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What is Amyvid
Approved as Treatment by the FDA
Florbetapir (18F), also known as Amyvid, is approved by the FDA for 3 uses including Alzheimer's Disease (AD) and Positron Emission Tomography .Effectiveness
When to interrupt dosage
The sum of Amyvid depends upon the identified condition. The measure of dosage fluctuates, in keeping with the delivery technique stated in the accompanying table.Warnings
There are 20 known major drug interactions with Amyvid.Amyvid Novel Uses: Which Conditions Have a Clinical Trial Featuring Amyvid?
41 active investigations are being conducted to assess the utility of Amyvid in Positron Emission Tomography imaging.Patient Q&A Section about amyvid
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.What is amyvid used for?
"Use of Amyvid in these patients is indicated to help rule out AD and to provide an indication of the density of β-amyloid neuritic plaques."
Is amyvid FDA approved?
"The FDA has approved Amyvid™ (florbetapir F 18 injection) for use in patients being evaluated for Alzheimer's disease and other causes of cognitive decline. Amyvid is a radioactive diagnostic agent that is injected into a vein and scans the brain for amyloid plaques. The presence of amyloid plaques is one marker for Alzheimer's disease."
Who owns amyvid?
"Indianapolis, IN: Avid Radiopharmaceuticals Inc; March 2012.[2]
Amyvid is a trademark of Eli Lilly and Company. Amyvid is a radioactive diagnostic agent used to measure amyloid plaques in the brain. Avid Radiopharmaceuticals Inc manufactures Amyvid."
When was amyvid FDA approved?
"The approval date for this document is 4/6/2012. The date of this document is 5/3/2012."