150 reports of this reaction
2.3% of all FLUOCINOLONE ACETONIDE reports
#8 most reported adverse reaction
DEVICE FAILURE is the #8 most commonly reported adverse reaction for FLUOCINOLONE ACETONIDE, manufactured by ANI Pharmaceuticals, Inc.. There are 150 FDA adverse event reports linking FLUOCINOLONE ACETONIDE to DEVICE FAILURE. This represents approximately 2.3% of all 6,482 adverse event reports for this drug.
Patients taking FLUOCINOLONE ACETONIDE who experience device failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE FAILURE is a less commonly reported adverse event for FLUOCINOLONE ACETONIDE, but still significant enough to appear in the safety profile.
In addition to device failure, the following adverse reactions have been reported for FLUOCINOLONE ACETONIDE:
DEVICE FAILURE has been reported as an adverse event in 150 FDA reports for FLUOCINOLONE ACETONIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE FAILURE accounts for approximately 2.3% of all adverse event reports for FLUOCINOLONE ACETONIDE, making it a notable side effect.
If you experience device failure while taking FLUOCINOLONE ACETONIDE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.