged fasting or severe alcohol-related malnutrition; vomiting is common.

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Severe hypoglycemia (SubQ)Adults & peds ≥12 yr1 mg SubQ1 mg SubQ
Severe hypoglycemia (SubQ)Peds 2 to <12 yr0.5 mg (<45 kg) or 1 mg (≥45 kg) SubQ
Diagnostic aid — GI relaxation (IV, VialDx)Adults0.2–0.5 mg (stomach/duodenum) or 0.5–0.75 mg (colon) IV0.75 mg IV

Renal Undefined

Hepatic Undefined

May give one additional dose from a new device after 15 minutes if no response

Instructions

Contraindications

Cautions

Adverse reactions

Pregnancy Data over decades show no drug-associated risk; minimal placental transfer.

Lactation No data; as a peptide, unlikely to harm a breastfed infant (broken down in the infant's GI tract).

NO BOXED WARNINGS

Principal riskIt fails without hepatic glycogen

Cost, est. cash$300–$5,000/dose or month

Generic entry2020

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk1 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

Mechanism of action: Glucagon ballicule

Glucagon ballicule: receptor binding, kinetics and half-life diagram

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