Does ONABOTULINUMTOXINA Cause Product administration error? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Product administration error have been filed in association with ONABOTULINUMTOXINA. This represents 0.1% of all adverse event reports for ONABOTULINUMTOXINA.
51
Reports of Product administration error with ONABOTULINUMTOXINA
0.1%
of all ONABOTULINUMTOXINA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From ONABOTULINUMTOXINA?
Of the 51 reports, 2 (3.9%) required hospitalization, and 1 (2.0%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 51 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ONABOTULINUMTOXINA Alternatives Have Lower Product administration error Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI