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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BROLUCIZUMAB Cause Condition aggravated? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with BROLUCIZUMAB (BEOVU). This represents 1.6% of all adverse event reports for BROLUCIZUMAB.

11
Reports of Condition aggravated with BROLUCIZUMAB
1.6%
of all BROLUCIZUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From BROLUCIZUMAB?

Of the 11 reports, 1 (9.1%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BROLUCIZUMAB. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does BROLUCIZUMAB Cause?

Visual impairment (116) Vision blurred (106) Eye pain (81) Vitreous floaters (74) Vitritis (65) Ocular hyperaemia (62) Off label use (62) Subretinal fluid (62) Retinal vasculitis (52) Eye inflammation (50)

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 BROLUCIZUMAB Alternatives Have Lower Condition aggravated Risk?

BROLUCIZUMAB vs BROLUCIZUMAB-DBLL BROLUCIZUMAB vs BROMAZEPAM BROLUCIZUMAB vs BROMFENAC BROLUCIZUMAB vs BROMHEXINE BROLUCIZUMAB vs BROMOCRIPTINE

Related Pages

BROLUCIZUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated BROLUCIZUMAB Demographics