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FDA approved Glucagon for Injection as Diagnostic Aid During Radiologic ExaminationsFDA approved Glucagon to Help Keep the Gut Still During Imaging

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Key Takeaway
Note: Glucagon for Injection is not for emergency hypoglycemia; use only as a diagnostic aid during radiologic exams.

The FDA has approved Glucagon for Injection for use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal tract. This approval provides clinicians with a pharmaceutical option to reduce GI motility during imaging procedures, potentially improving diagnostic accuracy.

The approval specifies that Glucagon for Injection is not indicated for the emergency treatment of hypoglycemia, as it is not packaged with a syringe and diluent necessary for rapid preparation and administration outside of a healthcare facility. This distinction is critical for emergency settings.

Dosing depends on the diagnostic procedure, route of administration, and expected procedure duration. For inhibition of stomach and small bowel motility, the recommended dose is 0.2 mg to 0.5 mg intravenously or 1 mg intramuscularly. For colon motility, the dose is 0.5 mg to 0.75 mg intravenously or 1 mg to 2 mg intramuscularly. Bolus doses above 1 mg intravenously have caused nausea and vomiting and are not recommended.

Clinical Details (Mechanism · Dosing · Trial Data · Warnings)
Mechanism of Action

Glucagon for Injection is a gastrointestinal motility inhibitor. Its mechanism of action is not described in the label.

Indication & Patient Population

Glucagon for Injection is indicated for use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal tract. It is not indicated for the emergency treatment of hypoglycemia because it is not packaged with a syringe and diluent necessary for rapid preparation and administration during an emergency outside of a healthcare facility. The patient population is not further specified in the label.

Dosing & Administration

Reconstitute lyophilized powder with Sterile Water for Injection before use. Determine dose based on diagnostic procedure, route of administration, and procedure duration. To inhibit stomach and small bowel motility, the dose is 0.2 mg to 0.5 mg given intravenously or 1 mg given intramuscularly. To inhibit colon motility, the dose is 0.5 mg to 0.75 mg given intravenously or 1 mg to 2 mg given intramuscularly. Bolus doses above 1 mg administered intravenously have caused nausea and vomiting and are not recommended. Reconstitute by injecting 1 mL of Sterile Water for Injection into the vial, shake gently until dissolved, and inspect for particulate matter and discoloration. The reconstituted solution has a concentration of approximately 1 mg per mL and should be used immediately. Administer by medical personnel. If given intravenously, administer as a bolus over 1 minute. Discard any unused portion. After the procedure, give oral carbohydrates to patients who have been fasting, if compatible with the diagnostic procedure.

Key Clinical Trial Data

Trial data not available in label.

Warnings & Contraindications

Glucagon for Injection is contraindicated in patients with pheochromocytoma because of the risk of increased blood pressure, and in patients with insulinoma or glucagonoma because of the risk of hypoglycemia. Drug interactions include beta-blockers; the clinical impact is described in the label but not fully detailed here.

Place in Therapy

Glucagon for Injection is approved as a diagnostic aid for radiologic examinations to temporarily inhibit GI motility. It is not for emergency hypoglycemia treatment. Its place in therapy is as a procedural adjunct, with dosing tailored to the specific examination and route.

The FDA has approved a new use for Glucagon for Injection. This medicine is given during certain radiologic exams to temporarily slow down movement in the stomach, small bowel, and colon. When the gut stays still, images can be clearer, which may help doctors make a more accurate diagnosis.

This approval is for people who are having these imaging procedures. It is not for the emergency treatment of very low blood sugar. The version approved here does not come with a syringe and diluent needed for fast preparation outside a healthcare facility. That difference matters for emergency settings.

The dose depends on the procedure, how it is given, and how long the exam is expected to last. For stomach and small bowel, the dose is 0.2 mg to 0.5 mg intravenously or 1 mg intramuscularly. For colon, it is 0.5 mg to 0.75 mg intravenously or 1 mg to 2 mg intramuscularly. Doses above 1 mg intravenously have caused nausea and vomiting and are not recommended.

If you have an imaging exam coming up, talk with your doctor about whether this medicine is right for you. This approval does not change emergency care for low blood sugar.

What this means for you:
This approval helps imaging exams, not emergency low blood sugar.

Study Details

Study typeFda approval
PublishedMay 2015
View Original Abstract ↓
1 INDICATIONS AND USAGE Glucagon for Injection is indicated for use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal tract. Limitations of Use : Glucagon for Injection is not indicated for the emergency treatment of hypoglycemia because it is not packaged with a syringe and diluent necessary for rapid preparation and administration during an emergency outside of a healthcare facility. Glucagon for Injection is a gastrointestinal motility inhibitor indicated for use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal (GI) tract ( 1 ) Limitations of Use: Glucagon for Injection is not indicated for the emergency treatment of hypoglycemia ( 1 )
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