349 reports of this reaction
2.3% of all CEFDINIR reports
#8 most reported adverse reaction
SINUSITIS is the #8 most commonly reported adverse reaction for CEFDINIR, manufactured by American Health Packaging. There are 349 FDA adverse event reports linking CEFDINIR to SINUSITIS. This represents approximately 2.3% of all 15,428 adverse event reports for this drug.
Patients taking CEFDINIR who experience sinusitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SINUSITIS is a less commonly reported adverse event for CEFDINIR, but still significant enough to appear in the safety profile.
In addition to sinusitis, the following adverse reactions have been reported for CEFDINIR:
The following drugs have also been linked to sinusitis in FDA adverse event reports:
SINUSITIS has been reported as an adverse event in 349 FDA reports for CEFDINIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
SINUSITIS accounts for approximately 2.3% of all adverse event reports for CEFDINIR, making it a notable side effect.
If you experience sinusitis 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.