252 reports of this reaction
2.0% of all LORATADINE AND PSEUDOEPHEDRINE SULFATE reports
#9 most reported adverse reaction
FATIGUE is the #9 most commonly reported adverse reaction for LORATADINE AND PSEUDOEPHEDRINE SULFATE, manufactured by Bayer HealthCare LLC.. There are 252 FDA adverse event reports linking LORATADINE AND PSEUDOEPHEDRINE SULFATE to FATIGUE. This represents approximately 2.0% of all 12,600 adverse event reports for this drug.
Patients taking LORATADINE AND PSEUDOEPHEDRINE SULFATE 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 LORATADINE AND PSEUDOEPHEDRINE SULFATE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for LORATADINE AND PSEUDOEPHEDRINE SULFATE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 252 FDA reports for LORATADINE AND PSEUDOEPHEDRINE SULFATE. 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 LORATADINE AND PSEUDOEPHEDRINE SULFATE, making it a notable side effect.
If you experience fatigue while taking LORATADINE AND PSEUDOEPHEDRINE SULFATE, 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.