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, supplied in an injectable form without a specified strength. It is marketed in the European Union and is classified as a peptide hormone. Glucagen is administered via intramuscular, intravenous, or subcutaneous routes to rapidly raise blood glucose levels in emergency situations. The drug is intended for use by healthcare professionals when a patient experiences severe hypoglycemia and requires glucose restoration.

Manufacturer / TM Owner

Novo Nordisk Pharma Gmbh

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Indications & Clinical Uses

Glucagen is indicated for the rapid treatment of severe hypoglycemia when oral glucose administration is not feasible or effective.

  • Emergency treatment of insulin‑induced hypoglycemia in adults and children.
  • Management of hypoglycemia caused by sulfonylurea overdose.
  • Use in patients with adrenal insufficiency who develop hypoglycemic episodes.
  • Administration during diagnostic procedures that may provoke low blood glucose, such as oral glucose tolerance tests.

Side Effects

The safety profile of Glucagen includes both common, generally mild reactions and rare, potentially serious events.

Common

  • Nausea or vomiting.
  • Flushing or warmth at the injection site.
  • Headache.
  • Transient rise in blood pressure.

Serious

  • Severe allergic reaction (anaphylaxis) with rash, itching, swelling, or difficulty breathing.
  • Cardiac arrhythmias or rapid heart rate.
  • Persistent hyperglycemia requiring medical attention.

Precautions & Warnings

Before using Glucagen, healthcare providers should consider several precautionary measures to ensure safe administration.

  • Verify the patient’s diagnosis of hypoglycemia and assess the need for injectable glucagon.
  • Use only with a new, sterile needle and syringe for each dose.
  • Avoid administration in patients with known hypersensitivity to glucagon or any excipients.
  • Monitor blood glucose levels after injection to confirm response.
  • Be cautious in patients with pheochromocytoma or severe cardiovascular disease.
  • Do not use in patients who are pregnant or breastfeeding unless the benefit outweighs the risk (category unknown).

Avoid Interactions

Glucagen may interact with other medications, influencing its effectiveness or increasing the risk of adverse effects.

Avoid

  • Concurrent use of beta‑blockers, which may mask typical glucagon‑induced tachycardia.
  • Combination with insulin secretagogues (e.g., sulfonylureas) that could precipitate recurrent hypoglycemia after glucagon wears off.

Use with caution

  • Patients receiving catecholamines or other vasopressors, as glucagon can augment cardiovascular effects.
  • Individuals on oral anticoagulants, because rapid glucose shifts may affect coagulation parameters.
  • Use in conjunction with other peptide hormones, monitoring for additive hemodynamic changes.

Frequently Asked Questions

Glucagen contains glucagon, which raises blood glucose by stimulating hepatic glycogenolysis and gluconeogenesis.

Glucagen is used when a patient has severe hypoglycemia and cannot take oral glucose, such as unconsciousness or seizures.

Yes, Glucagen can be administered intravenously, as well as intramuscularly or subcutaneously, depending on the clinical situation.

Glucagen is a prescription‑only medication (Rx) and requires a healthcare provider’s order.

Common side effects include nausea, vomiting, flushing, headache, and a temporary increase in blood pressure.

Signs of anaphylaxis, severe cardiac arrhythmias, or persistent high blood glucose should be evaluated promptly.

The pregnancy category for Glucagen is unknown; it should be used only if the potential benefit justifies the potential risk.

Glucagen should be kept in a refrigerator (2‑8 °C) and protected from light; do not freeze.

Beta‑blockers may mask the typical increase in heart rate after glucagon, so clinicians should monitor patients closely.

Yes, excessive dosing can cause transient hyperglycemia, which may require monitoring and treatment.

Glucagen is classified under ATC code H01BA01, which corresponds to glucagon.

Glucagen is indicated for severe hypoglycemia in both adults and children when administered by a qualified professional.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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