Vizamyl Expanded Indications for Positron Emission Tomography Imaging and Quantification Overview
Join us for this live education event that will explore the recent FDA label expansion for Vizamyl and how it can impact clinical practice in Alzheimer’s disease diagnostics and treatment planning.
Webinar highlights:
Meet the Speaker:
Dr. Alexis Moscoso, Ph.D.
Chief Scientific Officer at ZRO Imaging
This event is intended for HealthCare Professionals only.
The event is sponsored by GE HealthCare.
The speaker will provide guidance based on their own practices and knowledge.
GE HealthCare and the speakers accept no responsibility for the use of guidance provided at this event.
Register Now
Vizamyl Important Safety Information
Product Indications and Use
VIZAMYL™ (flutemetamol F 18 injection) is indicated for positron-emission tomography (PET) of the brain to estimate amyloid beta neuritic plaque density in adults with cognitive impairment for:
Contraindications
VIZAMYL is contraindicated in patients with a history of hypersensitivity reaction to VIZAMYL or polysorbate 80.
Adverse Reactions
The most commonly reported adverse reactions in clinical trials were flushing (2 %), increased blood pressure (2 %), headache (1 %), nausea and dizziness (1 %). Postmarketing experience included anaphylactic reactions. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
To report SUSPECTED ADVERSE REACTIONS, contact GE HealthCare at 800 654 0118 (option 2 then option 1) or by email at [email protected] or FDA at 800 FDA 1088 or www.fda.gov/medwatch.
Access full updated Prescribing Information at https://gehealthcare.com/vizamyl-pi.
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September 2025 JB12408US