Does BOTULINUM TOXIN TYPE A Cause Gait disturbance? 105 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 105 reports of Gait disturbance have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 2.8% of all adverse event reports for BOTULINUM TOXIN TYPE A.
105
Reports of Gait disturbance with BOTULINUM TOXIN TYPE A
2.8%
of all BOTULINUM TOXIN TYPE A reports
74
Deaths
94
Hospitalizations
How Dangerous Is Gait disturbance From BOTULINUM TOXIN TYPE A?
Of the 105 reports, 74 (70.5%) resulted in death, 94 (89.5%) required hospitalization, and 74 (70.5%) were considered life-threatening.
Is Gait disturbance Listed in the Official Label?
Yes, Gait disturbance 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 Gait disturbance?
DALFAMPRIDINE (8,780)
ADALIMUMAB (8,714)
ETANERCEPT (6,505)
METHOTREXATE (5,141)
TOFACITINIB (3,878)
PREGABALIN (3,590)
DIMETHYL (3,434)
SECUKINUMAB (3,222)
ABATACEPT (3,110)
LEFLUNOMIDE (3,041)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Gait disturbance 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