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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-BKZX Cause Therapy interrupted? 252 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 252 reports of Therapy interrupted have been filed in association with BIMEKIZUMAB-BKZX. This represents 4.7% of all adverse event reports for BIMEKIZUMAB-BKZX.

252
Reports of Therapy interrupted with BIMEKIZUMAB-BKZX
4.7%
of all BIMEKIZUMAB-BKZX reports
0
Deaths
15
Hospitalizations

How Dangerous Is Therapy interrupted From BIMEKIZUMAB-BKZX?

Of the 252 reports, 15 (6.0%) required hospitalization.

Is Therapy interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BIMEKIZUMAB-BKZX. However, 252 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) Hidradenitis (233) Inappropriate schedule of product administration (214) Incorrect dose administered (209)

What Other Drugs Cause Therapy interrupted?

ADALIMUMAB (5,755) ETANERCEPT (3,397) RELUGOLIX (3,251) CERTOLIZUMAB PEGOL (3,209) LENALIDOMIDE (2,724) UPADACITINIB (1,741) ABATACEPT (1,726) CLOZAPINE (1,722) AMIKACIN (1,283) TOFACITINIB (1,182)

Which BIMEKIZUMAB-BKZX Alternatives Have Lower Therapy interrupted Risk?

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

Related Pages

BIMEKIZUMAB-BKZX Full Profile All Therapy interrupted Reports All Drugs Causing Therapy interrupted BIMEKIZUMAB-BKZX Demographics