Product image of Glucagen (Glucagon) supplied by GNH India

Glucagen

Active Ingredient:
Glucagon
Origin:
EU

Glucagen (Glucagon)

Glucagen is a prescription injectable solution containing 1 mg/mL of the peptide hormone glucagon. Marketed in the European Union, this medication is supplied as a sterile liquid for intramuscular, intravenous, or subcutaneous administration. Glucagon acts as an antihypoglycemic agent by rapidly raising blood glucose levels, making Glucagen a standard emergency treatment for severe hypoglycemia and certain drug overdoses. It is available by prescription and is not classified as a controlled substance.

Manufacturer / TM Owner

Novo Nordisk A/S

1
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Indications & Clinical Uses

Glucagen is indicated for acute medical situations that require rapid elevation of blood glucose, particularly when oral carbohydrate administration is impractical or ineffective.

  • Severe hypoglycemia in patients with diabetes when oral glucose cannot be given or is ineffective.
  • Emergency treatment of insulin overdose to quickly restore normal glucose levels.
  • Management of beta‑blocker or calcium‑channel blocker overdose where hypoglycemia may be precipitated.
  • Pre‑hospital care of unconscious or non‑responsive patients with documented low blood sugar.
  • Situations requiring rapid glucose increase during surgical or procedural sedation.

Side Effects

The safety profile of Glucagen reflects its mechanism of rapidly increasing blood glucose; most adverse events are mild and transient.

Common

  • Nausea or vomiting
  • Abdominal discomfort or pain
  • Flushing or warmth sensation
  • Headache
  • Injection‑site pain, redness, or swelling
  • Transient dizziness

Serious

  • Allergic reactions such as anaphylaxis, urticaria, or angioedema
  • Marked hyperglycemia leading to osmotic diuresis
  • Cardiovascular effects including tachycardia, hypertension, or arrhythmias
  • Rare seizures or neurologic changes
  • Severe hypotension in susceptible individuals

Precautions & Warnings

Glucagen should be used with awareness of specific clinical considerations to minimize risk.

  • Verify hypoglycemia with a blood glucose measurement before administration when possible.
  • Use caution in patients with known glucagon allergy or previous severe reactions.
  • Monitor cardiac status in patients with underlying heart disease, as rapid glucose shifts can affect heart rate and blood pressure.
  • Adjust dose or avoid use in patients with pheochromocytoma or adrenal medullary tumors.
  • Pregnant or breastfeeding individuals should receive Glucagen only if the benefit outweighs potential risk, as safety data are limited.
  • Store the product according to label instructions; avoid freezing and protect from light.

Avoid Interactions

Glucagen may interact with other medications that affect glucose metabolism or cardiovascular function.

Avoid

  • Concurrent use of high‑dose insulin or insulin secretagogues without close glucose monitoring.
  • Beta‑blockers or calcium‑channel blockers in overdose situations where glucagon may mask symptoms.

Use with caution

  • Oral hypoglycemic agents (e.g., sulfonylureas, meglitinides) that could cause rebound hypoglycemia.
  • Medications that prolong QT interval, as rapid glucose changes may exacerbate arrhythmias.
  • Drugs that affect hepatic glycogen stores, such as corticosteroids, which may alter glucagon effectiveness.
  • Anticholinergic agents that could blunt the typical side‑effects of glucagon.

Frequently Asked Questions

Glucagen can be administered intramuscularly, intravenously, or subcutaneously; the choice depends on the clinical setting and availability of equipment.

Blood glucose typically begins to rise within 5 to 10 minutes after Glucagen injection, with a peak effect around 15 to 30 minutes.

Yes, Glucagen is approved for use in pediatric patients when severe hypoglycemia requires rapid glucose elevation, following appropriate dosing guidelines.

If glucose does not improve, a second dose may be administered after reassessing blood glucose and clinical status, according to local protocols.

Glucagen is often used in beta‑blocker overdose because it can counteract the drug’s effects on glucose metabolism, but monitoring for cardiovascular changes is essential.

Glucagen should be stored at controlled room temperature, protected from light, and should not be frozen; once reconstituted, it must be used promptly.

Allergic reactions, including anaphylaxis, are rare but possible; signs such as rash, swelling, or difficulty breathing require immediate medical attention.

Glucagon can cause transient increases in heart rate and blood pressure; patients with cardiovascular disease should be monitored closely.

No, Glucagen is a prescription‑only medication in the EU and must be prescribed by a qualified healthcare professional.

Intravenous administration is an approved route; however, if unintended, monitor the patient for rapid glucose changes and cardiovascular effects.

Glucagen may be used during pregnancy only when the potential benefit justifies the potential risk, as safety data are limited.

Glucagon stimulates hepatic glycogenolysis and gluconeogenesis, leading to the release of glucose into the bloodstream.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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