1,480 reports of this reaction
2.0% of all PIOGLITAZONE reports
#7 most reported adverse reaction
FATIGUE is the #7 most commonly reported adverse reaction for PIOGLITAZONE, manufactured by Takeda Pharmaceuticals America, Inc.. There are 1,480 FDA adverse event reports linking PIOGLITAZONE to FATIGUE. This represents approximately 2.0% of all 74,368 adverse event reports for this drug.
PIOGLITAZONE has an overall safety score of 85 out of 100. Patients taking PIOGLITAZONE 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 PIOGLITAZONE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for PIOGLITAZONE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,480 FDA reports for PIOGLITAZONE. 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 PIOGLITAZONE, making it a notable side effect.
If you experience fatigue while taking PIOGLITAZONE, 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.