Product image of Glucagen (Glucagon) supplied by GNH India

Glucagen

Active Ingredient:
Glucagon
Origin:
EU

Glucagen (Glucagon)

Glucagen is an injectable solution containing the hormone glucagon. It is supplied in a dosage form for intramuscular or subcutaneous administration, with strength not specified in the EU market. As a prescription‑only product, Glucagen is used by healthcare professionals to rapidly increase blood glucose levels in emergency situations. The medication is stored in a sealed vial and must be reconstituted immediately before use according to the manufacturer's instructions.

Manufacturer / TM Owner

Novo Nordisk A/S

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Indications & Clinical Uses

Glucagen is indicated for acute management of conditions that require a rapid rise in blood glucose.

  • Treatment of severe hypoglycemia in patients with diabetes when oral glucose is ineffective or unavailable.
  • Emergency reversal of insulin‑induced hypoglycemia in unconscious or non‑responsive individuals.
  • Off‑label use for suspected beta‑blocker overdose to counteract prolonged hypoglycemia.
  • Supportive therapy in cases of prolonged fasting or glycogen storage disease where glucose cannot be maintained.
  • Use in diagnostic testing for adrenal insufficiency when a glucagon stimulation test is required.

Side Effects

Glucagen may cause a range of physiological responses after injection, varying from mild to severe.

Common

  • Nausea or vomiting.
  • Flushing or warmth sensation.
  • Headache.
  • Transient rise in blood pressure.
  • Local injection site pain or erythema.

Serious

  • Severe allergic reaction (anaphylaxis) with difficulty breathing or swelling.
  • Persistent hyperglycemia requiring medical intervention.
  • Cardiac arrhythmias in patients with underlying heart disease.

Precautions & Warnings

When prescribing or administering Glucagen, clinicians should consider several safety factors to minimize risk.

  • Verify the patient’s diagnosis of hypoglycemia and rule out contraindications such as pheochromocytoma.
  • Use caution in patients with known hypersensitivity to glucagon or any excipients.
  • Monitor blood glucose closely after administration to avoid overshoot hyperglycemia.
  • Adjust dose in pediatric patients according to weight and clinical response.
  • Avoid use in patients with severe cardiovascular disease without specialist consultation.
  • Ensure proper reconstitution and avoid contamination of the vial.

Avoid Interactions

Glucagen can interact with other medications, influencing its effectiveness or safety profile.

Avoid

  • Concurrent use of beta‑adrenergic antagonists that may blunt the glucose‑raising effect.
  • Co‑administration with insulin analogs in excess, which can precipitate recurrent hypoglycemia.

Use with caution

  • Oral hypoglycemic agents (e.g., sulfonylureas) that may require dose adjustment after glucagon administration.
  • Medications that affect cardiac conduction (e.g., quinidine) due to potential arrhythmia risk.
  • Steroids or catecholamines that may amplify hyperglycemic response.

Frequently Asked Questions

Glucagen is primarily used to rapidly raise blood glucose levels in patients experiencing severe hypoglycemia when oral glucose cannot be administered.

Glucagen is supplied as an injectable solution and can be given by intramuscular or subcutaneous injection.

Although not formally approved, Glucagen is sometimes used off‑label to counteract prolonged hypoglycemia associated with beta‑blocker overdose.

Common side effects include nausea, vomiting, flushing, headache, a temporary rise in blood pressure, and mild pain or redness at the injection site.

Serious reactions such as anaphylaxis, persistent hyperglycemia, or cardiac arrhythmias require urgent medical evaluation.

Glucagen should be avoided in patients with a documented hypersensitivity to glucagon or any of its excipients.

Concurrent use with high‑dose insulin may increase the risk of recurrent hypoglycemia; dosing should be coordinated by a healthcare professional.

Glucagen should be kept in a sealed vial, protected from light, and stored at the temperature recommended by the manufacturer, typically between 2 °C and 8 °C.

Blood glucose should be measured regularly after injection to ensure the desired rise and to detect possible hyperglycemia.

Glucagen may be used in pediatric patients, but dosing should be weight‑based and determined by a qualified clinician.

Do not use the product; a discolored or cloudy solution may indicate degradation or contamination and should be discarded.

No, Glucagen is classified as a prescription‑only medication (Rx) in the European Union.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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