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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

PEGAPTANIB: 32 Adverse Event Reports & Safety Profile

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32
Total FAERS Reports
6 (18.8%)
Deaths Reported
2
Hospitalizations
32
As Primary/Secondary Suspect
2
Life-Threatening
1
Disabilities
Dec 17, 2004
FDA Approved
Discontinued
Status

Active Ingredient: PEGAPTANIB SODIUM · FDA Application: 021756 ·

First Report: 201302 · Latest Report: 20180510

What Are the Most Common PEGAPTANIB Side Effects?

#1 Most Reported
Off label use
8 reports (25.0%)
#2 Most Reported
Death
5 reports (15.6%)
#3 Most Reported
Ischaemic stroke
3 reports (9.4%)

All PEGAPTANIB Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Off label use 8 25.0% 0 0
Death 5 15.6% 5 0

Who Reports PEGAPTANIB Side Effects? Age & Gender Data

Gender: 60.9% female, 39.1% male. Average age: 73.3 years. Most reports from: US. View detailed demographics →

Is PEGAPTANIB Getting Safer? Reports by Year

YearReportsDeathsHosp.
2013 4 1 0
2014 1 1 1
2015 5 2 0
2017 2 0 0
2018 1 0 1

View full timeline →

What Is PEGAPTANIB Used For?

IndicationReports
Age-related macular degeneration 13
Neovascular age-related macular degeneration 7
Diabetic retinal oedema 5
Diabetic retinopathy 5

Official FDA Label for PEGAPTANIB

Official prescribing information from the FDA-approved drug label.