1,884 reports of this reaction
1.9% of all BURN RELIEF reports
#8 most reported adverse reaction
SINUSITIS is the #8 most commonly reported adverse reaction for BURN RELIEF, manufactured by Actavis Pharma, Inc.. There are 1,884 FDA adverse event reports linking BURN RELIEF to SINUSITIS. This represents approximately 1.9% of all 98,034 adverse event reports for this drug.
Patients taking BURN RELIEF who experience sinusitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SINUSITIS is a less commonly reported adverse event for BURN RELIEF, but still significant enough to appear in the safety profile.
In addition to sinusitis, the following adverse reactions have been reported for BURN RELIEF:
The following drugs have also been linked to sinusitis in FDA adverse event reports:
SINUSITIS has been reported as an adverse event in 1,884 FDA reports for BURN RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
SINUSITIS accounts for approximately 1.9% of all adverse event reports for BURN RELIEF, making it a notable side effect.
If you experience sinusitis while taking BURN RELIEF, 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.