358 reports of this reaction
2.3% of all FEXOFENADINE HCL reports
#9 most reported adverse reaction
PRODUCT QUALITY ISSUE is the #9 most commonly reported adverse reaction for FEXOFENADINE HCL, manufactured by CVS Pharmacy. There are 358 FDA adverse event reports linking FEXOFENADINE HCL to PRODUCT QUALITY ISSUE. This represents approximately 2.3% of all 15,768 adverse event reports for this drug.
Patients taking FEXOFENADINE HCL who experience product quality issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT QUALITY ISSUE is a less commonly reported adverse event for FEXOFENADINE HCL, but still significant enough to appear in the safety profile.
In addition to product quality issue, the following adverse reactions have been reported for FEXOFENADINE HCL:
The following drugs have also been linked to product quality issue in FDA adverse event reports:
PRODUCT QUALITY ISSUE has been reported as an adverse event in 358 FDA reports for FEXOFENADINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT QUALITY ISSUE accounts for approximately 2.3% of all adverse event reports for FEXOFENADINE HCL, making it a notable side effect.
If you experience product quality issue while taking FEXOFENADINE HCL, 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.