1,927 reports of this reaction
1.7% of all CHLORHEXIDINE GLUCONATE reports
#1 most reported adverse reaction
FATIGUE is the #1 most commonly reported adverse reaction for CHLORHEXIDINE GLUCONATE, manufactured by Rising Pharma Holdings, Inc.. There are 1,927 FDA adverse event reports linking CHLORHEXIDINE GLUCONATE to FATIGUE. This represents approximately 1.7% of all 110,211 adverse event reports for this drug.
Patients taking CHLORHEXIDINE GLUCONATE 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 CHLORHEXIDINE GLUCONATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for CHLORHEXIDINE GLUCONATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,927 FDA reports for CHLORHEXIDINE GLUCONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 1.7% of all adverse event reports for CHLORHEXIDINE GLUCONATE, making it one of the most commonly reported side effect.
If you experience fatigue while taking CHLORHEXIDINE GLUCONATE, 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.