36 reports of this reaction
1.9% of all CEFPODOXIME PROXETIL reports
#9 most reported adverse reaction
ASTHENIA is the #9 most commonly reported adverse reaction for CEFPODOXIME PROXETIL, manufactured by Amici Pharmaceuticals, LLC.. There are 36 FDA adverse event reports linking CEFPODOXIME PROXETIL to ASTHENIA. This represents approximately 1.9% of all 1,861 adverse event reports for this drug.
Patients taking CEFPODOXIME PROXETIL who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for CEFPODOXIME PROXETIL, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for CEFPODOXIME PROXETIL:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 36 FDA reports for CEFPODOXIME PROXETIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 1.9% of all adverse event reports for CEFPODOXIME PROXETIL, making it a notable side effect.
If you experience asthenia while taking CEFPODOXIME PROXETIL, 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.