6,061 reports of this reaction
3.2% of all FLUTICASONE PROPIONATE reports
#2 most reported adverse reaction
HEADACHE is the #2 most commonly reported adverse reaction for FLUTICASONE PROPIONATE, manufactured by Haleon US Holdings LLC. There are 6,061 FDA adverse event reports linking FLUTICASONE PROPIONATE to HEADACHE. This represents approximately 3.2% of all 187,924 adverse event reports for this drug.
Patients taking FLUTICASONE PROPIONATE who experience headache should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HEADACHE is moderately reported among FLUTICASONE PROPIONATE users, representing a notable but not dominant share of adverse events.
In addition to headache, the following adverse reactions have been reported for FLUTICASONE PROPIONATE:
The following drugs have also been linked to headache in FDA adverse event reports:
HEADACHE has been reported as an adverse event in 6,061 FDA reports for FLUTICASONE PROPIONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HEADACHE accounts for approximately 3.2% of all adverse event reports for FLUTICASONE PROPIONATE, making it one of the most commonly reported side effect.
If you experience headache 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.