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PRESCRIBING INFORMATION | IMPORTANT SAFETY INFORMATION YOU ARE INVITED TO A NATIONAL WEBINAR EVENT Evolving the Paradigm in Severe Management

SPEAKER: Davida F. Kruger, MSN, APN-BC, BC-ADM Certified Nurse Practitioner Henry Ford Health System Detroit, MI

WEBINAR DATE: Wednesday, February 24, 2021 6:30 PM ET

TO REGISTER, VISIT: www.HypoglycemiaManagement.com

Meeting Objectives

• Consider the serious issue of severe • Recognize administration challenges of hypoglycemia in , including its existing emergency kits and impact on affected individuals • Integrate the insights from today’s and their glycemic management presentation into an action plan for the • Discuss how emerging standards of care for identification and management of patients severe hypoglycemia can help overcome the at risk of severe hypoglycemia limitations of earlier guidelines

Please join us for a virtual event on Evolving the Paradigm in Severe Hypoglycemia Management. During this webinar we will focus on the objectives outlined above.

This event is not eligible for CME credit. This event complies with PhRMA guidelines. Attendance is limited to healthcare professionals.

Questions: Please contact POCN at [email protected] IMPORTANT SAFETY INFORMATION GVOKE is indicated for the treatment of severe hypoglycemia in adult and pediatric patients with diabetes ages 2 years and above.

Contraindications GVOKE is effective in treating hypoglycemia only GVOKE is contraindicated in patients with if sufficient hepatic glycogen is present. Patients pheochromocytoma, , and known in states of starvation, with hypersensitivity to glucagon or to any of the or chronic hypoglycemia, may not have excipients in GVOKE. Allergic reactions have been adequate levels of hepatic glycogen for GVOKE reported with glucagon and include anaphylactic administration to be effective. Patients with these with breathing difficulties and . conditions should be treated with glucose. Warnings and Precautions Necrolytic migratory erythema (NME), a skin rash commonly associated with , GVOKE is contraindicated in patients with has been reported postmarketing following pheochromocytoma because glucagon may continuous glucagon infusion and resolved stimulate the release of from with discontinuation of the glucagon. Should the tumor. If the patient develops a dramatic NME occur, consider whether the benefits increase in blood pressure and a previously of continuous glucagon infusion outweigh undiagnosed pheochromocytoma is suspected, 5 the risks. Glucagon administered to patients to 10 mg of mesylate, administered with may cause secondary intravenously, has been shown to be effective in hypoglycemia. lowering blood pressure. Adverse Reactions In patients with insulinoma, administration of glucagon may produce an initial increase in Most common (≥5%) adverse reactions blood glucose; however, GVOKE administration associated with GVOKE are , , may directly or indirectly (through an initial injection site edema (raised 1 mm or greater), rise in blood glucose) stimulate exaggerated and hypoglycemia. release from an insulinoma and cause Drug Interactions hypoglycemia. GVOKE is contraindicated in patients with insulinoma. If a patient develops Patients taking beta-blockers may have a symptoms of hypoglycemia after a dose of transient increase in pulse and blood pressure GVOKE, give glucose orally or intravenously. when given GVOKE. In patients taking indomethacin, GVOKE may lose its ability Allergic reactions have been reported with to raise blood glucose or may even produce glucagon. These include generalized rash, hypoglycemia. GVOKE may increase the and in some cases, anaphylactic shock with anticoagulant effect of warfarin. breathing difficulties and hypotension. GVOKE is contraindicated in patients with a prior Please see the Full Prescribing Information hypersensitivity reaction. for Gvoke HypoPen.

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