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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 NOS Cause Product use issue? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product use issue have been filed in association with BOTULINUM TOXIN NOS. This represents 4.0% of all adverse event reports for BOTULINUM TOXIN NOS.

11
Reports of Product use issue with BOTULINUM TOXIN NOS
4.0%
of all BOTULINUM TOXIN NOS reports
6
Deaths
7
Hospitalizations

How Dangerous Is Product use issue From BOTULINUM TOXIN NOS?

Of the 11 reports, 6 (54.5%) resulted in death, 7 (63.6%) required hospitalization, and 6 (54.5%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BOTULINUM TOXIN NOS. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does BOTULINUM TOXIN NOS Cause?

Drug ineffective (99) Off label use (75) Product use in unapproved indication (44) Migraine (40) Treatment failure (39) Headache (33) Nausea (32) Sedation (29) Drug intolerance (28) Pain (26)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which BOTULINUM TOXIN NOS Alternatives Have Lower Product use issue Risk?

BOTULINUM TOXIN NOS vs BOTULINUM TOXIN TYPE A BOTULINUM TOXIN NOS vs BREMELANOTIDE BOTULINUM TOXIN NOS vs BRENTUXIMAB BOTULINUM TOXIN NOS vs BRENTUXIMAB VEDOTIN BOTULINUM TOXIN NOS vs BREO ELLIPTA

Related Pages

BOTULINUM TOXIN NOS Full Profile All Product use issue Reports All Drugs Causing Product use issue BOTULINUM TOXIN NOS Demographics