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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BIMEKIZUMAB Cause Device malfunction? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Device malfunction have been filed in association with BIMEKIZUMAB (Bimzelx). This represents 0.5% of all adverse event reports for BIMEKIZUMAB.

11
Reports of Device malfunction with BIMEKIZUMAB
0.5%
of all BIMEKIZUMAB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device malfunction From BIMEKIZUMAB?

Of the 11 reports.

Is Device malfunction Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BIMEKIZUMAB. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does BIMEKIZUMAB Cause?

Psoriatic arthropathy (615) Psoriasis (400) Drug ineffective (293) Inappropriate schedule of product administration (238) Injection site pain (225) Product dose omission issue (163) Off label use (160) Oral candidiasis (146) Fatigue (138) Therapy interrupted (138)

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 Alternatives Have Lower Device malfunction Risk?

BIMEKIZUMAB vs BIMEKIZUMAB-BKZX BIMEKIZUMAB vs BINIMETINIB BIMEKIZUMAB vs BIOFLAVONOIDS BIMEKIZUMAB vs BIOTIN BIMEKIZUMAB vs BIPERIDEN

Related Pages

BIMEKIZUMAB Full Profile All Device malfunction Reports All Drugs Causing Device malfunction BIMEKIZUMAB Demographics