Drugplain

Gvoke HypoPen 0.5 mg Auto-Injector .5 mg/.1mL

glucagon injection, solution · INJECTION, SOLUTION · Xeris Pharmaceuticals, Inc.

No Recall History
Plain English

Gvoke HypoPen 0.5 mg Auto-Injector is a injection, solution containing glucagon injection, solution at .5 mg/.1mL, taken subcutaneous. Manufactured by Xeris Pharmaceuticals, Inc..

Key Facts

Brand Name
Gvoke HypoPen 0.5 mg Auto-Injector
Generic Name
glucagon injection, solution
NDC Code (Product)
72065-120
Manufacturer
Xeris Pharmaceuticals, Inc.
Strength
.5 mg/.1mL
Dosage Form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Marketing Status
Application #
NDA212097
Drug Class
Antihypoglycemic Agent [EPC]; Gastrointestinal Motility Inhibitor [EPC]
Marketing Start
09/10/2019

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

abdominal pain upper1 reports
aphasia1 reports
arthralgia1 reports
blood creatinine increased1 reports
blood glucose decreased1 reports
blood urea increased1 reports
chest discomfort1 reports
clumsiness1 reports
constipation1 reports
dizziness1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE • GVOKE is an antihypoglycemic agent indicated for subcutaneous use for the treatment of severe hypoglycemia in adult and pediatric patients aged two years and older with diabetes ( 1.1 ) • GVOKE VialDx is a gastrointestinal motility inhibitor indicated for intravenous use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal tract in adult patients ( 1.2 ) 1.1 Severe Hypoglycemia in Adult and Pediatric Patients Aged 2 Years and Older with Diabetes GVOKE is indicated for subcutaneous use for the treatment of severe hypoglycemia in adult and pediatric patients aged two and older with diabetes. 1.2 Diagnostic Aid in Adults GVOKE VialDx is indicated for intravenous use as a diagnostic aid during radiologic examinations to temporarily inhibit movement of the gastrointestinal tract in adult patients.

Dosage & Administration

2 DOSAGE AND ADMINISTRATION Dosage and Administration of GVOKE for Subcutaneous Use to Treat Severe Hypoglycemia in Adult and Pediatric Patients Aged 2 Years and Older with Diabetes ( 2.1 ) • Important Administration Instructions • Administer GVOKE HypoPen, GVOKE PFS, or GVOKE Kit subcutaneously. These three presentations are referred to as GVOKE in this labeling • Administer GVOKE according to the printed instructions on the foil pouch label, carton, or the Instructions for Use. • Visually inspect GVOKE prior to administration. The solution should appear clear and colorless to pale yellow. • Administer GVOKE subcutaneously in the lower abdomen, outer thigh, or outer upper arm. • Call for emergency assistance immediately after administering the dose. • If there has been no response after 15 minutes, may administer an additional dose from a new HypoPen, GVOKE PFS, or GVOKE Kit while waiting for emergency assistance. • When the patient has responded to GVOKE, give oral carbohydrates. • Do not attempt to reuse GVOKE. Each GVOKE device or vial contains a single dose of glucagon. Do not reuse and discard any unused portion. • Recommended Dosage • Recommended dose for adult and pediatric

Contraindications

4 CONTRAINDICATIONS GVOKE and GVOKE VialDx are contraindicated in patients with: • Pheochromocytoma because of the risk of substantial increase in blood pressure [see Warnings and Precautions ( 5.1 )] • Insulinoma because of the risk of hypoglycemia [see Warnings and Precautions ( 5.2 )] • Prior hypersensitivity reaction to glucagon or to any of the excipients in GVOKE or GVOKE VialDx. Serious hypersensitivity reactions have been reported with glucagon and include anaphylactic shock with breathing difficulties and hypotension [see Warnings and Precautions ( 5.3 )] . GVOKE VialDx for use as a diagnostic aid is also contraindicated in patients with glucagonoma because of risk of hypoglycemia [see Warnings and Precautions ( 5.8 )] • Pheochromocytoma ( 4 ) • Insulinoma ( 4 ) • Prior hypersensitivity reaction to glucagon or to any of the excipients ( 4 ) • Glucagonoma when used as a diagnostic aid ( 4 )

Drug Interactions

7 DRUG INTERACTIONS Table 4: Clinically Significant Drug Interaction with GVOKE and GVOKE VialDx Beta-Blockers Clincial Impact: Patients taking beta-blockers may have a transient increase in pulse and blood pressure when given GVOKE or GVOKE VialDx. Intervention The increase in blood pressure and heart rate may require therapy in patients with coronary artery disease. Insulin Clincial Impact: Insulin acts antagonistically to glucagon. Intervention Monitor blood glucose when GVOKE VialDx is used as a diagnostic aid in patients receiving insulin. Indomethacin Clincial Impact: In patients taking indomethacin, GVOKE may lose its ability to raise blood glucose or may even produce hypoglycemia. Intervention Monitor blood glucose levels during glucagon treatment of patients taking indomethacin. Anticholinergic Drugs Clincial Impact: The concomitant use of anticholinergic drugs and GVOKE VialDx increases the risk of gastrointestinal adverse reactions due to additive effects on inhibition of gastrointestinal motility. Intervention Concomitant use of anticholinergic drugs with GVOKE VialDx is not recommended. Warfarin Clincial Impact: GVOKE and GVOKE Vial Dx may increase the anticoagulant ef

Adverse Reactions

6 ADVERSE REACTIONS The following serious adverse reactions are described below and elsewhere in labeling: Substantial Increase in Blood Pressure in Patients with Pheochromocytoma [see Warnings and Precautions ( 5.1 )] . Hypoglycemia in Patients with Insulinoma [see Warnings and Precautions ( 5.2 )] . Serious Hypersensitivity Reactions [see Warnings and Precautions ( 5.3 )] Lack of Efficacy With Subcutaneous Use for Severe Hypoglycemia in Patients with Decreased Hepatic Glycogen [see Warnings and Precautions ( 5.4 )] Necrolytic Migratory Erythema [see Warnings and Precautions ( 5.5 )] . Hyperglycemia with Intravenous Use as a Diagnostic Aid in Patients with Diabetes Mellitus [see Warnings and Precautions ( 5.6 )] Blood Pressure and Heart Rate Increases with Intravenous Use as a Diagnostic Aid in Patients with Cardiac Disease [see Warnings and Precautions ( 5.7 )] Hypoglycemia in Patients with Glucagonoma with Intravenous Use as a Diagnostic Aid [see Warnings and Precautions ( 5.8 )] Most common adverse reactions (incidence 2% or greater) reported for GVOKE were: o Adults—nausea, vomiting, injection site edema raised 1 mm or greater, and headache ( 6.1 ) o Pediatric Patients—nausea,

Frequently Asked Questions

What is Gvoke HypoPen 0.5 mg Auto-Injector used for?

Gvoke HypoPen 0.5 mg Auto-Injector contains glucagon injection, solution. It is a injection, solution taken subcutaneous. Consult your doctor for specific uses.

Is Gvoke HypoPen 0.5 mg Auto-Injector a controlled substance?

Gvoke HypoPen 0.5 mg Auto-Injector is not classified as a controlled substance by the DEA.

What is the generic name for Gvoke HypoPen 0.5 mg Auto-Injector?

The generic name for Gvoke HypoPen 0.5 mg Auto-Injector is glucagon injection, solution. There are 3 other brand versions of glucagon injection, solution.

What is the NDC code for Gvoke HypoPen 0.5 mg Auto-Injector .5 mg/.1mL?

The NDC (National Drug Code) for Gvoke HypoPen 0.5 mg Auto-Injector .5 mg/.1mL is 72065-120, listed by Xeris Pharmaceuticals, Inc..

Product NDC

72065-120

Package NDC

72065-120-11

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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