Does FLUOCINOLONE ACETONIDE Cause Product dose omission issue? 127 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 127 reports of Product dose omission issue have been filed in association with FLUOCINOLONE ACETONIDE (fluocinolone acetonide). This represents 7.2% of all adverse event reports for FLUOCINOLONE ACETONIDE.
127
Reports of Product dose omission issue with FLUOCINOLONE ACETONIDE
7.2%
of all FLUOCINOLONE ACETONIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From FLUOCINOLONE ACETONIDE?
Of the 127 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOCINOLONE ACETONIDE. However, 127 reports have been filed with the FAERS database.
What Other Side Effects Does FLUOCINOLONE ACETONIDE Cause?
Off label use (473)
Intraocular pressure increased (188)
Drug ineffective (141)
Device dislocation (137)
No adverse event (121)
Medical device removal (90)
Circumstance or information capable of leading to medication error (82)
Needle issue (72)
Device failure (66)
Product quality issue (59)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which FLUOCINOLONE ACETONIDE Alternatives Have Lower Product dose omission issue Risk?
FLUOCINOLONE ACETONIDE vs FLUOCINOLONE ACETONIDE\HYDROQUINONE\TRETINOIN
FLUOCINOLONE ACETONIDE vs FLUOCINONIDE
FLUOCINOLONE ACETONIDE vs FLUORESCEIN
FLUOCINOLONE ACETONIDE vs FLUOROMETHOLONE
FLUOCINOLONE ACETONIDE vs FLUOROURACIL