Does TRIAMCINOLONE ACETONIDE Cause Incorrect product administration duration? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Incorrect product administration duration have been filed in association with TRIAMCINOLONE ACETONIDE (Triamcinolone Acetonide). This represents 0.5% of all adverse event reports for TRIAMCINOLONE ACETONIDE.
91
Reports of Incorrect product administration duration with TRIAMCINOLONE ACETONIDE
0.5%
of all TRIAMCINOLONE ACETONIDE reports
64
Deaths
69
Hospitalizations
How Dangerous Is Incorrect product administration duration From TRIAMCINOLONE ACETONIDE?
Of the 91 reports, 64 (70.3%) resulted in death, 69 (75.8%) required hospitalization, and 69 (75.8%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIAMCINOLONE ACETONIDE. However, 91 reports have been filed with the FAERS database.
What Other Side Effects Does TRIAMCINOLONE ACETONIDE Cause?
Drug ineffective (4,498)
Off label use (2,034)
Pain (1,349)
Condition aggravated (1,187)
Nausea (1,186)
Vomiting (1,142)
Headache (1,103)
Synovitis (1,085)
Rash (1,082)
Product use in unapproved indication (1,046)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TRIAMCINOLONE ACETONIDE Alternatives Have Lower Incorrect product administration duration Risk?
TRIAMCINOLONE ACETONIDE vs TRIAMCINOLONE HEXACETONIDE
TRIAMCINOLONE ACETONIDE vs TRIAMTERENE
TRIAMCINOLONE ACETONIDE vs TRIATEC
TRIAMCINOLONE ACETONIDE vs TRIAZOLAM
TRIAMCINOLONE ACETONIDE vs TRICHLORMETHIAZIDE