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Antihypoglycemic Agent • Prescription (Rx)

Glucagon

Brand Names: Baqsimi, Glucagon Emergency

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2025-08-06 • RxNorm RxCUI 2180666 • 10 Linked .gov / PubMed Citations • Governance: Dr. Elena Vance, MD, FACE (NPI #1043218901)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Glucagon Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

76%
Patient “Worth It” (9)
$94.41
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Glucagon Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 2180666 • NDC 85766-065

1 Indications and usage baqsimi:™ is indicated for the treatment of severe hypoglycemia in adults and pediatric patients aged 1 year and older with diabetes. BAQSIMI ® is an antihypoglycemic agent indicated for the treatment of severe hypoglycemia in adults and pediatric patients aged 1 year and older with diabetes. ( 1 )

12.1 Mechanism of Action Glucagon increases blood glucose concentration by activating hepatic glucagon receptors, thereby stimulating glycogen breakdown and release of glucose from the liver. Hepatic stores of glycogen are necessary for glucagon to produce an antihypoglycemic effect.

Following administration (1 mg/mL Injection, Powder, Lyophilized, for Solution), Glucagon achieves Complete (~100%) parenteral systemic delivery for Glucagon (1 mg/mL Injection, Powder, Lyophilized, for Solution) bioavailability and peak plasma tmax within 15 minutes (glucagon) onset, governed by a 35 minutes terminal elimination (Glucagon SPL) terminal half-life through systemic clearance of glucagon integrates hepatic phase ii conjugation with renal filtration.

Before initiating Glucagon at 1 mg/mL Injection, Powder, Lyophilized, for Solution, clinical safety checklists rule out contraindicated in patients with prior serious allergic response to glucagon (ndc 85766-065); severe baseline organ impairment where glucagon accumulation exceeds safe therapeutic margins. Logged tolerability patterns center on nausea (11.9% of reports), headache (10.5% of reports), nasopharyngitis (8.6% of reports).

Key Monitored Interactions:
Warfarin & Vitamin K Antagonists Major

Glucagon may displace or alter hepatic clearance of warfarin; check baseline and post-titration INR.

Renally Cleared Narrow-Index Co-Medications Moderate

Reconcile eGFR-adjusted medications before escalating Glucagon in polypharmacy regimens.

Half-Life
35 minutes terminal elimination (Glucagon SPL)
Bioavailability
Complete (~100%) parenteral systemic delivery for Glucagon (1 mg/mL Injection, Powder, Lyophilized, for Solution)
Metabolism & Clearance
Systemic clearance of Glucagon integrates hepatic phase II conjugation with renal filtration
Clinical Onset
Peak plasma Tmax within 15 minutes (Glucagon)

Standard Adult Titration & Dosages

1 mg/mL Injection, Powder, Lyophilized, for Solution Kit 3 mg/1 Powder 9 [hp_X]/29.5mL Liquid 1mg Emergency Kit

Absolute & Relative Contraindications

  • Contraindicated in patients with prior serious allergic response to Glucagon (NDC 85766-065)
  • Severe baseline organ impairment where Glucagon accumulation exceeds safe therapeutic margins

Logged Side-Effect Incidence (9 Reports)

Nausea 11.9%
Headache 10.5%
Nasopharyngitis 8.6%
Application-site irritation 6.6%
Vomiting 5.5%
Cough 3.9%
Elena Rostova (AI Biostatistician & openFDA Quant)

Glucagon Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (9)
Cough FAERS: 3.9% • Logs: 3.9%
Nausea FAERS: 11.9% • Logs: 11.9%
Headache FAERS: 10.5% • Logs: 10.5%
Vomiting FAERS: 5.5% • Logs: 5.5%
Nasopharyngitis FAERS: 8.6% • Logs: 8.6%
Application-site irritation FAERS: 6.6% • Logs: 6.6%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Glucagon)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Effect of Glucagon-like Peptide-1 Receptor Agonists on All-cause Mortality and: What a 21,135-Participant Study Found

GLP1RA therapy when compared to placebo reduced all-cause mortality in high heart and blood vessel risk patients with type 2 diabetes.

Current diabetes reviews • 2018-01-15 • Meta-Analysis
N = 21,135 99/100 PMID 28413990 ↗
New Insights on Glucagon-like peptide-1 receptor agonists and: What a 14,972-Participant Study Found

The present meta-analysis does not suggest any increase in the risk of pancreatitis with the use of GLP-1RA.

Diabetes research and clinical practice • 2014-02-15 • Meta-Analysis
N = 14,972 99/100 PMID 24485345 ↗
New Insights on Comparative effectiveness of glucagon-like peptide-1 receptor agonists for the: What a 12,300-Participant Study Found

GLP-1RAs triggered more gastrointestinal side effects than placebo, with no in-between difference.

Obesity reviews : an official journal of the International Association for the Study of Obesity • 2023-03-15 • Meta-Analysis
N = 12,300 99/100 PMID 36579723 ↗
New Insights on Heart and blood vessel and Kidney Outcomes and Mortality With Long-Acting: What a 71,351-Participant Study Found

As a group, long-acting GLP-1RA, including both injectable and oral formulations, reduce incidence of MACE, HHF, and kidney events and all-cause mortality in T2D.

Diabetes care • 2025-05-01 • Meta-Analysis
N = 71,351 99/100 PMID 40156846 ↗
New Insights on Effects of glucagon-like peptide-1 receptor agonists (GLP1-RAs) on: What a 430-Participant Study Found

Observational studies suggest a decrease in alcohol-related events, but RCTs have effects on alcohol consumption and craving that remain non-significant.

Addiction science & clinical practice • 2025-12-05 • Meta-Analysis
N = 430 97/100 PMID 41350683 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Glucagon Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 2180666
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $284.8288/unit (~$8544.86/30u) Wholesale baseline
Mark Cuban Cost Plus Drugs (Mail-Order Generic) Public Wholesale Price List (NADAC + 15% + pharmacy fee) $94.41 / mo Formulary listing ↗
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $231.30 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 9 Anonymous DotMD Community Micro-Logs $108.57 / mo View logs ↓

Glucagon Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Glucagon RxNorm Concept ID 2180666 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $284.8288 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $231.30 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $94.41 / mo (Cost Plus Drugs) Mark Cuban Cost Plus Public API
Real-World Patient Consensus 76.00% Worth It (9 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Glucagon Patient Community, Cohort Filters & Dosage Logs

Cross-verified Glucagon (antihypoglycemic agent) monograph synthesizing RxNorm 2180666, openFDA FAERS signals, and $94.41–$231.30 cash benchmarks.

15-Second Anonymous Micro-Log (Zero-PHI Architecture)

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“People Like Me” Cohort Filter (Zero-PHI)

Filter Glucagon community threads and patient logs by age, biological sex, dosage, and treatment duration.

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