Does AFLIBERCEPT Cause Product dose omission? 201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Product dose omission have been filed in association with AFLIBERCEPT (EYLEA). This represents 0.8% of all adverse event reports for AFLIBERCEPT.
201
Reports of Product dose omission with AFLIBERCEPT
0.8%
of all AFLIBERCEPT reports
10
Deaths
22
Hospitalizations
How Dangerous Is Product dose omission From AFLIBERCEPT?
Of the 201 reports, 10 (5.0%) resulted in death, 22 (10.9%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AFLIBERCEPT. However, 201 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which AFLIBERCEPT Alternatives Have Lower Product dose omission Risk?
AFLIBERCEPT vs AGALSIDASE ALFA
AFLIBERCEPT vs AGALSIDASE BETA
AFLIBERCEPT vs AGOMELATINE
AFLIBERCEPT vs ALAWAY
AFLIBERCEPT vs ALBENDAZOLE