Does ONABOTULINUMTOXINA Cause Product preparation error? 3,593 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,593 reports of Product preparation error have been filed in association with ONABOTULINUMTOXINA. This represents 7.3% of all adverse event reports for ONABOTULINUMTOXINA.
3,593
Reports of Product preparation error with ONABOTULINUMTOXINA
7.3%
of all ONABOTULINUMTOXINA reports
1
Deaths
14
Hospitalizations
How Dangerous Is Product preparation error From ONABOTULINUMTOXINA?
Of the 3,593 reports, 1 (0.0%) resulted in death, 14 (0.4%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 3,593 reports have been filed with the FAERS database.
What Other Side Effects Does ONABOTULINUMTOXINA Cause?
Drug ineffective (18,179)
Off label use (9,698)
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)
Death (1,153)
What Other Drugs Cause Product preparation error?
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which ONABOTULINUMTOXINA Alternatives Have Lower Product preparation error Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI