142 reports of this reaction
1.5% of all ALLANTOIN reports
#16 most reported adverse reaction
SEPSIS is the #16 most commonly reported adverse reaction for ALLANTOIN, manufactured by Skinfix, Inc.. There are 142 FDA adverse event reports linking ALLANTOIN to SEPSIS. This represents approximately 1.5% of all 9,609 adverse event reports for this drug.
Patients taking ALLANTOIN 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 ALLANTOIN, but still significant enough to appear in the safety profile.
In addition to sepsis, the following adverse reactions have been reported for ALLANTOIN:
The following drugs have also been linked to sepsis in FDA adverse event reports:
SEPSIS has been reported as an adverse event in 142 FDA reports for ALLANTOIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEPSIS accounts for approximately 1.5% of all adverse event reports for ALLANTOIN, making it a notable side effect.
If you experience sepsis while taking ALLANTOIN, 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.