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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BOTULINUM TOXIN TYPE A Cause Medication error? 69 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Medication error have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 1.8% of all adverse event reports for BOTULINUM TOXIN TYPE A.

69
Reports of Medication error with BOTULINUM TOXIN TYPE A
1.8%
of all BOTULINUM TOXIN TYPE A reports
55
Deaths
58
Hospitalizations

How Dangerous Is Medication error From BOTULINUM TOXIN TYPE A?

Of the 69 reports, 55 (79.7%) resulted in death, 58 (84.1%) required hospitalization, and 57 (82.6%) were considered life-threatening.

Is Medication error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN TYPE A. However, 69 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 Medication error?

ACETAMINOPHEN (1,809) METHOTREXATE (1,269) OXYCODONE (1,058) ADALIMUMAB (954) DICLOFENAC (915) TOCILIZUMAB (907) RITUXIMAB (902) NAPROXEN (883) INFLIXIMAB (868) PREDNISONE (856)

Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Medication error 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

Related Pages

BOTULINUM TOXIN TYPE A Full Profile All Medication error Reports All Drugs Causing Medication error BOTULINUM TOXIN TYPE A Demographics