Does BRODALUMAB Cause Adverse event? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Adverse event have been filed in association with BRODALUMAB (Siliq). This represents 0.6% of all adverse event reports for BRODALUMAB.
12
Reports of Adverse event with BRODALUMAB
0.6%
of all BRODALUMAB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Adverse event From BRODALUMAB?
Of the 12 reports, 1 (8.3%) resulted in death, 1 (8.3%) required hospitalization.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for BRODALUMAB.
What Other Side Effects Does BRODALUMAB Cause?
Psoriasis (418)
Drug ineffective (177)
Arthralgia (175)
Fatigue (152)
Psoriatic arthropathy (141)
Intentional product use issue (136)
Headache (126)
Therapy interrupted (126)
Product dose omission issue (124)
Disease recurrence (118)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which BRODALUMAB Alternatives Have Lower Adverse event Risk?
BRODALUMAB vs BROLUCIZUMAB
BRODALUMAB vs BROLUCIZUMAB-DBLL
BRODALUMAB vs BROMAZEPAM
BRODALUMAB vs BROMFENAC
BRODALUMAB vs BROMHEXINE