Product image of Glucagen (Glucagon) supplied by GNH India

Glucagen

Active Ingredient:
Glucagon
Origin:
EU

Glucagen (Glucagon)

Glucagen is a prescription medication whose active ingredient is glucagon, a peptide hormone used to raise blood glucose levels. It is supplied in injectable form for intramuscular, intravenous, or subcutaneous administration, and is marketed in the European Union. The product is intended for emergency treatment of acute hypoglycemia in patients who are unable to ingest carbohydrates orally and should be administered by trained healthcare professionals.

Manufacturer / TM Owner

Novo Nordisk - Comércio De Produtos Farmacêuticos, Lda

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Indications & Clinical Uses

Glucagen is indicated for the rapid correction of severe hypoglycemia when oral glucose is not feasible.

  • Emergency treatment of acute hypoglycemia in diabetic patients.
  • Management of hypoglycemia in patients receiving insulin or sulfonylureas.
  • Use in cases of insulin overdose or accidental ingestion.
  • Treatment of hypoglycemia during anesthesia or surgery.
  • Support for patients with adrenal insufficiency experiencing low blood sugar.
  • Use as a diagnostic aid in evaluating pancreatic alpha‑cell function.
  • Administration in cases of severe malnutrition‑related hypoglycemia.
  • The medication is delivered as a ready‑to‑use solution that can be given quickly by injection.

Side Effects

Glucagen may cause a range of adverse reactions, most of which are transient and related to its pharmacologic action.

Common

  • Nausea or vomiting
  • Flushing or warmth sensation
  • Headache
  • Dizziness
  • Mild abdominal discomfort
  • Transient increase in blood pressure
  • Sweating
  • Feeling of anxiety
  • Tremor
  • Cold extremities
  • Mild chest discomfort
  • Transient visual disturbances
  • Mild fatigue

Serious

  • Severe allergic reaction (anaphylaxis)
  • Rapid heart rate (tachycardia) or palpitations
  • Low blood pressure (hypotension) leading to fainting
  • Seizures
  • Severe hypoglycemia rebound
  • Cardiac arrhythmias
  • Pulmonary edema
  • Stroke
  • Severe hyperglycemia
  • Renal impairment
  • Multi-organ failure
  • Severe metabolic acidosis
  • Transient visual disturbances
  • Stroke
  • Severe metabolic acidosis

Precautions & Warnings

When using Glucagen, healthcare providers should observe specific precautions to ensure safe and effective administration.

  • Verify hypoglycemia before administration; avoid use if blood glucose is >70 mg/dL.
  • Use only in emergency situations where oral carbohydrate intake is impossible.
  • Ensure correct reconstitution and dosage according to prescribing information.
  • Monitor patient vital signs after injection, especially heart rate and blood pressure.
  • Store the product according to temperature guidelines to maintain potency.
  • Educate patients and caregivers on proper injection technique and emergency use.

Avoid Interactions

Glucagen can interact with certain medications and clinical conditions; awareness of these interactions helps prevent adverse outcomes.

Avoid

  • Concurrent use with beta‑blockers that may mask tachycardia symptoms.
  • Administration together with other glucagon‑like agents that could cause excessive hyperglycemia.
  • Use in patients receiving high‑dose insulin infusions without appropriate monitoring.
  • Co‑administration with vasopressors may exacerbate peripheral vasoconstriction.
  • Concurrent use with oral contraceptives may alter glucagon metabolism.

Use with caution

  • Patients with cardiovascular disease; monitor for arrhythmias.
  • Individuals with pheochromocytoma; risk of hypertensive crisis.
  • Pregnant or lactating women; limited safety data, consider risk‑benefit.
  • Patients with renal impairment; dosage adjustment may be required.
  • Individuals with hepatic disease; reduced glycogen stores may affect response.

Frequently Asked Questions

Glucagen contains glucagon as its active ingredient, a hormone that raises blood glucose levels.

Glucagen is given by injection, either intramuscularly, intravenously, or subcutaneously, depending on the clinical situation.

Glucagen should not be used if the patient’s blood glucose is already above 70 mg/dL or if oral glucose can be taken safely.

Glucagen may be used in pediatric patients under medical supervision, following appropriate dosing guidelines.

Common side effects include nausea, vomiting, flushing, headache, dizziness, and mild abdominal discomfort.

Serious reactions such as anaphylaxis, severe allergic response, rapid heart rate, low blood pressure, seizures, or cardiac arrhythmias need urgent care.

Glucagen should be stored according to the manufacturer’s temperature recommendations, typically between 2 °C and 8 °C, to maintain potency.

Safety data for use during pregnancy are limited; the drug should be used only if the potential benefit justifies the potential risk.

Yes, beta‑blockers may mask the tachycardia that can occur after Glucagen administration, so caution is advised.

Patients should be monitored for vital signs, especially heart rate and blood pressure, and for any adverse reactions.

Glucagen is a prescription‑only medication in the European Union.

Patients with renal impairment may need dosage adjustments and close monitoring when receiving Glucagen.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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