10 reports of this reaction
2.0% of all WITCH HAZEL reports
#9 most reported adverse reaction
SINUSITIS is the #9 most commonly reported adverse reaction for WITCH HAZEL, manufactured by Haleon US Holdings LLC. There are 10 FDA adverse event reports linking WITCH HAZEL to SINUSITIS. This represents approximately 2.0% of all 488 adverse event reports for this drug.
Patients taking WITCH HAZEL 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 WITCH HAZEL, but still significant enough to appear in the safety profile.
In addition to sinusitis, the following adverse reactions have been reported for WITCH HAZEL:
The following drugs have also been linked to sinusitis in FDA adverse event reports:
SINUSITIS has been reported as an adverse event in 10 FDA reports for WITCH HAZEL. This does not prove causation, but indicates an association observed in post-market surveillance data.
SINUSITIS accounts for approximately 2.0% of all adverse event reports for WITCH HAZEL, making it a notable side effect.
If you experience sinusitis while taking WITCH HAZEL, 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.