Does BOTULINUM TOXIN TYPE A Cause Dyskinesia? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Dyskinesia have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 0.4% of all adverse event reports for BOTULINUM TOXIN TYPE A.
15
Reports of Dyskinesia with BOTULINUM TOXIN TYPE A
0.4%
of all BOTULINUM TOXIN TYPE A reports
0
Deaths
4
Hospitalizations
How Dangerous Is Dyskinesia From BOTULINUM TOXIN TYPE A?
Of the 15 reports, 4 (26.7%) required hospitalization.
Is Dyskinesia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 15 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 Dyskinesia?
CARBIDOPA\LEVODOPA (5,368)
QUETIAPINE (1,529)
ARIPIPRAZOLE (1,496)
RISPERIDONE (1,363)
OLANZAPINE (1,060)
CLOZAPINE (890)
PALIPERIDONE (794)
LURASIDONE (791)
VALBENAZINE (772)
SERTRALINE (597)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Dyskinesia 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