360 reports of this reaction
2.3% of all CEFDINIR reports
#7 most reported adverse reaction
RENAL FAILURE is the #7 most commonly reported adverse reaction for CEFDINIR, manufactured by American Health Packaging. There are 360 FDA adverse event reports linking CEFDINIR to RENAL FAILURE. This represents approximately 2.3% of all 15,428 adverse event reports for this drug.
Patients taking CEFDINIR who experience renal failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RENAL FAILURE is a less commonly reported adverse event for CEFDINIR, but still significant enough to appear in the safety profile.
In addition to renal failure, the following adverse reactions have been reported for CEFDINIR:
The following drugs have also been linked to renal failure in FDA adverse event reports:
RENAL FAILURE has been reported as an adverse event in 360 FDA reports for CEFDINIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
RENAL FAILURE accounts for approximately 2.3% of all adverse event reports for CEFDINIR, making it a notable side effect.
If you experience renal failure while taking CEFDINIR, 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.