Does BOTULINUM TOXIN TYPE A Cause Syncope? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Syncope 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.
18
Reports of Syncope with BOTULINUM TOXIN TYPE A
0.5%
of all BOTULINUM TOXIN TYPE A reports
0
Deaths
6
Hospitalizations
How Dangerous Is Syncope From BOTULINUM TOXIN TYPE A?
Of the 18 reports, 6 (33.3%) required hospitalization.
Is Syncope Listed in the Official Label?
Yes, Syncope 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 Syncope?
AMBRISENTAN (2,140)
TREPROSTINIL (1,908)
ADALIMUMAB (1,795)
FUROSEMIDE (1,431)
LENALIDOMIDE (1,280)
BISOPROLOL (1,279)
METOPROLOL (1,251)
AMLODIPINE (1,224)
ASPIRIN (1,193)
SACUBITRIL\VALSARTAN (1,163)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Syncope 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