Glucagon Injection / Solution
Glucagon injection is an emergency treatment for severe low blood sugar (hypoglycemia) in people with diabetes, available as Gvoke HypoPen, Gvoke Kit, and Gvoke PFS for subcutaneous use.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
How we combine label and product data →
Gvoke is a ready-to-use form of glucagon, the hormone that tells the liver to release its stored sugar, kept on hand as an emergency rescue for people with diabetes whose blood sugar drops so low they cannot eat or drink to fix it. It has been on the U.S. market since about 2019 and, unlike older glucagon kits, needs no mixing. Most people tolerate it reasonably well, though nausea, vomiting and headache are common as they come around. Call 911 right after giving it, even if the person wakes up, and once they can swallow safely, give fast-acting carbohydrates so the low does not return.
Clinical pearls
- Show family, coworkers or teachers where it is kept and how to use it, since the person having the low cannot inject it.
- If there is no response in 15 minutes, a second dose from a new device can be given while help is coming.
- Vomiting is common on waking, so turn an unresponsive person onto their side until they are alert.
- It may not work well after starvation, adrenal insufficiency or repeated lows, because the liver needs stored sugar to release.
Patient information guide — a plain-language walkthrough of Glucagon Injection / Solution, written from its FDA label.
What Glucagon Injection / Solution is used for
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Glucagon injection (as Gvoke HypoPen, Gvoke Kit, and Gvoke PFS) is an emergency medicine for severe low blood sugar. Here is the full set of supported uses:
- Gvoke HypoPen, Gvoke Kit, and Gvoke PFS (subcutaneous injection): treatment of severe hypoglycemia in adults and children aged 2 years and older with diabetes
How Glucagon Injection / Solution works
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Glucagon is a naturally occurring hormone that works on the liver. When injected, it activates receptors on liver cells, telling them to break down stored glycogen (a form of stored sugar) and release glucose into the bloodstream — raising blood sugar back to a safe level. It also relaxes smooth muscle in parts of the stomach and intestines. For glucagon to raise blood sugar effectively, the liver must have enough stored glycogen. If glycogen stores are depleted — due to starvation, adrenal insufficiency, or prolonged low blood sugar — the drug may not work as expected.
Glucagon Injection / Solution dosage
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Gvoke HypoPen, Gvoke Kit, and Gvoke PFS are each given as a single subcutaneous injection into the lower abdomen, outer thigh, or outer upper arm — use whichever site is most accessible in an emergency. Each device contains one dose; do not reuse it. After injecting, call for emergency assistance immediately. If there is no response after 15 minutes, a second dose from a new device may be given while waiting for help to arrive.
- Inject as soon as severe hypoglycemia is recognized — do not delay
- Once the person responds, give oral carbohydrates (like juice or crackers) to help restore the liver's glycogen stores and prevent the low blood sugar from coming back
- Always read the Instructions for Use that came with your prescription before an emergency happens — so you and caregivers are prepared
Dosing details from the FDA-approved label
From the Glucagon Injection / Solution prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Severe hypoglycemia in adult and pediatric patients aged 12 years and older with diabetes (GVOKE, subcutaneous)
- 1 mg administered by subcutaneous injection into lower abdomen, outer thigh, or outer upper arm
- If there has been no response after 15 minutes, an additional 1 mg dose from a new GVOKE HypoPen, GVOKE PFS, or GVOKE Kit may be administered while waiting for emergency assistance
- Age 12 years and older
- Severe hypoglycemia in pediatric patients aged 2 to less than 12 years who weigh less than 45 kg (GVOKE, subcutaneous)
- 0.5 mg administered by subcutaneous injection into the lower abdomen, outer thigh, or outer upper arm
- If there has been no response after 15 minutes, an additional 0.5 mg dose from a new GVOKE HypoPen, GVOKE PFS, or GVOKE Kit may be administered while waiting for emergency assistance
- Weight less than 45 kg
- Severe hypoglycemia in pediatric patients aged 2 to less than 12 years who weigh 45 kg or greater (GVOKE, subcutaneous)
- 1 mg administered by subcutaneous injection into the lower abdomen, outer thigh, or outer upper arm
- If there has been no response after 15 minutes, an additional 1 mg dose from a new GVOKE HypoPen, GVOKE PFS, or GVOKE Kit may be administered while waiting for emergency assistance
- Weight 45 kg or greater
- Diagnostic aid in adults: relaxation of the stomach, duodenal bulb, duodenum, and small bowel (GVOKE VialDx, intravenous)
- 0.2 mg to 0.5 mg intravenously, after dilution with 0.9% Sodium Chloride Injection, injected via a 1-minute slow push
- Only for intravenous use under medical supervision; diluted solution may be stored for up to 8 hours
- Diagnostic aid in adults: relaxation of the colon (GVOKE VialDx, intravenous)
- 0.5 mg to 0.75 mg intravenously, after dilution with 0.9% Sodium Chloride Injection, injected via a 1-minute slow push
- Only for intravenous use under medical supervision; diluted solution may be stored for up to 8 hours
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Dosage and Administration of GVOKE for Subcutaneous Use to Treat Severe Hypoglycemia in Adult and Pediatric Patients Aged 2 Years and Older with Diabetes ( 2.1 ) • Important Administration Instructions • Administer GVOKE HypoPen, GVOKE PFS, or GVOKE Kit subcutaneously. These three presentations are referred to as GVOKE in this labeling • Administer GVOKE according to the printed instructions on the foil pouch label, carton, or the Instructions for Use. • Visually inspect GVOKE prior to administration. The solution should appear clear and colorless to pale yellow. • Administer GVOKE subcutaneously in the lower abdomen, outer thigh, or outer upper arm. • Call for emergency assistance immediately after administering the dose. • If there has been no response after 15 minutes, may administer an additional dose from a new HypoPen, GVOKE PFS, or GVOKE Kit while waiting for emergency assistance. • When the patient has responded to GVOKE, give oral carbohydrates. • Do not attempt to reuse GVOKE. Each GVOKE device or vial contains a single dose of glucagon. Do not reuse and discard any unused portion. • Recommended Dosage • Recommended dose for adult and pediatric patients aged 12 years of age and older is 1 mg. • Recommended dose for adult and pediatric patients aged 12 years of age and older is 1 mg. • The recommended dose for pediatric patients aged 2 to less than 12 years of age who weigh: o Less than 45 kg, is 0.5 mg o 45 kg or greater, is 1 mg Dosage and Administration of GVOKE VialDx for Intravenous Use as a Diagnostic Aid in Adults ( 2.2 ) • GVOKE VialDx is only for intravenous use under medical supervision. • The recommended diagnostic dose for relaxation of the stomach, duodenal bulb, duodenum, and small bulb is 0.2 mg to 0.5 mg; the recommended dose to relax the colon is 0.5 mg to 0.75 mg. • See the Full Prescribing Information for administration instructions for GVOKE VialDx. 2.1 Dosage and Administration of GVOKE for Subcutaneous Use to Treat Severe Hypoglycemia in Adult and Pediatric Patients Aged 2 Years and Older with Diabetes Important Administration Instructions To treat severe hypoglycemia in adult and pediatric patients aged 2 years and older with diabetes, administer GVOKE HypoPen, GVOKE PFS, or GVOKE Kit subcutaneously.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Glucagon Injection / Solution side effects
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Common side effects
- Nausea
- Vomiting
- Headache
- Injection site swelling or discomfort
- Abdominal pain (in children)
- Low blood sugar after the dose (hypoglycemia, especially in children)
- High blood sugar after the dose (hyperglycemia, especially in children)
- Hives (urticaria, in children)
When to get medical help
- Call 911 immediately after giving the injection — this is always required, even if the person wakes up
- Get emergency help if there is no response within 15 minutes after the injection
- Seek emergency care for signs of a severe allergic reaction: rash, trouble breathing, or a sudden drop in blood pressure
- Call a doctor if you notice unusual bruising or bleeding (especially if taking warfarin)
- Tell your doctor right away if blood pressure spikes significantly after the injection
- Get emergency care if the person develops low blood sugar symptoms again after initially recovering
The most common side effects reported in clinical studies include:
- Nausea and vomiting (very common in both adults and children)
- Headache
- Injection site swelling, discomfort, or reaction
- Abdominal pain (in children)
- Low blood sugar after the dose — hypoglycemia (especially in children)
- High blood sugar after the dose — hyperglycemia (especially in children)
- Hives (urticaria) in some children
Serious reactions are less common but require immediate attention: a severe allergic reaction (rash, trouble breathing, very low blood pressure) or a significant spike in blood pressure or heart rate should be treated as a medical emergency.
Glucagon Injection / Solution warnings and precautions
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- Pheochromocytoma: Do not use glucagon if you have this adrenal tumor — it can cause a dangerous, rapid rise in blood pressure.
- Insulinoma: Do not use if you have an insulin-producing tumor — glucagon can paradoxically trigger severe low blood sugar.
- Serious allergic reactions: Anaphylaxis (a life-threatening allergic reaction with trouble breathing and very low blood pressure) has been reported. Seek emergency care immediately if this occurs.
- Liver glycogen stores: Glucagon won't work well if the liver has little stored glycogen — this can happen with starvation, adrenal insufficiency, or chronic low blood sugar. Emergency backup (intravenous glucose) may be needed.
- Necrolytic migratory erythema (NME): A skin rash has been reported with continuous glucagon infusions — Gvoke products are not approved for continuous infusion use.
- Beta-blockers: Taking a beta-blocker medicine can cause a temporary rise in blood pressure and heart rate when glucagon is given — this may need treatment in people with coronary artery disease.
Glucagon Injection / Solution interactions
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A few medications can change how glucagon works or increase side effects — tell your prescriber about everything you take:
- Beta-blockers (e.g., metoprolol, atenolol): may cause a temporary spike in pulse and blood pressure after glucagon — may need treatment in people with heart disease
- Indomethacin (an anti-inflammatory pain reliever): may blunt glucagon's ability to raise blood sugar, or may even cause low blood sugar — blood glucose should be monitored
- Warfarin (a blood thinner): glucagon can increase warfarin's blood-thinning effect — watch for unusual bruising or bleeding, and warfarin dose adjustments may be needed
- Insulin: insulin works against glucagon — blood glucose should be monitored when both are involved in care
Interactions listed in the FDA-approved label
From the Glucagon Injection / Solution prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Beta-blockers: Patients taking beta-blockers may have a transient increase in pulse and blood pressure when given GVOKE or GVOKE VialDx. The increase in blood pressure and heart rate may require therapy in patients with coronary artery disease.
- Insulin: Insulin acts antagonistically to glucagon. Monitor blood glucose when GVOKE VialDx is used as a diagnostic aid in patients receiving insulin.
- Indomethacin: In patients taking indomethacin, GVOKE may lose its ability to raise blood glucose or may even produce hypoglycemia. Monitor blood glucose levels during glucagon treatment of patients taking indomethacin.
- Anticholinergic drugs: Concomitant use with GVOKE VialDx increases the risk of gastrointestinal adverse reactions due to additive effects on inhibition of gastrointestinal motility. Concomitant use of anticholinergic drugs with GVOKE VialDx is not recommended.
- Warfarin: GVOKE and GVOKE VialDx may increase the anticoagulant effect of warfarin. Monitor patients for unusual bruising or bleeding, as adjustments in warfarin dosage may be required.
Read the label’s full interactions text
7 DRUG INTERACTIONS Table 4: Clinically Significant Drug Interaction with GVOKE and GVOKE VialDx Beta-Blockers Clincial Impact: Patients taking beta-blockers may have a transient increase in pulse and blood pressure when given GVOKE or GVOKE VialDx. Intervention The increase in blood pressure and heart rate may require therapy in patients with coronary artery disease. Insulin Clincial Impact: Insulin acts antagonistically to glucagon. Intervention Monitor blood glucose when GVOKE VialDx is used as a diagnostic aid in patients receiving insulin. Indomethacin Clincial Impact: In patients taking indomethacin, GVOKE may lose its ability to raise blood glucose or may even produce hypoglycemia. Intervention Monitor blood glucose levels during glucagon treatment of patients taking indomethacin. Anticholinergic Drugs Clincial Impact: The concomitant use of anticholinergic drugs and GVOKE VialDx increases the risk of gastrointestinal adverse reactions due to additive effects on inhibition of gastrointestinal motility. Intervention Concomitant use of anticholinergic drugs with GVOKE VialDx is not recommended. Warfarin Clincial Impact: GVOKE and GVOKE Vial Dx may increase the anticoagulant effect of warfarin. Intervention Monitor patients for unusual bruising or bleeding, as adjustments in warfarin dosage may be required. Beta-blockers: GVOKE- or GVOKE VialDx-treated patients taking concomitant beta-blockers may have a transient increase in pulse and blood pressure. ( 7 ) Indomethacin: In patients taking concomitant indomethacin, GVOKE may lose its ability to raise glucose or may produce hypoglycemia. ( 7 ) Anticholinergic drugs: Concomitant use of anticholinergic drugs with GVOKE VialDx for use as a diagnostic aid is not recommended. ( 7 ) Warfarin: GVOKE and GVOKE VialDx may increase the anticoagulant effect of warfarin. ( 7 ) Insulin: Monitor blood glucose when GVOKE VialDx is used as a diagnostic aid in patients receiving insulin.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Glucagon Injection / Solution
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- Do not use if you have a pheochromocytoma (an adrenal tumor) — risk of dangerous blood pressure surge
- Do not use if you have an insulinoma (an insulin-producing pancreatic tumor) — risk of severe low blood sugar
- Do not use if you have had a previous serious allergic reaction to glucagon or any ingredient in Gvoke
- Tell your prescriber if you are pregnant — available evidence has not shown harm to the baby, but data are limited
- Breastfeeding is likely safe — glucagon is a protein expected to break down in the infant's gut and is unlikely to cause harm; discuss with your doctor
- Not approved for children under 2 years of age
- May be less effective if you are malnourished, have adrenal insufficiency, or have had prolonged or repeated episodes of low blood sugar — the liver may lack sufficient glycogen stores
- Older adults: clinical studies did not include enough patients over 65 to know if they respond differently; use with the same caution and follow your prescriber's guidance
Glucagon Injection / Solution overdose
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Too much glucagon can cause nausea, vomiting, a slowdown of the digestive tract, and a rise in blood pressure and heart rate. Blood potassium levels may drop and should be monitored and corrected if needed. If you suspect an overdose, contact the Poison Help line at 1-800-222-1222 or seek emergency medical care right away.
What Glucagon Injection / Solution does in the body
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After a subcutaneous injection, glucagon raises blood glucose by triggering the liver to release stored sugar. In adults with type 1 diabetes, blood sugar levels rise significantly within a short window after injection. In children with type 1 diabetes (ages 2 to under 18), meaningful rises in blood glucose are also seen, with the size of the increase varying somewhat by age group. Glucagon also relaxes smooth muscle in the stomach, small intestine, and colon — an effect that has separate uses in medical imaging procedures.
How your body processes Glucagon Injection / Solution
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After a subcutaneous injection in adults, glucagon is absorbed relatively quickly, reaching peak levels in the bloodstream in about 50 minutes. Its half-life — the time it takes for the body to clear half the drug — is about 32 minutes. Glucagon is broken down extensively by the liver, kidneys, and blood plasma. In children, age-appropriate doses produce similar glucagon blood levels across age groups, with peak levels reached somewhat earlier in younger children.
How to store Glucagon Injection / Solution
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Store GVOKE HypoPen, GVOKE PFS, and GVOKE Kit (these three presentations are referred to as GVOKE in this labeling), and GVOKE VialDx at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F). Do not refrigerate or freeze.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Glucagon Injection / Solution: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Glucagon Injection / Solution — the kind of thing our pharmacy team would talk through with you at the counter.
When exactly should I use Gvoke — and is it really an emergency?
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What do I do after I give the injection?
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What side effects should I expect after using Gvoke?
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What if I take a blood thinner like warfarin or a beta-blocker — is Gvoke still safe to use?
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Will Gvoke work for everyone with diabetes who has a severe low?
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Is it safe to use Gvoke during pregnancy or while breastfeeding?
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Is Glucagon Injection / Solution available over the counter?
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When was Glucagon Injection / Solution first available?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Glucagon Injection / Solution on HelloPharmacist
Glucagon Injection / Solution forms and strengths (how it comes)
Glucagon Injection / Solution is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Injection
How this form is used
- Gvoke HypoPen, Gvoke Kit, and Gvoke PFS are each approved to treat severe hypoglycemia (dangerously low blood sugar) in adults and children aged 2 years and older with diabetes
- Gvoke HypoPen, Gvoke Kit, and Gvoke PFS are administered subcutaneously (under the skin) — not intravenously
- Gvoke HypoPen and Gvoke PFS: do not open the foil pouch until you are ready to inject
- Gvoke Kit: keep in the original carton until ready to use
- Gvoke HypoPen, Gvoke PFS, and Gvoke Kit: inject subcutaneously into the lower abdomen, outer thigh, or outer upper arm — then call for emergency help immediately
- Gvoke HypoPen, Gvoke PFS, and Gvoke Kit each contain a single dose — do not reuse; discard any unused portion
Glucagon Injection / Solution on the U.S. market: products, makers and brands
How Glucagon Injection / Solution appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
1 company lists 19 Glucagon Injection / Solution product records with the FDA, mostly as injection; the earliest marketing or approval year on record is 2019. Brand names on the directory include Gvoke Kit, Gvoke HypoPen, Gvoke PFS and 3 more; the rest are generics.
How widely Glucagon Injection / Solution is used (Medicaid data)
A general measure of how commonly Glucagon Injection / Solution is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q2 2025 – Q1 2026, summed across every form and brand of the drug.
Think of this as a proxy for how widely Glucagon Injection / Solution is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Glucagon Injection / Solution prescribed? Of the 1,599 medications we measure, Glucagon Injection / Solution ranks #577 by Medicaid prescriptions — more than 64% of them.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Glucagon Injection / Solution, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 6 of 12 listed Glucagon Injection / Solution NDCs with Medicaid activity.
Compare Glucagon Injection / Solution products
A representative set of FDA-listed product records for Glucagon Injection / Solution — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Injection | ||||
| 0.5 mg/0.1 mL | Subcutaneous | Xeris Pharmaceuticals, Inc. × 5 listings | NDA | View NDC → |
| 1 mg/0.2 mL | Subcutaneous | Xeris Pharmaceuticals, Inc. × 14 listings | NDA | View NDC → |
Showing 19 of 19 products — FDA National Drug Code Directory. See every product, package size and price: browse all 19 Glucagon Injection / Solution NDCs →
Glucagon Injection / Solution side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Glucagon Injection / Solution — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Glucagon Injection / Solution in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Glucagon Injection / Solution FDA approval history
How Glucagon Injection / Solution went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Glucagon Injection / Solution recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Glucagon Injection / recalls since July 2021.
✅No Glucagon Injection / recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
Glucagon Injection / Solution supply and shortage status
Whether Glucagon Injection / Solution is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
Glucagon Injection / Solution brand names
Glucagon Injection / Solution is sold under 6 brand names in the FDA directory — Gvoke Kit, Gvoke HypoPen, Gvoke PFS, Gvoke PFS 1 mg Pre-filled Syringe and others. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Glucagon Injection / Solution: manufacturers and labelers
One company lists Glucagon Injection / Solution products with the FDA. By number of product records, the largest are Xeris Pharmaceuticals, Inc.. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Sources for this Glucagon Injection / Solution page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Xeris Pharmaceuticals, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →