Does AFLIBERCEPT Cause Intentional dose omission? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Intentional dose omission have been filed in association with AFLIBERCEPT (EYLEA). This represents 0.4% of all adverse event reports for AFLIBERCEPT.
119
Reports of Intentional dose omission with AFLIBERCEPT
0.4%
of all AFLIBERCEPT reports
3
Deaths
12
Hospitalizations
How Dangerous Is Intentional dose omission From AFLIBERCEPT?
Of the 119 reports, 3 (2.5%) resulted in death, 12 (10.1%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AFLIBERCEPT. However, 119 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which AFLIBERCEPT Alternatives Have Lower Intentional dose omission Risk?
AFLIBERCEPT vs AGALSIDASE ALFA
AFLIBERCEPT vs AGALSIDASE BETA
AFLIBERCEPT vs AGOMELATINE
AFLIBERCEPT vs ALAWAY
AFLIBERCEPT vs ALBENDAZOLE