Does BIMEKIZUMAB-BKZX Cause Extra dose administered? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Extra dose administered have been filed in association with BIMEKIZUMAB-BKZX. This represents 0.1% of all adverse event reports for BIMEKIZUMAB-BKZX.
5
Reports of Extra dose administered with BIMEKIZUMAB-BKZX
0.1%
of all BIMEKIZUMAB-BKZX reports
0
Deaths
0
Hospitalizations
How Dangerous Is Extra dose administered From BIMEKIZUMAB-BKZX?
Of the 5 reports.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BIMEKIZUMAB-BKZX. However, 5 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 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 BIMEKIZUMAB-BKZX Alternatives Have Lower Extra dose administered Risk?
BIMEKIZUMAB-BKZX vs BINIMETINIB
BIMEKIZUMAB-BKZX vs BIOFLAVONOIDS
BIMEKIZUMAB-BKZX vs BIOTIN
BIMEKIZUMAB-BKZX vs BIPERIDEN
BIMEKIZUMAB-BKZX vs BIRCH TRITERPENES