Does BOTULINUM TOXIN TYPE A Cause Adverse event? 92 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 92 reports of Adverse event have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 2.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
92
Reports of Adverse event with BOTULINUM TOXIN TYPE A
2.5%
of all BOTULINUM TOXIN TYPE A reports
84
Deaths
85
Hospitalizations
How Dangerous Is Adverse event From BOTULINUM TOXIN TYPE A?
Of the 92 reports, 84 (91.3%) resulted in death, 85 (92.4%) required hospitalization, and 85 (92.4%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for BOTULINUM TOXIN TYPE A.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Adverse event 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