10 reports of this reaction
2.0% of all WITCH HAZEL reports
#6 most reported adverse reaction
FATIGUE is the #6 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 FATIGUE. This represents approximately 2.0% of all 488 adverse event reports for this drug.
Patients taking WITCH HAZEL who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is a less commonly reported adverse event for WITCH HAZEL, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for WITCH HAZEL:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE 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.
FATIGUE accounts for approximately 2.0% of all adverse event reports for WITCH HAZEL, making it a notable side effect.
If you experience fatigue 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.