Does BOTULINUM TOXIN TYPE A Cause No adverse event? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of No adverse event have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 1.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
55
Reports of No adverse event with BOTULINUM TOXIN TYPE A
1.5%
of all BOTULINUM TOXIN TYPE A reports
45
Deaths
45
Hospitalizations
How Dangerous Is No adverse event From BOTULINUM TOXIN TYPE A?
Of the 55 reports, 45 (81.8%) resulted in death, 45 (81.8%) required hospitalization, and 45 (81.8%) were considered life-threatening.
Is No adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 55 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 No adverse event?
OMALIZUMAB (9,736)
ALBUTEROL (8,971)
ETONOGESTREL (8,827)
TOCILIZUMAB (6,492)
RITUXIMAB (5,915)
METHYLPHENIDATE (4,197)
MOMETASONE FUROATE (3,717)
HUMAN IMMUNOGLOBULIN G (3,064)
ETHINYL ESTRADIOL\NORELGESTROMIN (3,014)
VEDOLIZUMAB (2,477)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower No 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