4,114 reports of this reaction
2.2% of all FLUTICASONE PROPIONATE reports
#8 most reported adverse reaction
OFF LABEL USE is the #8 most commonly reported adverse reaction for FLUTICASONE PROPIONATE, manufactured by Haleon US Holdings LLC. There are 4,114 FDA adverse event reports linking FLUTICASONE PROPIONATE to OFF LABEL USE. This represents approximately 2.2% of all 187,924 adverse event reports for this drug.
Patients taking FLUTICASONE PROPIONATE who experience off label use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OFF LABEL USE is a less commonly reported adverse event for FLUTICASONE PROPIONATE, but still significant enough to appear in the safety profile.
In addition to off label use, the following adverse reactions have been reported for FLUTICASONE PROPIONATE:
The following drugs have also been linked to off label use in FDA adverse event reports:
OFF LABEL USE has been reported as an adverse event in 4,114 FDA reports for FLUTICASONE PROPIONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OFF LABEL USE accounts for approximately 2.2% of all adverse event reports for FLUTICASONE PROPIONATE, making it a notable side effect.
If you experience off label use while taking FLUTICASONE PROPIONATE, 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.