29 reports of this reaction
1.9% of all CETYLPYRIDINIUM CHLORIDE reports
#8 most reported adverse reaction
SEPSIS is the #8 most commonly reported adverse reaction for CETYLPYRIDINIUM CHLORIDE, manufactured by RB Health (US) LLC. There are 29 FDA adverse event reports linking CETYLPYRIDINIUM CHLORIDE to SEPSIS. This represents approximately 1.9% of all 1,541 adverse event reports for this drug.
Patients taking CETYLPYRIDINIUM CHLORIDE who experience sepsis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SEPSIS is a less commonly reported adverse event for CETYLPYRIDINIUM CHLORIDE, but still significant enough to appear in the safety profile.
In addition to sepsis, the following adverse reactions have been reported for CETYLPYRIDINIUM CHLORIDE:
The following drugs have also been linked to sepsis in FDA adverse event reports:
SEPSIS has been reported as an adverse event in 29 FDA reports for CETYLPYRIDINIUM CHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEPSIS accounts for approximately 1.9% of all adverse event reports for CETYLPYRIDINIUM CHLORIDE, making it a notable side effect.
If you experience sepsis while taking CETYLPYRIDINIUM CHLORIDE, 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.