Does BOTULINUM TOXIN TYPE A Cause Abdominal distension? 309 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 309 reports of Abdominal distension have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 8.3% of all adverse event reports for BOTULINUM TOXIN TYPE A.
309
Reports of Abdominal distension with BOTULINUM TOXIN TYPE A
8.3%
of all BOTULINUM TOXIN TYPE A reports
305
Deaths
305
Hospitalizations
How Dangerous Is Abdominal distension From BOTULINUM TOXIN TYPE A?
Of the 309 reports, 305 (98.7%) resulted in death, 305 (98.7%) required hospitalization, and 303 (98.1%) were considered life-threatening.
Is Abdominal distension Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 309 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 Abdominal distension?
ADALIMUMAB (3,728)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,238)
LEVONORGESTREL (1,700)
METHOTREXATE (1,471)
TREPROSTINIL (1,437)
PREDNISONE (1,429)
SEMAGLUTIDE (1,424)
VEDOLIZUMAB (1,411)
INFLIXIMAB (1,328)
POLYETHYLENE GLYCOL 3350 (1,158)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Abdominal distension 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