Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Florbetapir
Drug ID BADD_D00906
Description Florbetapir (18F) is a radiopharmaceutical compound containing the radionuclide fluorine-18 bound to the compound florbetapir, a molecule that binds with high affinity to beta amyloid plaque, a peptide that plays a key role in Alzheimer's Disease pathogenesis. Marketed as the product Amyvid, florbetapir 18F is indicated for positron emission tomography (PET) imaging of the brain to estimate β-amyloid neuritic plaque density in adult patients with cognitive impairment who are being evaluated for Alzheimer's Disease (AD) and other causes of cognitive decline. The radionucleide fluorine-18 was chosen as it has a half life of 110 minutes allowing it to accumulate sufficiently in the brain before undergoing positon emission decay.
Indications and Usage Florbetapir 18F is indicated for Positron Emission Tomography (PET) imaging of the brain to estimate β-amyloid neuritic plaque density in adult patients with cognitive impairment who are being evaluated for Alzheimer's Disease (AD) and other causes of cognitive decline.
Marketing Status Prescription; Discontinued
ATC Code V09AX05
DrugBank ID DB09149
KEGG ID D09617
MeSH ID C545186
PubChem ID 57396865
TTD Drug ID Not Available
NDC Product Code Not Available
Synonyms florbetapir | 2-(2-(2-(2-fluoroethoxy)ethoxy)ethoxy)-5-(4-methylaminostyryl)pyridine | 4-(2-(6-(2-(2-(2-fluoroethoxy)ethoxy)ethoxy)pyridin-3-yl)vinyl)-N-methylbenzamide | Amyvid | 18F-AV-45 | florbetapir F 18 | florbetapir F18
Chemical Information
Molecular Formula C20H25FN2O3
CAS Registry Number 938435-69-9
SMILES CNC1=CC=C(C=C1)C=CC2=CN=C(C=C2)OCCOCCOCCF
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Dysgeusia17.02.07.003; 07.14.03.001--
Flushing08.01.03.025; 24.03.01.002; 23.06.05.003--
Gastrointestinal disorder07.11.01.001--Not Available
Headache17.14.01.001--
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
Injection site irritation08.02.03.027; 12.07.03.027--Not Available
Injection site pain12.07.03.011; 08.02.03.010--Not Available
Injection site reaction12.07.03.015; 08.02.03.014--
Nausea07.01.07.001--
Neoplasm malignant16.16.01.001--Not Available
Nervous system disorder17.02.10.001--Not Available
Pruritus23.03.12.001--
Skin disorder23.03.03.007--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Angiopathy24.03.02.007--Not Available
Infusion site rash23.03.13.018; 12.07.05.017; 08.02.05.017--Not Available
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