Does ONABOTULINUMTOXINA Cause Product label issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product label issue have been filed in association with ONABOTULINUMTOXINA. This represents 0.0% of all adverse event reports for ONABOTULINUMTOXINA.
18
Reports of Product label issue with ONABOTULINUMTOXINA
0.0%
of all ONABOTULINUMTOXINA reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product label issue From ONABOTULINUMTOXINA?
Of the 18 reports, 3 (16.7%) required hospitalization, and 2 (11.1%) were considered life-threatening.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does ONABOTULINUMTOXINA Cause?
Drug ineffective (18,179)
Off label use (9,698)
Product preparation error (3,593)
Multiple use of single-use product (2,781)
Therapeutic response decreased (2,685)
Headache (2,316)
Injection site pain (2,143)
Eyelid ptosis (1,853)
Wrong technique in product usage process (1,477)
Migraine (1,232)
What Other Drugs Cause Product label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
Which ONABOTULINUMTOXINA Alternatives Have Lower Product label issue Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI