Does BROLUCIZUMAB-DBLL Cause Conjunctival hyperaemia? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Conjunctival hyperaemia have been filed in association with BROLUCIZUMAB-DBLL. This represents 1.3% of all adverse event reports for BROLUCIZUMAB-DBLL.
36
Reports of Conjunctival hyperaemia with BROLUCIZUMAB-DBLL
1.3%
of all BROLUCIZUMAB-DBLL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Conjunctival hyperaemia From BROLUCIZUMAB-DBLL?
Of the 36 reports, 1 (2.8%) required hospitalization.
Is Conjunctival hyperaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BROLUCIZUMAB-DBLL. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does BROLUCIZUMAB-DBLL Cause?
Vitreous floaters (479)
Visual impairment (446)
Vision blurred (416)
Eye inflammation (387)
Visual acuity reduced (365)
Retinal vasculitis (323)
Uveitis (305)
Vitritis (284)
Eye pain (234)
Vitreous opacities (205)
What Other Drugs Cause Conjunctival hyperaemia?
NETARSUDIL (240)
LAMOTRIGINE (120)
LATANOPROST\NETARSUDIL (98)
IBUPROFEN (95)
ACETAMINOPHEN (67)
DUPILUMAB (66)
DICLOFENAC (51)
BEVACIZUMAB (50)
RITUXIMAB (50)
DEXAMETHASONE\TOBRAMYCIN (44)
Which BROLUCIZUMAB-DBLL Alternatives Have Lower Conjunctival hyperaemia Risk?
BROLUCIZUMAB-DBLL vs BROMAZEPAM
BROLUCIZUMAB-DBLL vs BROMFENAC
BROLUCIZUMAB-DBLL vs BROMHEXINE
BROLUCIZUMAB-DBLL vs BROMOCRIPTINE
BROLUCIZUMAB-DBLL vs BROTIZOLAM