Does BIMEKIZUMAB-BKZX Cause Adverse event? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Adverse event have been filed in association with BIMEKIZUMAB-BKZX. This represents 0.7% of all adverse event reports for BIMEKIZUMAB-BKZX.
35
Reports of Adverse event with BIMEKIZUMAB-BKZX
0.7%
of all BIMEKIZUMAB-BKZX reports
1
Deaths
3
Hospitalizations
How Dangerous Is Adverse event From BIMEKIZUMAB-BKZX?
Of the 35 reports, 1 (2.9%) resulted in death, 3 (8.6%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIMEKIZUMAB-BKZX. However, 35 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 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 BIMEKIZUMAB-BKZX Alternatives Have Lower Adverse event Risk?
BIMEKIZUMAB-BKZX vs BINIMETINIB
BIMEKIZUMAB-BKZX vs BIOFLAVONOIDS
BIMEKIZUMAB-BKZX vs BIOTIN
BIMEKIZUMAB-BKZX vs BIPERIDEN
BIMEKIZUMAB-BKZX vs BIRCH TRITERPENES