Does BRODALUMAB Cause Intentional dose omission? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Intentional dose omission have been filed in association with BRODALUMAB (Siliq). This represents 2.4% of all adverse event reports for BRODALUMAB.
50
Reports of Intentional dose omission with BRODALUMAB
2.4%
of all BRODALUMAB reports
2
Deaths
19
Hospitalizations
How Dangerous Is Intentional dose omission From BRODALUMAB?
Of the 50 reports, 2 (4.0%) resulted in death, 19 (38.0%) required hospitalization, and 2 (4.0%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRODALUMAB. However, 50 reports have been filed with the FAERS database.
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 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 BRODALUMAB Alternatives Have Lower Intentional dose omission Risk?
BRODALUMAB vs BROLUCIZUMAB
BRODALUMAB vs BROLUCIZUMAB-DBLL
BRODALUMAB vs BROMAZEPAM
BRODALUMAB vs BROMFENAC
BRODALUMAB vs BROMHEXINE