Evidence review: Open Peptide Project (verified against primary PubMed, ClinicalTrials.gov & FDA records) · Last checked 2026-10-27. ← Back to Evidence Library
Glucagon (Gvoke, Baqsimi, generics): what the evidence says
At a glance
What it is: a 29-amino-acid hormone from the pancreas that raises blood sugar. Synthetic versions are approved for severe hypoglycemia, as injections (e.g. Gvoke, Sep 2019) and a nasal powder (Baqsimi, Jul 2019), and as a diagnostic aid to relax the gut during imaging. R1, R2, R3, R4
What the evidence says: Human glucagon reliably reverses severe low blood sugar; a meta-analysis of 8 RCTs found nasal and injected glucagon similarly effective. R5 Newer weight-loss drugs (survodutide, mazdutide, retatrutide) add glucagon-receptor activity to GLP-1, but they are different molecules. R6, R7, R8
Biggest risks: nausea and vomiting are common. It must not be used with pheochromocytoma, and can backfire with insulinoma; a rare skin rash (necrolytic migratory erythema) is reported with prolonged use. R3
Rating
| Human Human evidence | Strong: approved for decades; RCTs and meta-analysis of newer forms R5 |
| Animal Animal / lab evidence | Not reviewed |
| Regulatory | FDA-approved R1 · not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R9, R10, R11 · not named by WADA R12 |
| Established human dose | Yes, label dose (see Study details) |
Evidence verdict: Severe low blood sugar: Strong (decades of use; RCTs of new forms) · Diagnostic aid for GI imaging: Strong (approved use) · Weight loss as glucagon alone: No human data
This page reports what studies used. It is not dosing advice.
Legend: HUMAN data · ANIMAL / LAB data · UNKNOWN · UNVERIFIED: not yet confirmed against a primary source
About the evidence: the core rescue effect is long established; newer formulation trials are often small and in controlled settings.
What is it?
Related pages: dasiglucagon, survodutide, mazdutide, retatrutide, pemvidutide.
Does it work?
- Human Rescue: nasal and injected glucagon were similarly effective in a meta-analysis of 8 RCTs. R5
- 🟨 Children: in a phase 1 study of 48 youth with type 1 diabetes, nasal glucagon raised blood sugar about as well as injected glucagon. R13
- Human Glucagon-receptor co-agonists (different drugs): retatrutide −24.2% body weight at 48 weeks (top dose) R6; survodutide −13.0% vs −5.4% at 76 weeks R7; mazdutide also tested in GLORY-1. R8
- ⚪ Glucagon alone for weight loss: no human data.
Is it safe?
- Contraindicated in pheochromocytoma; warnings for insulinoma, serious allergic reactions, poor effect when liver glycogen is low, and necrolytic migratory erythema. R3
- Nausea, vomiting and headache are among the most common reactions. R3, R4
Gray-market vials: extra risks
A gray-market vial has no quality control and no guarantee of identity, strength or sterility. We test retail vials blind under the Open Peptide Standard; see /tests/. A passing test covers one batch on one date and does not mean the compound is safe.
Is it legal?
- US: FDA-approved, prescription (Gvoke, Baqsimi, Fresenius Kabi glucagon and generics). R1, R2, R14 openFDA lists GlucaGen and Lilly's glucagon as discontinued. R15, R16
- Compounding: not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page. R9, R10, R11
- Sport: not named on WADA's 2026 Prohibited List. R12
Study details
Study details
These are amounts researchers used, not recommendations.
| Study | People / model | Route | Amount used | Follow-up | Reported | Citation |
|---|---|---|---|---|---|---|
| Sherr 2016 (phase 1) | 48 youth with T1D | Nasal vs IM | Per study | Single doses | 58 of 59 nasal doses raised glucose ≥25 mg/dL within 20 min | PMID 26884472 |
| Pontiroli 2020 meta-analysis | 8 RCTs, T1D | Nasal vs injected | Per study | Single doses | Similar efficacy | PMID 32025860 |
| Gvoke label | Adults and children 2+ | SC | Per label | Rescue use | Approved for severe hypoglycemia | R3 |
Full reference list (PubMed, CT.gov, FDA and WADA checked Oct 27, 2026)
- R1 Drugs@FDA, Gvoke (glucagon), application NDA212097 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA212097
- R2 Drugs@FDA, Baqsimi (glucagon nasal powder), application NDA210134 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA210134
- R3 Gvoke prescribing information, label published Jul 7, 2026 (DailyMed, checked Oct 27, 2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=359982a8-ec5c-4927-8c0f-89771e0f942b
- R4 Baqsimi prescribing information, label published Jun 19, 2026 (DailyMed, checked Oct 27, 2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=32ba41fa-4158-40af-8cb2-03693c248994
- R5 Pontiroli AE, et al. Acta Diabetol. 2020. PMID 32025860
- R6 Jastreboff AM, et al. N Engl J Med. 2023. PMID 37366315
- R7 le Roux CW, et al. N Engl J Med. 2026. PMID 42253238
- R8 Ji L, et al. N Engl J Med. 2025. PMID 40421736
- R9 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
- R10 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
- R11 FDA, Certain bulk drug substances for use in compounding that may present significant safety risks (content current Apr 22, 2026). https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks
- R12 WADA. The 2026 Prohibited List, full list checked; compound not named. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf
- R13 Sherr JL, et al. Diabetes Care. 2016. PMID 26884472
- R14 Drugs@FDA, Glucagon (Fresenius Kabi), application NDA201849 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA201849
- R15 Drugs@FDA, GlucaGen (glucagon), application NDA020918 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA020918
- R16 Drugs@FDA, Glucagon (Lilly), application NDA012122 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA012122
Disclaimer
This page is for education and harm reduction, not medical advice or a recommendation to use Glucagon (Gvoke, Baqsimi, generics). This is a prescription medicine. Use it only under the care of a licensed clinician; do not buy it from research-chemical or gray-market sellers. Report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).