197 reports of this reaction
2.4% of all POLYVINYL ALCOHOL, POVIDONE reports
#6 most reported adverse reaction
FATIGUE is the #6 most commonly reported adverse reaction for POLYVINYL ALCOHOL, POVIDONE, manufactured by Geri-Care Pharmaceuticals, Corp. There are 197 FDA adverse event reports linking POLYVINYL ALCOHOL, POVIDONE to FATIGUE. This represents approximately 2.4% of all 8,211 adverse event reports for this drug.
Patients taking POLYVINYL ALCOHOL, POVIDONE 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 POLYVINYL ALCOHOL, POVIDONE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for POLYVINYL ALCOHOL, POVIDONE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 197 FDA reports for POLYVINYL ALCOHOL, POVIDONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.4% of all adverse event reports for POLYVINYL ALCOHOL, POVIDONE, making it a notable side effect.
If you experience fatigue while taking POLYVINYL ALCOHOL, POVIDONE, 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.