Does BRODALUMAB Cause Extra dose administered? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Extra dose administered have been filed in association with BRODALUMAB (Siliq). This represents 0.4% of all adverse event reports for BRODALUMAB.
9
Reports of Extra dose administered with BRODALUMAB
0.4%
of all BRODALUMAB reports
1
Deaths
3
Hospitalizations
How Dangerous Is Extra dose administered From BRODALUMAB?
Of the 9 reports, 1 (11.1%) resulted in death, 3 (33.3%) required hospitalization.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRODALUMAB. However, 9 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 Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which BRODALUMAB Alternatives Have Lower Extra dose administered Risk?
BRODALUMAB vs BROLUCIZUMAB
BRODALUMAB vs BROLUCIZUMAB-DBLL
BRODALUMAB vs BROMAZEPAM
BRODALUMAB vs BROMFENAC
BRODALUMAB vs BROMHEXINE