Does BOTULINUM TOXIN TYPE A Cause Pericarditis? 542 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 542 reports of Pericarditis have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 14.5% of all adverse event reports for BOTULINUM TOXIN TYPE A.
542
Reports of Pericarditis with BOTULINUM TOXIN TYPE A
14.5%
of all BOTULINUM TOXIN TYPE A reports
542
Deaths
488
Hospitalizations
How Dangerous Is Pericarditis From BOTULINUM TOXIN TYPE A?
Of the 542 reports, 542 (100.0%) resulted in death, 488 (90.0%) required hospitalization, and 498 (91.9%) were considered life-threatening.
Is Pericarditis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 542 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 Pericarditis?
METHOTREXATE (5,674)
CETIRIZINE (5,494)
ABATACEPT (5,385)
PREDNISONE (5,377)
RITUXIMAB (5,360)
TOCILIZUMAB (5,320)
ADALIMUMAB (5,303)
LEFLUNOMIDE (5,282)
INFLIXIMAB (5,231)
FOLIC ACID (5,153)
Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Pericarditis 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