Does AFLIBERCEPT Cause Ocular hyperaemia? 367 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 367 reports of Ocular hyperaemia have been filed in association with AFLIBERCEPT (EYLEA). This represents 1.4% of all adverse event reports for AFLIBERCEPT.
367
Reports of Ocular hyperaemia with AFLIBERCEPT
1.4%
of all AFLIBERCEPT reports
2
Deaths
37
Hospitalizations
How Dangerous Is Ocular hyperaemia From AFLIBERCEPT?
Of the 367 reports, 2 (0.5%) resulted in death, 37 (10.1%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Ocular hyperaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AFLIBERCEPT. However, 367 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 Ocular hyperaemia?
DUPILUMAB (6,938)
CYCLOSPORINE (1,508)
BIMATOPROST (1,447)
CENEGERMIN-BKBJ (1,226)
BRIMONIDINE (917)
ADALIMUMAB (714)
LATANOPROST (587)
DORZOLAMIDE\TIMOLOL (581)
LIFITEGRAST (570)
TRAVOPROST (478)
Which AFLIBERCEPT Alternatives Have Lower Ocular hyperaemia Risk?
AFLIBERCEPT vs AGALSIDASE ALFA
AFLIBERCEPT vs AGALSIDASE BETA
AFLIBERCEPT vs AGOMELATINE
AFLIBERCEPT vs ALAWAY
AFLIBERCEPT vs ALBENDAZOLE