Complete all sections carefully before your infusion appointment
1
Patient
2
Infusion
3
Medical
4
Screening
5
Consent
6
Sign
ℹ️
Before you beginThis form is specific to your Vyepti® (eptinezumab) infusion at NerveSync Neurology. Please have your current medication list available. Questions? Call 08 6243 0334.
1
Patient Details
Personal and contact information
Required
Required
Required
Required
Valid email required
Required
2
Vyepti® Infusion Details
Dose, appointment, and transport
Prescribed Dose
✓
100 mg
Standard dose
IV infusion over 30 min
✓
300 mg
High dose
IV infusion over 30 min
100 mg dose: One 100 mg vial diluted in 100 mL 0.9% NaCl, infused over 30 minutes via a 0.2 micron in-line filter. Minimum 30-minute observation post-infusion.
300 mg dose: Three 100 mg vials combined, diluted in 100 mL 0.9% NaCl, infused over 30 minutes via a 0.2 micron in-line filter. Minimum 30-minute observation post-infusion.
Please select your prescribed dose
Appointment
Required
Which cycle is this?
Transport
Required
You are advised not to drive for at least 30 minutes post-infusion. Discuss with your nurse if unsure.
3
Medical History
Allergies, medications, and health conditions
Allergies
Required (write "None" if none)
Previous Infusion Reactions
Current Medications
Required
General Health
Vyepti is not recommended during pregnancy. Discuss with your neurologist.
⚠️
Vyepti-specific screeningThese questions help assess your suitability and ensure safe administration of eptinezumab. Please answer honestly — your clinical team will review this before your infusion.
4
Vyepti Pre-Infusion Screening
CGRP history, prior biologics, and safety checks
Migraine History
Previous CGRP Therapy
Prior Biologic / Immunotherapy
Infections & Vaccination
An active infection may require postponement. Please notify clinic staff.
Day of Infusion
Fasting is not required. Hydration is encouraged.
5
Risks & Informed Consent
Please read carefully and tick each item
About Vyepti® (Eptinezumab)
Vyepti (eptinezumab) is a humanised monoclonal antibody targeting calcitonin gene-related peptide (CGRP), a molecule involved in migraine. It is administered by IV infusion every 3 months to prevent migraine in adults with episodic or chronic migraine.
Known Risks & Side Effects
Nasopharyngitis (cold-like symptoms) — most common
Urinary tract infection (reported in clinical trials)
All clinical staff are trained in anaphylaxis management. Emergency equipment including adrenaline, oxygen, and IV fluids is available at all times. You will be monitored for a minimum of 30 minutes after each infusion.
Informed Consent Declarations — Tick All Items
All 9 items must be ticked to proceed to the signature step.
Please tick all 9 consent items to continue
6
Declaration & Signature
Sign to confirm your informed consent
By signing below, I confirm that all information I have provided is accurate and complete to the best of my knowledge, and that I have read and agreed to all consent declarations above.
Required
Sign with your finger or mouse
Signature is required
❌ Submission failed. Please check your connection and try again, or call us on 08 6243 0334.
✓
Consent form complete
Review the summary below, then save or print
Vyepti® Infusion Consent
Ref: —
—
1. Patient Details
Full Name
Date of Birth
Phone
Email
Emergency Contact
Neurologist
2. Infusion Details
Prescribed Dose
Appointment Date
Infusion Number
Transport Home
3. Medical History
Drug Allergies
Other Allergies
Prev Vyepti Reaction
Prev IV Reaction
Current Medications
Pregnant / BF
Cardiac / Device
Other Conditions
4. Vyepti Pre-Infusion Screening
Migraine Type
Days / Month
Previous CGRP
Reason for Switch
Prior Biologic
Biologic Detail
Active Infection
Live Vaccine (4wks)
Vaccination Status
Alcohol (24hrs)
Eaten Today
Other Notes
5. Consent Declarations — All Confirmed ✓
✓Understands Vyepti® purpose, benefits, and method of administration.
✓Has had the opportunity to ask questions; satisfied with answers received.
✓Understands potential risks and side effects including rare risk of anaphylaxis.
✓Will remain at clinic for minimum 30-minute post-infusion observation period.
✓Will notify nursing staff immediately of any symptoms during or after infusion.
✓Understands Vyepti is administered every 3 months for optimal benefit.
✓Will inform neurologist if pregnant or breastfeeding before receiving Vyepti.
✓Understands the right to withdraw consent at any time without affecting ongoing care.
✓Consents to clinical information use under the Privacy Act 1988.
6. Signature & Declaration
Date Signed
Relationship
Patient / Guardian Signature
I confirm that all information provided in this form is accurate and complete to the best of my knowledge, and that I have read, understood, and agreed to all consent declarations above.
For clinic staff: Save this form as PDF and store in the patient's file. Vyepti® is a registered trademark of H. Lundbeck A/S.