Does BOTULINUM TOXIN TYPE A Cause Therapy non-responder? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Therapy non-responder have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 1.7% of all adverse event reports for BOTULINUM TOXIN TYPE A.
64
Reports of Therapy non-responder with BOTULINUM TOXIN TYPE A
1.7%
of all BOTULINUM TOXIN TYPE A reports
61
Deaths
61
Hospitalizations
How Dangerous Is Therapy non-responder From BOTULINUM TOXIN TYPE A?
Of the 64 reports, 61 (95.3%) resulted in death, 61 (95.3%) required hospitalization, and 61 (95.3%) were considered life-threatening.
Is Therapy non-responder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 64 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 Therapy non-responder?
ETANERCEPT (3,472)
APREMILAST (3,360)
METHOTREXATE (2,965)
RITUXIMAB (2,731)
ADALIMUMAB (2,595)
PREDNISONE (2,563)
TREPROSTINIL (2,289)
INFLIXIMAB (2,122)
TOCILIZUMAB (1,775)
HYDROXYCHLOROQUINE (1,699)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Therapy non-responder 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