Does BOTULINUM TOXIN TYPE A Cause Prescribed underdose? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Prescribed underdose have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 2.1% of all adverse event reports for BOTULINUM TOXIN TYPE A.
78
Reports of Prescribed underdose with BOTULINUM TOXIN TYPE A
2.1%
of all BOTULINUM TOXIN TYPE A reports
78
Deaths
78
Hospitalizations
How Dangerous Is Prescribed underdose From BOTULINUM TOXIN TYPE A?
Of the 78 reports, 78 (100.0%) resulted in death, 78 (100.0%) required hospitalization, and 78 (100.0%) were considered life-threatening.
Is Prescribed underdose Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 78 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 Prescribed underdose?
NATALIZUMAB (2,162)
SACUBITRIL\VALSARTAN (1,864)
APIXABAN (1,469)
ABATACEPT (1,192)
PIMAVANSERIN (1,165)
FINGOLIMOD (1,114)
RITUXIMAB (1,067)
METHOTREXATE (1,066)
ADALIMUMAB (1,010)
TOCILIZUMAB (1,002)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Prescribed underdose 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