Does BOTULINUM TOXIN TYPE A Cause Duodenal ulcer perforation? 510 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 510 reports of Duodenal ulcer perforation have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 13.6% of all adverse event reports for BOTULINUM TOXIN TYPE A.
510
Reports of Duodenal ulcer perforation with BOTULINUM TOXIN TYPE A
13.6%
of all BOTULINUM TOXIN TYPE A reports
510
Deaths
422
Hospitalizations
How Dangerous Is Duodenal ulcer perforation From BOTULINUM TOXIN TYPE A?
Of the 510 reports, 510 (100.0%) resulted in death, 422 (82.7%) required hospitalization, and 432 (84.7%) were considered life-threatening.
Is Duodenal ulcer perforation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 510 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 Duodenal ulcer perforation?
METHOTREXATE (4,239)
LEFLUNOMIDE (4,200)
FOLIC ACID (4,152)
ABATACEPT (4,147)
TOCILIZUMAB (4,130)
DICLOFENAC (4,120)
CETIRIZINE (4,117)
DESOXIMETASONE (4,084)
RITUXIMAB (4,081)
PREDNISONE (4,060)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Duodenal ulcer perforation 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