Does BOTULINUM TOXIN TYPE A Cause Intentional product misuse? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Intentional product misuse have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 0.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
19
Reports of Intentional product misuse with BOTULINUM TOXIN TYPE A
0.5%
of all BOTULINUM TOXIN TYPE A reports
11
Deaths
13
Hospitalizations
How Dangerous Is Intentional product misuse From BOTULINUM TOXIN TYPE A?
Of the 19 reports, 11 (57.9%) resulted in death, 13 (68.4%) required hospitalization, and 11 (57.9%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 19 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Intentional product misuse 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