Does BOTULINUM TOXIN TYPE A Cause Adverse reaction? 267 Reports in FDA Database

According to the FDA Adverse Event Reporting System (FAERS), 267 reports of Adverse reaction have been filed in association with BOTULINUM TOXIN TYPE A (Jeuveau). This represents 7.1% of all adverse event reports for BOTULINUM TOXIN TYPE A.

How Dangerous Is Adverse reaction From BOTULINUM TOXIN TYPE A?

Of the 267 reports, 267 (100.0%) resulted in death, 266 (99.6%) required hospitalization, and 266 (99.6%) were considered life-threatening.

Is Adverse reaction Listed in the Official Label?

Yes, Adverse reaction is listed as a known adverse reaction in the official FDA drug label for BOTULINUM TOXIN TYPE A.

What Other Side Effects Does BOTULINUM TOXIN TYPE A Cause?

What Other Drugs Cause Adverse reaction?

Which BOTULINUM TOXIN TYPE A Alternatives Have Lower Adverse reaction Risk?

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