Does BIMEKIZUMAB-BKZX Cause Device malfunction? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Device malfunction have been filed in association with BIMEKIZUMAB-BKZX. This represents 1.2% of all adverse event reports for BIMEKIZUMAB-BKZX.
64
Reports of Device malfunction with BIMEKIZUMAB-BKZX
1.2%
of all BIMEKIZUMAB-BKZX reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device malfunction From BIMEKIZUMAB-BKZX?
Of the 64 reports, 1 (1.6%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIMEKIZUMAB-BKZX. However, 64 reports have been filed with the FAERS database.
What Other Side Effects Does BIMEKIZUMAB-BKZX Cause?
Product dose omission issue (694)
Psoriasis (621)
Drug ineffective (402)
Product availability issue (364)
Off label use (335)
Psoriatic arthropathy (301)
Injection site pain (263)
Therapy interrupted (252)
Hidradenitis (233)
Inappropriate schedule of product administration (214)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which BIMEKIZUMAB-BKZX Alternatives Have Lower Device malfunction Risk?
BIMEKIZUMAB-BKZX vs BINIMETINIB
BIMEKIZUMAB-BKZX vs BIOFLAVONOIDS
BIMEKIZUMAB-BKZX vs BIOTIN
BIMEKIZUMAB-BKZX vs BIPERIDEN
BIMEKIZUMAB-BKZX vs BIRCH TRITERPENES