458 reports of this reaction
1.3% of all FLUTICASONE FUROATE reports
#19 most reported adverse reaction
WRONG TECHNIQUE IN DEVICE USAGE PROCESS is the #19 most commonly reported adverse reaction for FLUTICASONE FUROATE, manufactured by GlaxoSmithKline LLC. There are 458 FDA adverse event reports linking FLUTICASONE FUROATE to WRONG TECHNIQUE IN DEVICE USAGE PROCESS. This represents approximately 1.3% of all 35,585 adverse event reports for this drug.
Patients taking FLUTICASONE FUROATE who experience wrong technique in device usage process should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WRONG TECHNIQUE IN DEVICE USAGE PROCESS is a less commonly reported adverse event for FLUTICASONE FUROATE, but still significant enough to appear in the safety profile.
In addition to wrong technique in device usage process, the following adverse reactions have been reported for FLUTICASONE FUROATE:
The following drugs have also been linked to wrong technique in device usage process in FDA adverse event reports:
WRONG TECHNIQUE IN DEVICE USAGE PROCESS has been reported as an adverse event in 458 FDA reports for FLUTICASONE FUROATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG TECHNIQUE IN DEVICE USAGE PROCESS accounts for approximately 1.3% of all adverse event reports for FLUTICASONE FUROATE, making it a notable side effect.
If you experience wrong technique in device usage process while taking FLUTICASONE FUROATE, 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.