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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.

RANIBIZUMAB-EQRN: 97 Adverse Event Reports & Safety Profile

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97
Total FAERS Reports
6 (6.2%)
Deaths Reported
0
Hospitalizations
97
As Primary/Secondary Suspect
Prescription
Status

FDA Application: 761165 ·

First Report: 20230426 · Latest Report: 20250107

What Are the Most Common RANIBIZUMAB-EQRN Side Effects?

#1 Most Reported
Product administration error
13 reports (13.4%)
#2 Most Reported
Product contamination
9 reports (9.3%)
#3 Most Reported
Product storage error
8 reports (8.2%)

All RANIBIZUMAB-EQRN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Product administration error 13 13.4% 0 0
Product contamination 9 9.3% 0 0
Product storage error 8 8.3% 0 0
Circumstance or information capable of leading to medication error 7 7.2% 0 0
Visual impairment 7 7.2% 0 0
Death 6 6.2% 6 0
Drug ineffective 6 6.2% 0 0
Product use issue 6 6.2% 0 0
Vision blurred 5 5.2% 0 0

Who Reports RANIBIZUMAB-EQRN Side Effects? Age & Gender Data

Gender: 75.0% female, 25.0% male. Average age: 85.6 years. Most reports from: US. View detailed demographics →

Is RANIBIZUMAB-EQRN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2023 14 3 0
2024 44 2 0
2025 4 0 0

View full timeline →

What Is RANIBIZUMAB-EQRN Used For?

IndicationReports
Product used for unknown indication 72
Neovascular age-related macular degeneration 11
Macular degeneration 6

Official FDA Label for RANIBIZUMAB-EQRN

Official prescribing information from the FDA-approved drug label.