1,275 reports of this reaction
3.0% of all SOLIFENACIN SUCCINATE reports
#4 most reported adverse reaction
FATIGUE is the #4 most commonly reported adverse reaction for SOLIFENACIN SUCCINATE, manufactured by Astellas Pharma US, Inc.. There are 1,275 FDA adverse event reports linking SOLIFENACIN SUCCINATE to FATIGUE. This represents approximately 3.0% of all 42,941 adverse event reports for this drug.
Patients taking SOLIFENACIN SUCCINATE 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 SOLIFENACIN SUCCINATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for SOLIFENACIN SUCCINATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 1,275 FDA reports for SOLIFENACIN SUCCINATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 3.0% of all adverse event reports for SOLIFENACIN SUCCINATE, making it a notable side effect.
If you experience fatigue while taking SOLIFENACIN SUCCINATE, 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.