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What the label lists and what reports show

Glucagon side effects

Glucagon's FDA label lists its adverse reactions in its own words. FAERS holds 4,129 reports naming it through July 30, 2026; the reaction reported most often, leaving out the conditions it is used for, product-use terms and outcomes, is dyspnoea (367 reports).

  • Generic listed

Check it at the source: the glucagon FDA label on DailyMed (effective August 11, 2026, Amphastar Pharmaceuticals, Inc.); the FDA FAERS public dashboard.

What does the patient leaflet say about side effects?

From the patient leaflet: What are the possible side effects of Glucagon?

Glucagon may cause serious side effects, including: High blood pressure. Glucagon can cause high blood pressure in certain people with tumors in their adrenal glands. Low blood sugar. Glucagon can cause low blood sugar in patients with tumors in their pancreas called insulinomas and Glucagonomas by making too much insulin in their bodies. Serious allergic reactions. Call your doctor or get medical help right away if you have a serious allergic reaction including: rash difficulty breathing low blood pressure High blood sugar. If you receive Glucagon before your radiology exam it can cause high blood sugar. Your doctor will monitor your blood sugar levels during your treatment. Heart problems. […]

Source: FDA drug label (Glucagon), Fresenius Kabi USA, LLC, effective September 16, 2020 (SPL set e4be1c0e-0fe6-45a0-9229-5cde98434b84), via openFDA; the full label on DailyMed

What does the label list?

From the label: adverse reactions

The following important adverse reactions are described below and elsewhere in the labeling: Hypersensitivity and Allergic Reactions [see Warnings and Precautions (5.3)] Necrolytic Migratory Erythema [ see Warnings and Precautions (5.5) ] Hyperglycemia in Patients with Diabetes Mellitus when Used as a Diagnostic Aid [ see Warnings and Precautions (5.6) ] Blood Pressure and Heart Rate Increase in Patients with Cardiac Disease when used as a Diagnostic Aid [ see Warnings and Precautions (5.7) ] The following adverse reactions have been identified during post-approval use of glucagon. Because these reactions are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to drug exposure. …

Table 2: Adverse Reactions Occurring ≥5% in Healthy Subjects Who Received Glucagon for Injection Subcutaneously

This table is printed in the Glucagon label published by Fresenius Kabi USA, LLC of September 16, 2020; the label quoted above does not print one.

ReactionGlucagon for Injection (N=31) % of Patients
Injection site swelling58
Injection site erythema55
Vomiting36
Nausea32
Decreased blood pressure23
Asthenia23
Headache13
Dizziness10
Pallor10
Diarrhea7
Somnolence7

Rows and numbers as the label prints them, under its own column headings (the first rows of a longer table where it runs on). A reaction in a trial table is not necessarily caused by the medicine, and trials differ from everyday use.

Source: FDA drug label, Amphastar Pharmaceuticals, Inc., effective August 11, 2026 (SPL set 8cc40354-b5ac-45b6-a211-93b44444f2a3), via openFDA; the full label on DailyMed

What do FAERS reports show?

4,129 reports list glucagon among the medicines taken, each a report of something that happened, not proof the medicine caused it; 669 are coded as a death and 1,990 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Of the 19 reactions below, 4 are named by the same term (in US spelling) in the label's adverse reactions, warnings or patient leaflet; a reaction the label does not name may still be there under another word, and a report does not show that the medicine caused it.

Reports received each year

The 25 most reported reactions

  • Drug Ineffective (a use or a product term, not a reaction)381
  • Dyspnoea367
  • Acute Kidney Injury320
  • Hypotension (named in the label)293
  • Hypoglycaemia271
  • Condition Aggravated (a use or a product term, not a reaction)253
  • Toxicity To Various Agents238
  • Nausea (named in the label)232
  • Anxiety218
  • Haemoptysis218
  • Death (an outcome recorded in the report)214
  • Vomiting (named in the label)212
  • Pain In Extremity206
  • Off Label Use (a use or a product term, not a reaction)199
  • Blood Glucose Decreased198
  • Blood Glucose Increased198
  • Asthma195
  • Headache (named in the label)186
  • Pneumonia181
  • Intentional Overdose (a use or a product term, not a reaction)178
  • Lung Disorder178
  • Wheezing178
  • Pulmonary Fibrosis173
  • Renal Failure173
  • Therapeutic Product Effect Incomplete (a use or a product term, not a reaction)173

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026; reactions as MedDRA preferred terms

What next?

Glucagon: the full record
label, generics, price, shortages, recalls
Side effects hub
the most reported medicines and reactions