Does TRIAMCINOLONE ACETONIDE\ZINC Cause Product use in unapproved indication? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use in unapproved indication have been filed in association with TRIAMCINOLONE ACETONIDE\ZINC. This represents 45.5% of all adverse event reports for TRIAMCINOLONE ACETONIDE\ZINC.
5
Reports of Product use in unapproved indication with TRIAMCINOLONE ACETONIDE\ZINC
45.5%
of all TRIAMCINOLONE ACETONIDE\ZINC reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use in unapproved indication From TRIAMCINOLONE ACETONIDE\ZINC?
Of the 5 reports, 1 (20.0%) resulted in death, 1 (20.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
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 TRIAMCINOLONE ACETONIDE\ZINC. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does TRIAMCINOLONE ACETONIDE\ZINC Cause?
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)