Does ONABOTULINUMTOXINA Cause Product quality issue? 549 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 549 reports of Product quality issue have been filed in association with ONABOTULINUMTOXINA. This represents 1.1% of all adverse event reports for ONABOTULINUMTOXINA.
549
Reports of Product quality issue with ONABOTULINUMTOXINA
1.1%
of all ONABOTULINUMTOXINA reports
13
Deaths
18
Hospitalizations
How Dangerous Is Product quality issue From ONABOTULINUMTOXINA?
Of the 549 reports, 13 (2.4%) resulted in death, 18 (3.3%) required hospitalization, and 13 (2.4%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ONABOTULINUMTOXINA. However, 549 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ONABOTULINUMTOXINA Alternatives Have Lower Product quality issue Risk?
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC
ONABOTULINUMTOXINA vs ONASEMNOGENE ABEPARVOVEC-XIOI
ONABOTULINUMTOXINA vs ONBREZ
ONABOTULINUMTOXINA vs ONDANSETRON
ONABOTULINUMTOXINA vs ONFI