Does ONABOTULINUMTOXINA Cause Product storage error? 651 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 651 reports of Product storage error have been filed in association with ONABOTULINUMTOXINA. This represents 1.3% of all adverse event reports for ONABOTULINUMTOXINA.
651
Reports of Product storage error with ONABOTULINUMTOXINA
1.3%
of all ONABOTULINUMTOXINA reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product storage error From ONABOTULINUMTOXINA?
Of the 651 reports, 3 (0.5%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 651 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ONABOTULINUMTOXINA Alternatives Have Lower Product storage error Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI