How to locate and prescribe Emgality using the Electronic Media Record (EMR) system

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Search for “Emgality”

EMR screen icon

In the EMR system, select the formulation for your patient’s diagnosis1:

Recommended Dosing
National Drug Code (NDC)
Pen or Syringe Quantity
Recommended Dosing:
Emgality Pen 120 mg/mL SC injection
National Drug Code (NDC):
NDC 0002-1436-11
Pen or Syringe Quantity:
Qty: 1 per box
Recommended Dosing:
Emgality Syringe 120 mg/mL SC injection
National Drug Code (NDC):
NDC 0002-2377-11
Pen or Syringe Quantity:
Qty: 1 per box
Recommended Dosing:
Emgality Syringe 100 mg/mL SC injection
National Drug Code (NDC):
NDC 0002-3115-09
Pen or Syringe Quantity:
Qty: 3 per box

SC=subcutaneous.

Rx prescription icon

Prescribe the appropriate dose for your patient:

Emgality 120 mg for migraine

Loading Dose

(Use only if the patient does not begin treatment with a Loading Dose Kit [sample]c in the office)

Dispense: 2 pens or syringes at once with 0 refills

Maintenance Dose

(Use for all patients with migraine)

Dispense: 1 pen or syringe once monthly with 10 refills

cLoading Dose Kits (samples) are intended to establish tolerability and efficacy for a patient.

Emgality 300 mg for episodic cluster headache

Recommended Dose

Sig: 3 SC injections once monthly during an active cluster period

Dispense: (3) 100 mg prefilled syringes with 3 refills

SELECT IMPORTANT SAFETY INFORMATION

Hypersensitivity Reactions

Hypersensitivity reactions, including dyspnea, urticaria, and rash, have occurred with Emgality in clinical studies and the postmarketing setting. Cases of anaphylaxis and angioedema have also been reported in the postmarketing setting. If a serious or severe hypersensitivity reaction occurs, discontinue administration of Emgality and initiate appropriate therapy. Hypersensitivity reactions can occur days after administration and may be prolonged.

Discover how eligible patients can get Emgality for as little as $0 for up to 12 months.d Get patients started today.

dTerms and Conditions: Offer good until 12/31/2022 for up to 12 months of Emgality. Patients that have commercial drug insurance but do not have coverage for Emgality may be able to pay as little as $0 for their first fill of Emgality. Patients that have commercial drug insurance and have coverage for Emgality may be able to pay as little as $0 per fill. Offer subject to a monthly cap and a separate annual cap. Monthly and annual caps are set at Lilly's absolute discretion and may be changed by Lilly with or without notice. Participation in the program requires a valid patient HIPAA authorization. Patient is responsible for any applicable taxes, fees, or amounts exceeding monthly or annual caps. This offer is invalid for patients without commercial drug insurance or whose prescription claims for Emgality are eligible to be reimbursed, in whole or in part, by any governmental program, including, without limitation, Medicaid, Medicare, Medicare Part D, Medigap, DoD, VA, TRICARE®/CHAMPUS, or any state patient or pharmaceutical assistance program. Offer void where prohibited by law and subject to change or discontinue without notice. Card activation is required. Subject to additional terms and conditions, which can be found here.

References:

  1. Emgality [Prescribing Information]. Indianapolis, IN: Lilly USA, LLC.
  2. Data on File. Lilly USA, LLC. DOF-GZ-US-0085.
  3. Data on File. Lilly USA, LLC. DOF-GZ-US-0060.
  4. Data on File. Lilly USA, LLC. DOF-GZ-US-0071.

INDICATIONS

Emgality is a calcitonin gene-related peptide (CGRP) antagonist indicated in adults for the:

  • Preventive treatment of migraine
  • Treatment of episodic cluster headache

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS
Emgality is contraindicated in patients with serious hypersensitivity to galcanezumab-gnlm or to any of the excipients.

WARNINGS AND PRECAUTIONS
Hypersensitivity Reactions
Hypersensitivity reactions, including dyspnea, urticaria, and rash, have occurred with Emgality in clinical studies and the postmarketing setting. Cases of anaphylaxis and angioedema have also been reported in the postmarketing setting. If a serious or severe hypersensitivity reaction occurs, discontinue administration of Emgality and initiate appropriate therapy. Hypersensitivity reactions can occur days after administration and may be prolonged.

ADVERSE REACTIONS
The most common adverse reactions (incidence ≥2% and at least 2% greater than placebo) in Emgality clinical studies were injection site reactions.

Please see Full Prescribing Information, including Patient Information, for Emgality. See Instructions for Use included with the device.

GZ HCP ISI 10DEC2019