Does AFLIBERCEPT Cause Condition aggravated? 161 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 161 reports of Condition aggravated have been filed in association with AFLIBERCEPT (EYLEA). This represents 0.6% of all adverse event reports for AFLIBERCEPT.
161
Reports of Condition aggravated with AFLIBERCEPT
0.6%
of all AFLIBERCEPT reports
4
Deaths
22
Hospitalizations
How Dangerous Is Condition aggravated From AFLIBERCEPT?
Of the 161 reports, 4 (2.5%) resulted in death, 22 (13.7%) required hospitalization, and 2 (1.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AFLIBERCEPT. However, 161 reports have been filed with the FAERS database.
What Other Side Effects Does AFLIBERCEPT Cause?
Death (7,669)
Visual impairment (1,836)
Blindness (1,337)
Endophthalmitis (1,289)
Off label use (1,156)
Eye pain (1,057)
Product dose omission issue (1,051)
Blindness unilateral (1,012)
Vision blurred (1,012)
Visual acuity reduced (993)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which AFLIBERCEPT Alternatives Have Lower Condition aggravated Risk?
AFLIBERCEPT vs AGALSIDASE ALFA
AFLIBERCEPT vs AGALSIDASE BETA
AFLIBERCEPT vs AGOMELATINE
AFLIBERCEPT vs ALAWAY
AFLIBERCEPT vs ALBENDAZOLE