Does HEXETIDINE Cause Product use in unapproved indication? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product use in unapproved indication have been filed in association with HEXETIDINE. This represents 35.1% of all adverse event reports for HEXETIDINE.
13
Reports of Product use in unapproved indication with HEXETIDINE
35.1%
of all HEXETIDINE reports
13
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From HEXETIDINE?
Of the 13 reports, 13 (100.0%) resulted in death.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HEXETIDINE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does HEXETIDINE Cause?
Toxic epidermal necrolysis (16)
Overdose (12)
Toxicity to various agents (12)
Bezoar (10)
Completed suicide (10)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)