Does BOTULINUM TOXIN TYPE A Cause Product quality issue? 412 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 412 reports of Product quality issue have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 11.0% of all adverse event reports for BOTULINUM TOXIN TYPE A.
412
Reports of Product quality issue with BOTULINUM TOXIN TYPE A
11.0%
of all BOTULINUM TOXIN TYPE A reports
408
Deaths
335
Hospitalizations
How Dangerous Is Product quality issue From BOTULINUM TOXIN TYPE A?
Of the 412 reports, 408 (99.0%) resulted in death, 335 (81.3%) required hospitalization, and 342 (83.0%) 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 BOTULINUM TOXIN TYPE A. However, 412 reports have been filed with the FAERS database.
What Other Side Effects Does BOTULINUM TOXIN TYPE A Cause?
Off label use (1,785)
Drug ineffective (1,175)
Drug intolerance (1,004)
Product use in unapproved indication (950)
Headache (797)
Migraine (775)
Maternal exposure during pregnancy (716)
Pain (714)
Hypoaesthesia (703)
Nausea (665)
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 BOTULINUM TOXIN TYPE A Alternatives Have Lower Product quality issue Risk?
BOTULINUM TOXIN TYPE A vs BREMELANOTIDE
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB
BOTULINUM TOXIN TYPE A vs BRENTUXIMAB VEDOTIN
BOTULINUM TOXIN TYPE A vs BREO ELLIPTA
BOTULINUM TOXIN TYPE A vs BREXANOLONE